CN1323354A - 用双链rna抑制鉴定基因功能 - Google Patents

用双链rna抑制鉴定基因功能 Download PDF

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CN1323354A
CN1323354A CN99810196A CN99810196A CN1323354A CN 1323354 A CN1323354 A CN 1323354A CN 99810196 A CN99810196 A CN 99810196A CN 99810196 A CN99810196 A CN 99810196A CN 1323354 A CN1323354 A CN 1323354A
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CN1198938C (zh
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G·普莱廷克
C·普拉托伊夫
K·莫蒂尔
T·波格尔特
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Abstract

提供负责在细胞中赋予特定表型的DNA的鉴定方法,所述方法包括:a)以相应于启动子、当合适的转录因子结合于所述启动子时能够启动从所述cDNA或DNA转录出双链(ds)RNA的方向,在合适的载体中构建所述细胞DNA的cDNA文库或基因组文库,b)将所述文库引入包含所述转录因子的一种或多种所述细胞中,且c)鉴定和分离包含所述文库的特定表型的所述细胞,并鉴定所述文库中负责赋予所述表型的DNA或cDNA片段。采用该技术,可以将功能确定到已知DNA序列,方法为:a)鉴定细胞中所述DNA序列的同源物,b)从所述细胞中分离出相关的DNA同源物或其片段,c)将所述同源物或其片段以相应于合适启动子、当合适的转录因子结合于所述启动子时能够启动从所述DNA同源物或其片段转化dsRNA的方向,克隆到合适的载体中,d)将所述载体引入得自步骤a)的包含所述转录因子的所述细胞中。

Description

用双链RNA抑制鉴定基因功能
本发明涉及采用双链RNA抑制(dsRNAi)来特征鉴定或鉴定基因的功能,涉及鉴定负责在细胞中诱导特定表型的DNA的方法以及将功能确定到已知基因序列的方法。
最近,在Nature第391卷,第806-811页(1998年2月)中已经描述了:将双链RNA引入到细胞中,导致有效且特异性地干扰细胞中内源基因的表达,并且这种干扰比在反义技术中提出的单独提供任一RNA链要有效得多。也发现当将所述RNA引入到线虫Caenorhabditiselegans(C.celegans)蠕虫基因组或体腔中时,在这种蠕虫中存在该基因活性的这种特异性降低。
本发明人已经利用了这种技术,并应用其进一步设计新的发明方法,以将功能确定至已经在各种计划诸如人类基因组计划中测序、并且还给予了一种特定功能的基因或DNA片段上,并且将其用于鉴定负责赋予特定表型的DNA。
因此,按照本发明的第一个方面,提供一种鉴定负责在细胞中赋予表型的DNA的方法,所述方法包括:a)以相应于启动子的方向,构建所述细胞DNA的cNDA文库或基因组文库,使得在合适的转录因子结合于所述启动子时能够促进从所述cDNA或DNA转录出双链(ds)RNA,b)将所述文库引入到包含所述转录因子的一种或多种所述细胞中,且c)鉴定并分离包含所述文库的所需表型的所述细胞,并鉴定所述文库中负责赋予所述表型的DNA或cDNA片段。
在本发明的一个优选实施方案中,在步骤b)之前,可以将所述文库组成为如在所提供的实施例中更详细描述的等级库,以致包括例如基因家族。
按照本发明的再一方面,也提供一种将功能确定到已知DNA序列的方法,所述方法包括a)鉴定细胞中所述DNA的同源物,b)从所述细胞中分离出相关的DNA同源物或其片段,c)以相应于合适的转录因子结合于启动子时能够促进dsRNA转录的启动子的方向,将所述同源物或片段克隆到合适的载体中,d)将所述载体引入到得自步骤a)的包含所述转录因子的所述细胞中,以及e)鉴定与野生型相比所述细胞的表型。
在本发明的每一方面,均可以以相应于具有以上所定义特性的单个启动子的有义和反义方向提供所述核苷酸序列或DNA序列,或者可选择地,可以在两个相同启动子之间提供所述核苷酸序列或DNA序列。在这两个实施方案中,在启动子结合其合适的转录因子后,由所述启动子启动的转录提供dsRNA。
按照本发明的细胞可以得自一种生物或包含于一种生物中。在所述细胞包含于一种生物中的场合下,可以改变所述生物以表达合适的转录因子。所述生物可以为植物、动物、真菌或酵母中的任何一种,但最好可以是线虫蠕虫C.elegans,它可以是C.elegans野生型、nuc-1或pha-ts突变体中的任何一种或所述突变的组合。在一个替代实施方案中,可以便利地将所述DNA或cDNA文库或所述DNA同源物或其片段转染或转化到可以饲喂给所述生物的微生物中,诸如细菌或酵母细胞,所述生物最好是线虫蠕虫C.elegans。在本发明的该实施方案中,可以将所述微生物改变以表达所述合适的转录因子。所述微生物最好是大肠杆菌。
在本发明的每个方面,可以在包含编码所述转录因子的核苷酸序列的合适的DNA载体中,构建所述DNA文库、DNA同源物或DNA片段。或者,可以由另一载体编码所述转录因子。在再一替代方法中,所述细胞或生物可以表达所述转录因子,或者可以将其改变以表达所述转录因子。最好是,用于按照本发明的方法中的任一所述载体包含一种选择标记,可以例如为编码sup-35或其片段的核苷酸序列。可以将所述核苷酸序列相应于启动子定向,以致转录因子结合至所述启动子而启动从所述DNA转录出双链RNA。图10图解了使得在C.elegans中能够产生双链RNA的载体和DNA序列的方向。因此,在一个实施方案中,所述DNA位于载体上的两个启动子之间,当合适的转录因子结合于所述启动子时,所述载体能够表达dsRNA。或者,所述载体包含两个拷贝的所述DNA序列,所述两个拷贝以相应于所述启动子的有义和反义方向组织,而且当所述标记包含于pha-1突变C.elegans中时,所述标记为可选择的。所述启动子最好是T7、T3或SP6启动子中的任一种,所述转录因子包括所述合适的聚合酶。
所述选择标记最好包含能够在所述细胞中抑制或防止基因表达的核苷酸序列,而且所述基因负责赋予已知的表型。该核苷酸序列可以是赋予所述表型的所述基因的一部分,或与所述基因相同,而所述核苷酸序列本身的定向与在合适的转录因子结合于所述启动子时能够启动双链RNA转录的合适启动子的定向相应。或者,所述核苷酸序列可以是赋予所述表型的所述基因序列的一部分,或与所述基因序列相同,而所述核苷酸序列是这样的序列,以致允许所述合适的载体或另一载体通过同源重组整合到所述细胞的基因组中,并且在所述整合后,所述核苷酸序列能够抑制赋予所述表型的所述基因序列的表达。在该实施方案中,所述核苷酸序列包含足以防止所述核苷酸序列在其整合到所述基因组中之后进行翻译的终止密码子。
有利地是,在所述方法中,可以将化合物加到所述细胞上或生物中,以便筛选所需表型,诸如当与野生型相比时,具有对该化合物的抗性或敏感性。所述启动子最好是诱导型的。在某些实施方案中,所述转录因子可以得自噬菌体,诸如为由噬菌体启动子驱动的T7聚合酶。然而,当利用C.elegan时,可以使用蠕虫特异性或组织特异性启动子,例如Let858、SERCA、UL6、myo-2或myo-3。所述大肠杆菌菌株最好是RNA酶Ⅲ阴性菌株,甚至更优选为RNA酶阴性菌株。
本发明的再一方面提供一种产生包含一种外源转录因子和一种转基因的非人类转基因生物的方法,其中所述转基因包含一个有效连接至DNA片段的启动子,当所述转录因子结合于所述启动子时表达所述DNA片段;所述方法包括:a)提供包含第一构成物的第一转基因生物和包含第二构成物的第二转基因生物,所述第一构成物掺入了编码外源转录因子的DNA,而所述第二构成物包括至少一个有效连接至所需DNA序列的启动子,在所述第一转基因生物的转录因子结合于所述启动子时,表达所述所需DNA序列,b)将所述第一转基因生物与所述第二转基因生物杂交,并选择表达所述所需DNA序列的后代。在一个实施方案中,通过将所述第一和第二构成物转化到相应的微生物中,随后用所述微生物饲喂所述相应的生物,产生所述第一和第二转基因生物。最好是,所述第二构成物包含所述所需DNA序列,所述所需DNA序列相应于所述启动子的方向,使得当所述转录因子结合于所述启动子时,能够启动从所述DNA转录出dsRNA。在该实施方案中,所述第二构成物包含两个邻接所述所需DNA序列的启动子,所述启动子在所述转录因子与其结合时,可以启动从所述DNA序列转录出dsRNA。或者,以相应于所述启动子的有义和反义的方向提供所述DNA序列,使得可以在所述转录因子结合于所述启动子时产生dsRNA。在这些实施方案中的每一个中,可能最好为所述第一构成物和/或第二构成物提供一个有效连接至启动子的报道基因,所述启动子在所述转录因子与其结合时能够启动所述报道基因的转录。最好是,所述报道基因编码荧光素酶、绿荧光蛋白、β半乳糖苷酶或β-内酰胺酶中的任一个。
本发明也包括在酵母双杂种载体实验中所鉴定的克隆的验证方法,所述实验是本领域技术人员众所周知的,并且所述实验由Chien等(1991)首先提出,用于探测蛋白-蛋白相互作用。按照本发明的方法包括:提供一种构成物,所述构成物包含在双杂种载体实验中所鉴定的蛋白的编码DNA,所述构成物使得以相应于一个或多个启动子的方向提供所述DNA,所述启动子在合适的转录因子结合于所述启动子时,能够促进从所述DNA转录出双链RNA;用所述构成物转化诸如细菌细胞的细胞,或者转化包含所述转录因子的生物;并且与野生型相比,鉴定在所述细胞或生物中的表型变化,所述生物可以是C.elegan或诸如此类的生物。最好是,所述转录因子在所述细胞或生物中为可诱导的。如上所述,可以再一次将所述DNA序列定位于两种启动子之间,或以相对于单一启动子的有义和反义两个方向定位。最好是,所述启动子为噬菌体聚合酶启动子,而所述转录因子为RNA聚合酶,最好是T7聚合酶。本发明的范围也包括用于转化所述细胞或生物的载体以及所述细胞或生物本身。
在本发明的再一方面,提供减轻植物害虫侵染的方法,所述方法包括:a)从所述害虫中鉴定出或者对于其生存、生长、增殖或者对于其生殖重要的DNA序列,b)在合适的载体中,以相对于一个或多个启动子的方向克隆得自步骤a)的所述序列或其片段,所述启动子在合适的转录因子与其结合时能够从所述序列转录出RNA或dsRNA,并且c)将所述载体引入到所述植物中。
因此,有利的是,按照本发明的方法提供一种特别具有选择性的机制,用于减轻害虫侵染,而且在某些情况下用于减轻植物寄生虫侵染,使得当所述害虫在所述植物上摄食时,它将摄入植物中所表达的dsRNA,因此抑制对于害虫生长、生存、增殖或生殖重要的DNA在害虫中的表达。在一个优选实施方案中,所述害虫可以为小垫刃线虫属物种(Tylenchulus ssp.)、穿孔线虫属物种(Radopholus ssp.)、细杆滑刃线虫属物种(Rhadinaphelenchus ssp.)、异皮线虫属物种(Heteroderassp.)、小盘旋线虫属物种(Rotylenchulus,ssp.)、短体线虫属物种(Pratylenchus ssp.)、刺线虫属物种(Belonolaimus ssp.)、Canjanus ssp.、根结线虫属物种(Meloidogyne ssp.)、球异皮线虫属物种(Globoderassp.)、科布线虫属物种(Nacobbus ssp.)、茎线虫属物种(Ditylenchusssp.)、滑刃线虫属物种(Aphelenchoides ssp.)、潜根线虫属物种(Hirschmenniella ssp.)、鳗线虫属物种(Anguina ssp.)、纽带线虫属物种(Hoplolaimus ssp.)、螺旋线虫属物种(Heliotylenchus ssp.)、小环线虫属物种(Criconemella ssp.)、剑线虫属物种(Xiphinema ssp.)、长针线虫属物种(Longidorus ssp.)、毛刺线虫属物种(Trichodorus ssp.)、副毛刺线虫属物种(Paratrichodorus ssp.)、真滑刃线虫属物种(Aphelenchs ssp.)中的任何一种。可以将按照本发明该方面的DNA序列或其片段克隆在两个组织特异性启动子之间,诸如在两个根特异性启动予之间。
本发明的再一方面涉及用于本发明每个方法中用于构建所述文库的载体,所述载体包含两个相同的启动子,所述启动子的定向使得在合适的转录因子结合于所述启动子时,所述启动子能够启动从位于所述启动子之间的DNA序列转录出dsRNA。所述DNA序列可以例如包括一个多克隆位点。最好是,所述表达载体包含一段编码选择标记的核苷酸序列。在一个实施方案中,编码所述选择标记的所述核苷酸序列位于两个相同的启动子之间,所述启动子的定向使得在合适的转录因子结合于所述启动子时,所述启动子能够启动从位于所述启动子之间的DNA转录出双链RNA。为了引入到具有pha-1突变的C.elegans中,所述选择标记最好包含一段编码sup-35的核苷酸序列。
最好是,所述转录因子或者包括一个结合于其相应启动子的噬菌体聚合酶,或者包括一个C.elegans特异性启动子,甚至更优选T7聚合酶。最好是,所述载体包含一个在所述相同的启动子之间的多克隆位点。
在本发明的再一方面,提供一种表达载体,用于表达供按照本发明方法使用的合适的转录因子,所述载体包含一段有效连接至合适的表达控制序列的、编码所述转录因子的核苷酸序列。所述表达控制序列最好包括启动子,所述启动子为诱导型启动子、组成型启动子、普遍性启动子或组织特异性启动子或它们的组合。最好是所述转录因子包括噬菌体聚合酶,最好为T7、T3或SP6的RNA聚合酶。
本发明的再一方面提供一个选择系统,用于鉴定用按照本发明的载体对细胞或生物的转化,所述系统包括一个按照本发明的载体,其中所述选择标记包括一段在所述细胞或生物中能够抑制或防止负责赋予已知表型的基因表达的核苷酸序列。所述核苷酸序列最好对应于赋予所述已知表型的所述基因的一部分,或与所述基因相同,而且所述核苷酸序列本身位于两个相同启动子之间,所述启动子在合适的转录因子与其结合时,能够启动双链RNA的转录。或者,所述核苷酸序列包含的一段核苷酸序列是赋予所述细胞或生物已知表型的所述基因序列的一部分,或与所述基因相同,并且使得在所述载体通过同源重组而整合到所述细胞或生物的染色体中之后,所述序列抑制赋予所述已知表型的所述基因序列的表达。最好是,按照该实施方案,所述核苷酸序列包含足以防止所述核苷酸序列在整合到所述染色体之后进行翻译的终止密码子。所述已知基因序列最好包含可选择的sup-35基因或其片段,可通过鉴定将其引入到pha-1 et123ts突变型C.elegans蠕虫中之后于高于25℃的温度下生长的后代,可选择出该基因或片段。
在本发明的再一方面,提供所述已知基因的序列,所述序列包括通过鉴定将所述载体引入到pha-1 et123ts突变型C.elegans蠕虫中之后后代在高于25℃的温度下生长可选择出的sup-35基因或其片段。又一个方面包括将功能确定至多细胞生物的DNA序列的方法,所述方法包括:a)在能够从所述启动子启动子转录的多细胞生物中,提供ⅰ)构成物,所述构成物包含在所述多细胞生物中能够促进转录的两个启动子之间克隆的所述DNA片段;b)与野生型相比,鉴定所述多细胞生物的表型。
参考附图,通过以下仅为示例性的实施例,可以更清楚地理解本发明,在附图中:
图1是按照本发明的质粒PGN1的核苷酸序列。
图2是按照本发明的质粒PGN100的核苷酸序列。
图3是按照本发明的方法中使用的质粒和转化方案的示意图。
图4是按照本发明使用的表达载体的说明。
图5是用于转化C.elegans的T7RNA聚合酶表达载体的示意图。
图6是质粒PGN1的图解。
图7是用于dsRBA抑制、编码sup-35dsRNA的增强载体的图示说明。
图8是用于整合到C.elegans基因组中的载体的说明。
图9是相对于从所述DNA序列启动dsRNA表达的合适启动子的DNA序列位置的说明。
图10是质粒pGN108的说明。
图11是质粒pGN105的说明。
图12是质粒pGN400的说明。
图13是质粒pGN401的说明。
图14是质粒pGN110的说明。
图15是具有正向和反向T7/T3/SP6启动子的质粒pAS2的说明。
图16是具有正向和反向T7/T3/SP6启动子的质粒pGAD424的说明。
图17是质粒pAS2-cyh2-HA+both T7-final的说明。
图18为质粒pGAD424-without-FULL-ICE-BOTH-T7的说明。
图19(a)为质粒pGN205的说明,而(b)为质粒pGN207的说明。
实施例A:有序等级汇集的cDNA文库的构建及其应用
随机有序和汇集的文库:
所述载体为一种大肠杆菌载体,带有两个T7启动子,在所述两个启动子之间有一个多克隆位点(MCS)。所述两个启动子彼此相对地定向并朝向所述MCS定向。在存在在大肠杆菌、C.elegans或任何其它生物中表达的T7RNA聚合酶的情况下,将从所述两个T7启动子开始,产生RNA。由于这些启动子以相反的方向定向,因此将从插入(或克隆)到位于所述两个启动子之间的MCS中的DNA,产生两条RNA链,当T7RNA聚合酶与启动子结合时,导致产生双链RNA(dsRNA)。
采用标准分子生物学技术,在所述MCS中构建了一个C.eleganscDNA文库。将所述文库转化到大肠杆菌中,让所产生的大肠杆菌在在培养基中生长并贮存在96孔多孔板中。在该阶段,可以分离质粒DNA并将其对应于大肠杆菌菌落的96多孔板贮存在96孔多孔板中。记录了大约100,000个菌落。以这种方式,该文库将含有约5倍于总的表达的C.elegans cDNA变异的cDNA变异,这为低表达序列出现在该文库中提供了机会。这将产生约1041块96孔板。必要时将所述板进行等级汇集。目前,将所述克隆的汇集范围安排在10-100个。如果按每8个或每12个进行等级汇集(因为96孔板具有8排12列,则这些数字更为方便),则这产生大约87块多孔板,大约8352个孔。如果按96孔即整个板进行等级汇集,则这产生约11块板,大约1041个孔。在等级汇集的任一阶段,均可以分离质粒DNA,当使用较少的板时,工作量可能较少,但将导致复杂度的降低,尽管在按12列汇集的条件下不应该是这种情况。也可以用所述原始DNA进行所述DNA的汇集。
以下实验描述了应该如何对所述DNA文库以及对大肠杆菌文库进行等级汇集。
用于RNAi技术的、含有C.elegans基因组中每个基因的有序文库及其应用
由于基因组测序计划即将进入尾声,因而可以将这种信息用于T7RNA抑制技术的应用中。采用PCR技术,可以克隆C.elegans基因组的每个基因。优选克隆最小长度为500bp的外显子。如果外显子太小,则用PCR分离较小的片段,或甚至用PCR技术分离多个内含子的部分和相邻的外显子,使得至少克隆足够部分的所述基因的翻译区。为此,需要进行至少17000个PCR反应。将这种PCR产物的收集物克隆在所述T7载体(两个T7启动子彼此相对地定向,在其之间具有一个多克隆位点)中。独立地克隆每种PCR产物,或可以用全部PCR产物产生类似于所述cDNA文库的随机文库。如果单独克隆每种PCR产物,则可以以不同方式汇集所产生的细菌和质粒DNA。首先,可以如在随机文库中所述,将这种分别在T7RNAi载体中克隆的PCR产物的收集物随机地汇集。也可以以更合理的方式进行这种汇集。例如,可以采用生物信息工具(载于silico biology)分析C.elegans基因组的基因。该基因组的不同基因将属于一个基因家族,或在该基因组中具有同源物。汇集该基因家族的这些成员,或将为同源物的成员汇集。以这种方式,将约17000个克隆的总数降至更合用的量。在按照本发明的方法中可以用该文库筛选表型。所产生的表型给出了对C.elegans基因组的所述基因或基因家族或基因同源物的功能描述。由于该文库由该基因组中每个基因的一部分构成,因此该方法使得能够用功能-表型术语描述整个基因组。为此,需要将双链RNA(dsRNA)引入到所述蠕虫中。可以以所述的几种方式,完成这种单独的克隆、或者随机汇集或合理汇集的汇集克隆的引入。
用于表达双链RNAi的载体的实例
可以使用含有T7启动子的任何载体,且所述载体含有一个多克隆位点(有许多市售的载体)。设计具有合适末端的含有T7启动子的引物和具有合适末端的反向互补链的引物。可以将这些引物杂交,并且如果很好地设计,可以将其克隆在选择的载体中。作为T7启动子的最小序列为TAATACGACTCACTATAGGGCGA。尽管可以使用任何载体构建一个T7表达载体,但以下是用载体pGEM-3zf(-)如何完成这一过程的实例。
-用HindⅢ和SalⅠ消化载体pGEM-3zf(+)(PROMEGA)。
-将引物oGN1和oGN2以1μg/30μl的终浓度混合在一起,将其煮沸并缓慢冷却至室温。
-采用标准连接程序将所述引物连接到该载体中。所产生的载体为pGN1(示于图1),它含有彼此相对地定向的两个T7启动子,两个启动子之间含有一个多克隆位点。
oGN1和oGN2的序列为:-oGN1:AGC TGT AAT ACG ACT CAC TAT AGG GCG AGA AGC TT-oGN2:TCG AAA GCT TCT CGC ATA ATA GTG AGT CGT ATT AC
文库构建实施例
从对RNAi敏感的每种生物中分离RNA。一般接着将分离的RNA拷贝为双链cDNA,随后在合适的载体中制备用于克隆。存在几种方法,分子生物学试剂盒可以购自不同公司,包括promega,clontech,boehringer Mannheim、BRL等,所述试剂盒使得能够:
-分离RNA,
-最终可以分离polyA RNA(可利用几种技术和试剂盒)
-用AMV逆转录酶、随机六聚引物和/或寡聚(dT)引物合成第一条链
-用RNA酶H、DNA聚合酶Ⅰ合成第二条链,
-用T4DNA聚合酶填平末端
-用T4DNA连接酶加入一个连接物
-最后用T4多核苷酸激酶处理
-将所述cDNA克隆到所述载体中。
所产生的连接混合物可以被认为是cDNA文库。连接翻译物含有连接到目的载体中的所有该步骤的cDNA。为了安排文库,需要将该连接反应物转化到大肠杆菌菌株中。
       该大肠杆菌文库或DNA文库的应用
产生T7 RNA的菌株:
-一种标准的菌株为BL21(DE3):F-ompT[lon]hsds(r-m-);和大肠杆菌B菌株)λ(DE3)。最后可使用BL21(DE3)的变异体,尽管使用BL21(DE3)pLysS。
-需要构建可以利用的、产生T7RNA聚合酶的任何其它大肠杆菌菌株。可以用市售的噬菌体容易地产生这种菌株,在这种情况下,使用λCE6载体(由Promega提供)。可以用该噬菌体转染几乎每种大肠杆菌,并将产生T7RNA聚合酶。
-RNA酶Ⅲ突变大肠杆菌:
原则上可利用各种菌株,我们选择在第一个实验中使用菌株AB301-105:ma-19,suc-11,bio-3,gdhA2,his95,mc-105,relA1,spoT1,metB1。(kinder等,1973 Mol.Gen.Genet 126:53),但其它菌株可能更适合。用λDE6感染该菌株,由此构建生产T7的变异体。
可以在细菌库(bacteria pool)上培养野生型C.elegans蠕虫。所述细菌正在表达T7RNA聚合酶。这在C.elegans肠中产生大量的dsRNA,dsRNA将在这种生物中扩散,并导致抑制表达。现在可以用该文库筛选几种表型。这种技术的优点是:与已知的C.elegans技术相比,它探测某些途径中的相关基因要快得多。此外,如果发现一种感兴趣的表型,则可以容易地克隆负责的基因。
采用等级汇集,人们可以容易地在第二次筛选中发现该库的相关克隆。然后可以对该克隆的插入DNA进行测序。该实验以一个步骤产生遗传和生化的数据。
可以将野生型C.elegans株系与化合物混合,以根据表型、药物抗性和或药物敏感性进行筛选。所述C.elegans株系可以是突变型株系,根据增强的表型、减弱的表型或新表型筛选。所述C.elegans株系可以是一种突变株系,并且可以将所述文库的筛选与化合物相结合。因此,人们可以筛选药物抗性、药物敏感性、增强的表型、减弱的表型或新表型。所述大肠杆菌菌株可以是表达T7RNA聚合酶的任何菌株,例如像BL21(DE3),但通过采用RNA酶Ⅲ阴性的特殊大肠杆菌菌株,可以增强双链RNA的形成。最后,可以使用非RNA酶Ⅲ的RNA酶缺失的大肠杆菌,或可以使用一种或多种RNA酶缺失的大肠杆菌。T7RNA聚合酶在大多数已知的大肠杆菌菌株和可用来产生生产T7 RNA聚合酶的大肠杆菌菌株的构成物中的表达,一般包括一个诱导型启动子。以这种方式,调节T7RNA聚合酶的产生,并由此产生所述dsRNA。最好是,可以用这一特征来“脉冲式”饲喂特定生长阶段的C.elegans蠕虫。让所述蠕虫生长在非诱导的大肠杆菌菌株上。当所述蠕虫长到目的阶段时,在所述细菌中诱导产生T7RNA。这使得可以在所述动物生活周期中的任何点研究任一基因的功能。筛选文库中推定的目的人类基因的同源物并将功能确定至这些基因
已经在各种计划(为基因组计划、差异表达排列、杂交研究等)中分离出数百个基因。所描述的cDNA文库可以提供一种以快速有效的方式验证功能和或将功能确定至这些基因的方法。首先,需要通过生物信息工具(载于silico biology)鉴定出该蠕虫的一种或多种同源物或所述基因。研制出PCR引物,并用PCR技术分离所述cDNA片段。可以在等级库上进行PCR。将含带有合适cDNA的细菌的阳性库或阳性孔的所述细菌饲喂C.elegans并记录表型。
可以在从C.elegans中分离的cDNA上进行PCR。可将产生的DNA克隆到T7载体中,并转化到所述生产dsRNA的大肠杆菌中,然后用该大肠杆菌饲喂C.elegans蠕虫。需要根据哪种方式更快和更可靠而作出选择。
如果该基因属于一个基因家族,则可能需要用细菌混合物饲喂所述蠕虫。细菌混合物中的每种细菌均含有该基因家族成员的一部分。可以如上所述使用大肠杆菌菌株、生长条件及进行与化合物的混合。
如果使用其中以组织和结构方式克隆C.elegans的所有基因的该文库的合理形式,则可以用silico biology容易地在该文库中追踪回该基因家族的C.elegans同源物,并最终追踪回该基因家族的其它同源物、orthologues和成员。在该步骤中不涉及PCR,可以分离用于养所述蠕虫的细菌和或DNA。
实施例
所述系列实验的:既测试所述RNAi载体和也测试构建的各种大肠杆菌菌株。
1)试验质粒的构建
可以使用当被失效或用于RNAi实验中时在蠕虫中产生清楚表型的任何cDNA。已知unc-22是一个良好的候选者,但可能其它基因也是可以的。我们选择可以用于较晚阶段的一个敏感型系统。用在pha-1背景中的sup-35测试该系统。通过PCR分离sup-35的外显子5,并将其克隆到T7启动子载体pGN1中。产生的载体被命名为pGN2。pha-1(e2123)突变型蠕虫不能在高于25℃的温度下产生后代。这是由于胚胎发生中的发育问题而引起的。当在该株系中sup-35被失效或抑制时,后代可以在该温度下生长。pha-1突变型蠕虫和sup-35RNAi的组合是一个验证各种可选择之物的良好系统。
2)用产生dsRNA的大肠杆菌菌株测试所述RNAi
-将pGN2引入大肠杆菌菌株BL21(DE3)中,并用IPTG诱导T7RNA聚合酶。在该细菌上接种C.elegans蠕虫(pha-1(e2123)),让其在25℃限制温度下生长。因为该突变体在该温度下是胚胎突变体,所以将观察不到后代。如果大肠杆菌中存在的sup-35dsRNA有效抑制sup-35基因,则将观察到后代。
-将pGN2引入大肠杆菌AB301-105(DE3)中,并用IPTG诱导T7RNA聚合酶。在该细菌上接种C.elegans蠕虫(pha-1(e2123)),让其在25℃限制温度下生长。因为该突变体在该温度下是胚胎突变体,所以观察不到后代。如果大肠杆菌中存在的sup-35 dsRNA有效抑制sup-35基因,则将观察到后代。
3)改良蠕虫株系以更好地摄入dsRNA
在将pha-1C.elegans接种到产生双链sup-35RNA的大肠杆菌菌株平板上之前,用EMS(甲磺酸乙酯)诱变该蠕虫。然后将诱变蠕虫的后代接种到所述细菌平板上。摄食该细菌的蠕虫产生较大的后代,所述后代具有导致dsRNA摄入改善的突变,可以将其用于进一步的实验。
所述产生dsRNA的载体稳定地整合到产生T7RNA聚合酶的蠕虫的基因组中
构建具有以下特征的大肠杆菌载体:彼此相对的两个T7启动子,在所述两个启动子之间具有一个限制位点或一个多克隆位点。此外,该载体可以含有C.elegans sup-35基因组DNA,对该载体的工程改造方式使得其在不同的间隔含有几个终止密码子,以致从sup35基因组DNA片段不可能表达出全长蛋白,如图8所示。在所述两个T7启动子之间的多克隆位点中可以克隆任何cDNA或cDNA片段。如果将该载体引入到表达T7RNA聚合酶的C.elegans株系中,则在所述两个T7启动子之间克隆的cDNA或cDNA片段将转录,并从所克隆的片段产生dsRNA。
设计该载体以用于表达T7RNA聚合酶的pha-1(e2123)突变型蠕虫中。T7RNA聚合酶的表达可以是组成型的,或可以被调节,可以是普遍性的或是组织特异性的。这些pha-1(e2123)蠕虫在高于25℃的温度下不能产生后代,这是由于胚胎发生中的发育问题引起的。当在该株系中sup-35被失效或抑制时,后代可以在该温度下生长。
如果将该载体引入到所述蠕虫中,则该载体可以通过同源重组而整合(Campbell样整合)。已经表明,在C.elegans中发生同源重组,尽管其频率低(Plasterk和Groenen,EMBO J.11:287-290,1992)。与sup-35基因的同源重组将导致该基因的失效,因为所产生的两个sup-35基因将含有终止密码子。如果这种重组发生在卵中,则所产生的蠕虫及其后代将具有一个拷贝的整合到基因组中的所述载体。可以将其选择出来,因为仅有sup-35已经被失效的蠕虫在高于25℃的温度下具有后代。此外,所产生的蠕虫将稳定地从所述两个T7启动子之间的克隆的DNA片段产生双链RNA。这种蠕虫现在可以被认为是基因功能减低的稳定的转基因蠕虫株系,而所述基因是所述两个T7启动子之间所克隆片段所属的基因。
可以通过几种技术将所述DNA传递至蠕虫,所述技术包括注射、弹道转化(ballistic transformation)、浸泡在所述DNA溶液中、饲喂所述细菌。可以考虑提高转化率的新方法和其它方法。
另外,C.elegans靶株系可以具有除pha-1(e2123)突变以外的其它突变,并且可以表达除T7 RNA聚合酶以外的其它基因。
实施例B:酵母双杂种-RNAi载体
可以构建含有所述两个T7启动子的酵母双杂种载体。所述载体可被设计为既在酵母中复制,又在大肠杆菌中复制。一般而言,可以在Gal4或LexA载体中制备适合于所述酵母双杂种系统的cDNA文库。在具有这些基因中的一个基因的激活域的载体中构建该文库。可以构建一种载体,该载体在酵母双杂种筛选中仍可以执行功能,但它也含有两个彼此相对定向的T7启动子,并且在所述两个启动子之间具有一个克隆位点。在该质粒中所述序列的顺序则将为“质粒骨架、(GAL4-T7)、MCS、T7、骨架”。在实验中在该载体中构建的C.elegans cDNA文库可以用作标准酵母双杂种文库,以分离与给定蛋白相互作用的蛋白。一旦分离出克隆,则可以将该质粒引入到表达T7RNA聚合酶的大肠杆菌菌株中,并因此将产生所克隆片段的dsRNA。可以将产生该dsRNA的细菌饲喂所述蠕虫,并可记录表型。如先前的实施例中,这种对于新分离的酵母双杂种克隆的验证方法明显比标准方法省时,标准方法需要PCR步骤和/或克隆步骤、RNA实验和/或失效实验。在大多数情况下,首先对分离出的克隆测序,在该序列的基础上,作出继续进行进一步的实验的决定。在本发明中,可以容易地将每个分离出的克隆引入到合适的大肠杆菌中并将其饲喂所述蠕虫。然后通过表型分析进行验证。
为了应用该方法,用一个已知基因作饵,用新构建的文库作为靶,使用酵母双杂种。在所述靶中,由所述克隆编码的与饵蛋白相互作用的蛋白,将产生表达报道分子的阳性酵母克隆,所述报道分子诸如可以通过用X-gal的LacZ染色观察到的报道分子。直接从该酵母菌株中分离出编码靶蛋白的质粒,并将其引入到大肠杆菌中。该大肠杆菌为产生T7RNA聚合酶的大肠杆菌。在这种情况下,从克隆在该载体的多克隆位点中的DNA产生双链RNA。如果用前述方法将该dsRNA饲喂所述蠕虫,则所述基因在蠕虫中被抑制,产生特定表型。
-这种酵母双杂种载体可以有利地用来构建一个先前实施例中所述的有序且等级汇集的文库。
-也可以构建一种有条件地产生T7RNA聚合酶的酵母菌株。在酵母双杂种实验后,可以诱导所述T7聚合酶的表达,导致在酵母细胞中产生dsRNA。因此,可以将该酵母饲喂蠕虫。可得到的证明表明,C.elegans蠕虫可以摄食酵母。
产生T7 RNA聚合酶的菌株的构建及其应用
可以构建表达T7 RNA聚合酶的C.elegans株系。表达可以是普遍的和组成型的,但也可以在一个组织特异性启动子、诱导型启动子或瞬时启动子或含有这些特征之一或特征组合的启动子之下而被调节。可以将DNA引入到该C.elegans株系中。这种引入或者通过注射、用粒子射击、电穿孔进行,或者如上所述通过摄食进行。如果所述DNA为前述实施例中描述的质粒,即在两个侧翼T7启动子之间具有所克隆cDNA片段或PCR片段的质粒,则在所述细胞或整个生物中形成该cDNA或PCR片段的dsRNA,导致向下调节相应的基因。所引入的DNA可以具有有效的瞬时向下调节作用。所引入的DNA可以形成染色体外布置(array),所述布置可能导致更具催化性的功能表型的剔除或降低。该质粒也可能整合到所述生物的基因组中,导致同样催化性的功能表型的剔除或降低,但这可被稳定地传递。
-如实施例A)和B)中所述,可以通过标准技术,将在两个T7启动子之间具有一个克隆的C.elegans cDNA或cDNA部分或EST或PCR片段的质粒引入到T7RNA聚合酶蠕虫中。可以分析表型-可以通过标准技术(注射、射击),将如同实施例A)中的、得自有序汇集文库的DNA引入到T7RNA聚合酶蠕虫中。可以分离表型。用所述等级库,可以容易地发现原始克隆。
-可以用表达T7RNA聚合酶的突变蠕虫完成同样的步骤。筛选增强的、降低的或新的表型。
-可以使用能够筛选化合物的方法。或者用野生型株系或者用突变株系筛选增强的表型或新表型。
-可以用新方法将所述DNA引入到蠕虫中。其中一个方法是用大肠杆菌传递DNA。在这种情况下,用所述等级汇集文库饲喂所述动物。为了防止所述大肠杆菌DNA在线虫肠中被消化,优先使用DNA酶缺陷型C.elegans,例如nuc-1(e1392)。这种方法将的最令人感兴趣的方法,因为它与其它技术的转化效率无关,并且一般更快且工作量更少。
2)该方法推定的增强作用
-设计一种载体,使其含有sup-35cDNA或该cDNA的一部分,将其克隆在两个T7启动子之间。该载体的其余部分如实施例A)和B)中所述。可以将该载体引入到pha-lts突变C.elegans中。在这种情况下存在一个温度选择系统,只有已经摄入所述DNA并表达双链sup-35RNA的那些蠕虫将在限制温度下存活。可以通过上述任何方法传递所述等级汇集文库。
-可以用该载体构建一个文库,将所述载体引入到表达T7 RNA聚合酶的大肠杆菌中。在这种情况下,我们已经如部分A)中所述,类似地进行了筛选,并在sup-35的dsRNA有活性的场合下,对蠕虫进行额外的筛选。
-可以在不同质粒上传递sup-35的DNA和或dsRNA。对于饲喂,即对于DNA饲喂(实施例C)和dsRNA饲喂实施例A)和B),这意味着所述两种质粒可以存在于一种细菌中,或意味着用细菌混合物饲喂蠕虫,其中一种细菌含有sup-35构成物。
构建产生T7 RNA的C.elegans的实施例
为了在所述蠕虫中产生T7RNA聚合酶,有几种可能性。所述T7聚合酶可以在不同启动子下表达,即在诱导型启动子、组成型启动子、普遍性启动子和组织(细胞)特异性启动子或它们的组合下表达。这些启动子的实例是热激启动子hsp-6、肠启动子ges1、得自cet858的启动子,而且也有dpy7的启动子和启动子元件GATA1。在该实施例中,在pPD49.78载体中可利用的hsp-16启动子控制下表达所述T7RNA聚合酶。用GN3和GN4引物,分离作为PCR产物的T7RNA聚合酶。
用NheⅠ和NcoⅠ消化所产生的PCR产物,同样消化我们想用于克隆的载体,即Fire载体pPD49.78。所产生的载体为图2中说明的pGN100,包括oGN3:CAT GGC AGG ATG AAC ACG ATT AAC ATCGC oGN4:ATG GCC CCA TGG TTA CGG GAA CGC GAA GTC CGpGN100。
用标准技术例如微注射,将该载体引入到蠕虫中。
然后构建以下株系:
-野生型(pGN100)
-nuc-1(e1392)(pGN100)
-pha-1(e2123)(pGN100)
-pha-1;nuc-1(pGN100)
当温度诱导时,或者用金属诸如应用重金属镉或汞时,所有这些株系均能够产生T7RNA聚合酶。温度诱导方法是将动物转移至30-33℃的温度下达至少1小时,然后可将所述动物转移回到标准温度(15-25℃)下。
可以用产生T7RNA聚合酶的野生型株系在所述蠕虫中产生任何RNA。更具体地讲,可以将得自所述文库的质粒引入到这些蠕虫中,并可记录表型。
用nuc-1突变蠕虫,通过喂给蠕虫的细菌来引入DNA。因为nuc-1蠕虫不消化所述DNA,所以所述质粒DNA可以穿过肠壁。如果所述DNA被产生T7RNA聚合酶的细胞吸收,则将产生dsRNA,由此抑制转录出所述RNA的基因。
产生T7RNA聚合酶的pha-1突变株系可以用来增强上述方法。可以通过射击、微注射或摄食引入DNA。更具体地讲,对于从sup-35和从目的基因产生dsRNA的载体,可以使用该株系,所述目的基因可以是PCR产物、cDNA或所述的文库。
产生T7RNA聚合酶的pha-1、nuc-1突变体可以用于所述DNA的细菌传递。DNA将优选为从sup-35和目的基因产生dsRNA的质粒。该蠕虫株系将优先在肠中产生T7RNA聚合酶。优选通过用带有该质粒的细菌饲喂蠕虫而发生传递。
RNAi技术在植物中的应用
线虫是使植物受到损害的一个很大原因,对于农业产业中使用的植物更尤其如此。可以将按照本发明的RNAi方法用于植物,以阻止这些寄生线虫摄食更长时间。第一步,从寄生于植物的线虫中分离出对于所述动物生存或生长或摄食或增殖重要的cDNA片段。必需表达的任何基因均适用于此目的。
克隆该基因、外显子或cDNA的一部分。可以将该DNA片段克隆置于组织特异性启动子的影响之下,所述启动子优选根特异性启动子,甚至更优选将该DNA片段克隆在两个根特异性启动子之间。可以用植物转基因技术,将在根特异性启动子控制下的所克隆基因的DNA引入目的植物中。对于每种寄生线虫,可能需要不同片段的DNA,同样,对于每个植物品种,将需要不同的启动子。
当利用根特异性启动子时,根将从引入的DNA片段产生RNA或dsRNA。因为线虫在植物上摄食,故所述线虫将消耗或摄入所述RNA和/或dsRNA。所述RNA和/或dsRNA可以进入线虫的细胞,并对所述靶DNA发挥其抑制作用。根据所克隆的蠕虫的DNA片段的性质,所述线虫将不能存活、进食、增殖等,在所有情况下均阻止该动物在所述植物上更长久地摄食,并因此保护植物。
产生T7RNA聚合酶的C.elegans的构建
为了在动物中、更具体地讲在线虫中,更尤其在C.elegans中产生T7RNA聚合酶或其它RNA聚合酶,可以设想几种可能性。可以在各种启动子下表达T7RNA聚合酶。这些启动子可以是诱导型启动子、组成型启动子、普遍性启动子、组织特异性启动子或它们的组合。
实施例1:
构建用于在C.elegans中表达T7聚合酶的基本载体
用引物oGN26(ATGGAATTCTTACGCGAACGCGAAGTCCG)和oGN46(CTCACCGGTAATGAACACGATTAACATCGC),采用标准方法(PCR,A practical A practical approach,1993,J.McPherson等编辑,IRL Press),从λCE6(Novagen,Madison,USA)经PCR扩增T7聚合酶的编码序列。用AgeⅠ和EcoRⅠ消化所得的编码T7RNA聚合酶的DNA片段,并插入用AgeⅠ和EcoRⅠ消化的Fire载体pPD97.82中。所得的构成物编码一个与SV40大T抗原核定位信号(NLS)融合的T7RNA聚合酶的可读框,其中NLS的氨基酸序列为MTAPKKKRKVPV。将T7RNA聚合酶从胞质转运至细胞核需要这种核定位信号序列,在细胞核中T7RNA聚合酶能够结合于名为T7启动子的其特异性启动子上。T7聚合酶融合蛋白编码序列的上游为最小启动子(myo-2),在最小启动子之前为一个多克隆位点(MCS),在其中可以插入几个C.elegans启动子。该质粒(示于图11的pGN105)为基本T7RNA聚合酶质粒,该质粒能够在C.elegans中表达T7聚合酶。其中将启动子克隆到该质粒多克隆位点中的该质粒衍生物,在C.elegans中可提供T7RNA聚合酶的诱导型、组成型、普遍型和组织特异性表达,因为表达将受到在多克隆位点中所克隆的启动子的调节。
尽管不限于这些实施例,但对于以下启动子,已知它们在以下组织中诱导表达:let-858(遍在表达)、myo-2(咽表达)、myo-3(体壁肌)、egl-15(阴户肌)、unc-119(全身神经元)。
实施例2:
构建用于在C.elegans肌肉组织中表达T7RNA聚合酶的载体
用引物oGN43(GCCACCGGTGCGAGCTCATGAACACGATTAACATCGC)和oGN44(CACTAGTGGGCCCTTACGCGAACGCGAAGTCCG),从λCE6经PCR扩增T7RNA聚合酶的编码序列,用AgeⅠ/SpeⅠ消化,并插入用AgeⅠ/SpeⅠ消化的pGK13载体中。(该载体含有在咽、阴户肌、尾部和体壁肌中驱动表达的强SERCA启动子)。通过将两个重叠寡核苷酸oGN45(CCGGATGACTGCTCCAAAGAAGAAGCGTAAGCT)和oGN46(CTCACCGGTAATGAACACGATTAACATCGC)插入SacⅠ/AgeⅠ限制位点中,将SV40大T抗原的核定位信号(NLS)插入T7聚合酶编码序列之前。将所得的构成物称为pGN108,如图10所示。将该质粒引入到C.elegans中,导致T7 RNA聚合酶在咽、阴户肌、尾部和体壁肌中表达。
为了测试T7 RNA聚合酶在C.elegans中处于SERCA启动子调节下的表达和功能性,将编码在SERCA启动子控制下的T7RNA聚合酶的pGN108注射到C.elegans中。共同注射一种试验载体。该试验载体编码在T7启动子控制下的GFP(图13中的pGN401)。通过将两个重叠的寡核苷酸oGN41(CCCGGGATTAATACGACTCACTATA)和oGN42(CCGGTATAGTGAGTCGTATTAATCCCGGGAGCT)插入SacⅠ/AgeⅠ打开的Fire载体pPD97.82中,产生一个T7启动子,来构建质粒pGN401。此外,共注射一种选择标记以选择转化体(rol6,pRF4)。后一选择载体pRF4是本领域技术人员众所周知的。可以容易地分离出转基因F1,因为它们表现出rol6表型。这些转基因C.elegans均在咽、阴户肌、尾部和体壁肌中表达GFP。该数据清楚地表明,T7RNA聚合酶在SERCA启动子调节下进行功能性表达,并且所表达的T7RNA聚合酶结合于pGN401中存在的T7启动子,从而启动GFP基因的转录,然后功能性地表达GFP,在SERCA正在诱导表达T7RNA聚合酶的肌肉组织中产生荧光。
实施例3:
构建用于在C.elegans中遍在表达T7聚合酶的载体
用XmaⅠ/Bsp1201从pGN108中分离NLS-T7 RNA聚合酶融合基因,将其克隆到用XmaⅠ/Bsp120Ⅰ消化的Fire载体pPD103.05中。这产生一种载体,其中将T7RNA聚合酶克隆在let858启动子调节之下。这种特异性启动子使得能够在所有组织中表达T7RNA聚合酶。将所得的质粒命名为pGN110(图14)。
实施例4:
构建一种载体,用于经T7RNA聚合酶介导在T7启动子控制下表达DNA片段、基因和cDNA
用SacⅠ/AgeⅠ消化Fire载体pPD97.82,通过将两个重叠寡核苷酸oGN41(CCCGGGATTAATACGACTCACTATA)和oGN41(CCGGTATAGTGAGTCGTATTAATCCCGGGAGCT)插入SacⅠ/AgeⅠ限制性内切核酸酶位点中,产生一个T7启动子序列。该构成物(图12中的pGN400)含有一个克隆在SacⅠ和EcoRⅠ限制性内切核酸酶位点之间的、在T7启动子调节之下的GFP可读框。通过缺失作为AgeⅠ/SacⅠ片段的GFP基因,并将目的DNA片段插入该载体中,可以在该载体中克隆任何基因、cDNA或DNA片段。优选可以通过PCR扩增获得目的DNA片段,将其插入引物的SacⅠ/AfeⅠ位点中。将PCR扩增后所得的DNA片段消化,用扩增的DNA片段取代pGN400中的GFP基因。对于在C.elegans中由T7RNA聚合酶诱导的表达而言,可以使用含有T7启动子的每种载体,所述载体诸如市售的pGEM载体和pBluescript载体。通过pGN401载体清楚地表明了这一点:pGN401在表达T7RNA聚合酶的转基因C.elegans中,在T7启动子调节下表达GFP。
应用pGN400的优点是:该载体包括得自unc-54的3’UTR片段,该片段增强所述RNA的转录或稳定性。
永久性、组织特异性“假失效”RNAi C.elegans系的产生
目前,在随机大规模诱变和PCR碱基同胞选择后,获得C.elegans中的基因失效。该方法工作量大、非常耗时并且烦琐。已经描述了,将双链RNA引入到细胞中导致内源基因表达的有效而特异性的干扰。在C.elegans中,通过将RNA注射到该蠕虫的体腔中、将蠕虫浸泡在含dsRNA的溶液中,或饲喂表达对应于目的基因的dsRNA的大肠杆菌,可以向下调节基因的表达。C.elegans细胞具有从其胞外环境中摄入dsRNA的能力。已经报道:mRNA是该ds RNA介导的遗传干扰的靶(Montgomery和Fire1998)。也提示了,在可以发生翻译之前,所述靶RNA在细胞核中被降解。虽然RNAi介导的基因表达的降低可以传递至下一代,但可遗传性差,在更远的后代期间该效应迅速丧失。这可能是由于dsRNA库的持续减少。我们在这里提出一种方法,来构建具有永久性的、可遗传的RNAi表型的C.elegans系。该方法包括:通过将含有义方向和反义方向靶基因cDNA片段的质粒引入并置于蠕虫启动子的控制之下,或通过从单一构成物转录反向重复的所述cDNA,产生转基因C.elegans系。或者,可以在表达T7聚合酶的C.elegans株系中,从含有邻接两个T7启动子的cDNA的载体转录dsRNA。结果是具有可遗传的稳定的“假失效”表型的转基因蠕虫。所述cDNA或T7聚合酶的表达可以是普遍型的和组成型的,但也可以在组织特异性启动子下而被调节。与通过外来ds RNAi(注射的、浸泡的或饲喂的)诱导的RNAi对比,该方法使人们能够获得基因表达的有条件的、组织特异性抑制。
通过RNA干扰抑制unc-22表达导致“痉挛(twicthing)”表型
将unc 22 cDNA(外显子22)以有义和反义方向克隆到pPD103.05中。(A Fire nr L2865)含有能够在所有组织中表达RNA序列的let858启动子。将所得的质粒命名为pGN205(图19a)和pGN207(图19b)。将这些构成物与一种选择标记(rol-6;GFP)一起引入到C.elegans中。转基因F1个体(表达rol-6或GFP)表现出“痉挛”表型,表明RNAi可以通过从转基因DNA内源转录的RNA来介导。RNAi表型与所述选择标记共分离到更远的后代。这导致具有永久性RNAi表型的C.elegans系的产生。
稳定系T7RNA聚合酶系的产生和双转基因蠕虫的产生
在C.elegans中基于外源RNA聚合酶的一种表达系统要求两种质粒。一种质粒编码在特异性启动子控制之下的RNA聚合酶,而另一种质粒编码在T7启动子调节下表达的DNA片段。对于也称为假稳定失效的半稳定RNAi而言,将目的DNA克隆到两个T7启动子之间,使得可以产生dsRNA。
因为已知T7RNA聚合酶表达系统是一种高效表达系统,所以这将导致产生双转基因动物的问题。如果要在C.elegans线虫中表达的基因有毒性,则这将导致致死效应,并因此导致在构建出的C.elegans中没有目的基因的高度调节的稳定表达。如果目的基因对于所述生物的生存是必不可少的,则具有得自该基因的DNA片段的RNAi也将导致致死效应,使得不可能假稳定失效。
为了解决这一问题,本发明人已经设计出一种由两种转基因动物组成的系统。第一种动物为T7RNA聚合酶的转基因动物,正如前述实施例中所表明的,这种T7RNA聚合酶可以在所有细胞或特定细胞或组织中表达。第二种转基因动物是目的DNA片段的转基因动物。这可以是连接于T7启动子的基因或cDNA,或者如果人们想要进行RNAi,则它可以是克隆在两个T7启动子之间的这样的基因的DNA片段。
这两种转基因动物均是活的,并且不表现出任何异常表型。这是因为在第一种转基因生物中表达的T7RNA聚合酶即使以相对高水平表达,也对该生物无毒性。在第二种转基因生物中,不表达目的基因,或者不产生所述dsRNA,因为这些转基因动物不含有T7RNA聚合酶。
通过让这两种转基因动物交配,可以获得目的基因或目的cDNA的表达、或具有DNA片段的RNAi。这些转基因动物的后代是双转基因动物,并且表达目的基因,或表达目的DNA片段的dsRNA。为了在这种交配中产生足够的雄性动物,其中一种所述转基因雄性动物可以是具有适于产生雄性的表型的C.elegans突变体。这样一种突变体的实例是him-5。将优选用这样一种突变体来产生T7RNA聚合酶的转基因C.elegans,而雌雄同体动物含有在T7启动子调节下的所述DNA片段。
为了有效选择所述双转基因后代,可以将一种第二转基因引入到所述第二种转基因动物中。这种转基因含有一个在T7启动子调节下的报道基因。所述报道基因可以是GFP、荧光素酶、β半乳糖苷酶或β-内酰胺酶。这种转基因的实例是载体pGB400和pGN401。
为了在C.elegans中获得转基因的可诱导的组织特异性表达,我们可以产生这样的雄性原种(即him-5):所述雄性原种(即him-5)携带使得能够进行例如组织特异性表达的不同C.elegans启动子控制下的T7聚合酶构成物。可以使这种雄性动物与携带在T7启动子控制下的目的基因的雌雄同体交杂。
此外,可以将所述转基因整合到动物的基因组中。已经描述了导致质粒稳定地整合到动物基因组中的方法(Methods in cell biology,第48卷,1995,epstein和Shakes编辑,Academic Press),所述方法涉及对所述动物辐照。可以对两种动物辐照,但优选对表达T7RNA聚合酶的动物进行这种处理。这产生一群在不同启动子控制下稳定表达T7RNA聚合酶的C.elegans线虫,这样的启动子的实例是myo-2(咽表达)、myo-3(体壁肌)、dgl-15(阴户肌)、unc-119(全身神经元)、SERCA(肌肉)、let858(所有细胞)、ges-1(肠)。
RNAi T7启动子酵母双杂种载体的构建
具有正向和反向T7T3和或Sp6的pGAD424
在大多数双杂种实验中,用已经进行工程改造的、在多接头中具有额外限制位点(诸如Ncol位点)的质粒pGAD424(图16)(Clontech),克隆一个cDNA文库。该文库便于在酵母双杂种实验中筛选结合蛋白。我们构建了一种新的酵母双杂种载体,该载体具有完成酵母双杂种的同样的可能性,但它含有两个额外的T7启动子,使得该载体可以用于T7RNA聚合酶诱导的假稳定失效。为此,通过用一个T7接头(由以下引物aattcttaatacgactcactatagggcc和catgggccctatagtgagtcgtattaag构成),我们将一个正向T7插入pGAD424的EcoRⅠ-NcoⅠ位点中。我们将所得的载体命名为pGAD424-without-FULL-ICE-both-T7。小心地去除终止密码子并使用最大多接头可匹配的氨基酸。对于反向T7(由两种引物gatccgtcgacagatctccctatagtgagtcgtattactgca和gtaatacgactcactatagggagatctgtcgacg构成),我们采用同一策略并使用BamH1和Pat1。为了避免丧失SalⅠ,我们在所述引物中包括了这一位点。
所述SalⅠ位点是重要的,因为大多数文库均在该位点克隆,连接物也买得到。这使得新构建的载体与现有的载体相容。
具有正向和反向T7/T3和或Sp6的pAS2
基于pAS2(Clontech)构建了一种类似的酵母双杂种载体。通过用EcoRⅤ部分消化,我们能够去除cyh2基因相当大的部分。可以分离出正确的构成物,并通过用BglⅡ限制消化进行检查,该位点存在于被去除的PAS2的EcoRⅤ片段中。这消除了略有毒性并涉及生长延迟的cyh2基因。该基因对于进行RNAi和酵母双杂种实验不是必不可少的。在消除EcoR片段后,位于编码GAL4DB和HA(表位)的DNA序列之间的EcoRⅠ限制位点成为该载体唯一的EcoRⅠ限制位点,可以用来用含接头的T7启动子取代HA。这确保所有的限制位点存留,允许既符合读框地克隆,也与先前的载体和pAD424相容。我们使用了以下接头(引物:aattcttaatacgactcactatagggca和tatgccctatagtgagtcgtattaag),使用EcoRⅠ和NdeⅠ克隆位点。我们采用同一策略用于反向T7(引物:gatccgtcgacagatctccctatagtgagtcgtattactgcacatgggccctatagtgagtcgtattaag和gtaatacgactcactatagggagatctgtcgacg),使用BamH1和Pst1。为了避免丧失Sal1,我们在所述引物中包括了该位点。将所得的载体命名为pAS2-cyh2-HA+both T7-final。
在PGAD424中具有T7启动子(或者T3,或SP6启动子),使得可以很快地从相互作用蛋白转变至RNAi,并将功能确定至所分离的DNA片段。另一优点是具有这样一种能力,即能够通过与体外翻译偶联的体外转录(有一个ATG或者GAL4DB或者GAL4AD的读框符合),制备可以用于体外控制(例如摧毁(pull down)测定)实际蛋白-蛋白相互作用的标记蛋白。
在以下提供的序列表中确定了所产生的质粒序列和SP6和T3聚合酶的序列。SP6 DNA依赖性RNA聚合酶:SEQENCEID NO.1swissprot登录号P06221蛋白序列:1 mqdlhaiqlq leeemfnggi rrfeadqgrq iaagsesdta wnrrllseli apmaegiqay61 keeyegkkgr apralaflqc venevaayit mkvvmdmlnt datlqaiams vaeriedqvr121 fskleghaak yfekvkkslk asrtksyrha hnvavvaeks vaekdadfdr weawpketql181 gigttlleil egsvfyngep vfmramrtyg gktiyylqts esvgqwisaf kehvaglspa241 yapcvipprp wrtpfnggfh tekvasrirl vkgnrehvrk ltqkqmpkvy kainalqntq301 wqinkdvlav ieevirldlg ygvpsfkpli dkenkpanpv pvefqhlrgr elkemlsgeq361 wqqfinwkge carlytaetk rgsksaavvr mvgqarkysa fesiyfvyam dsrsrvyvqs421 stlspqsndl gkallrfteg rpvngvealk wfcinganlw gwdkktfdvr vsnvldeefq481 dmcrdiaadp ltftqwakad apyeflawcf eyaqyldlvd egradefrth lpvhqdgscs541 giqhysamlr devgakavnl kpsdapqdiy gavaqvvikk nalymdadda ttftsgsvtl601 sgtelramas awdsigitrs ltkkpvmtlp ygstrltcre svidyivdle ekeaqkavae661 grtankvhpf eddrgdyltp gaaynymtal iwpsisevvk apivamkmir qlarfaakrn721 eglmytlptg fileqkimat emlrvrtclm gdikmslqve tdivdeaamm gaaapnfvhg781 hdashliltv celvdkgvts iavihdsfgt hadntltlrv alkgqmvamy idgnalqkll841 eehevrwmvd tgievpegge fdlneimdse yvfaT3DNA依赖性RNA聚合酶:SEQENCEIDNO.2swissprot登录号P07659蛋白序列:1 mniieniekn dfseielaai pfntladhyg salakeqlal ehesyelger rflkmlerqa61 kageiadnaa akpllatllp klttrivewl eeyaskkgrk psayaplqll kpeasafitl121 kvilasltst nmttiqaaag mlgkaiedea rfgrirdlea khfkkhveeq lnkrhgqvyk181 kafmqvvead migrgllgge awsswdkett mhvgirliem liestglvel qrhnagnags241 dhealqlaqe yvdvlakrag alagispmfq pcvvppkpwv aitgggywan grrplalvrt301 hskkglmrye dvympevyka vnlaqntawk inkkvlavvn eivnwkncpv adipslerqe361 lppkpddidt neaalkewkk aaagiyrldk arvsrrisle fmleqankfa skkaiwfpyn421 mdwrgrvyav pmfnpqgndm tkglltlakg kpigeegfyw lkihgancag vdkvpfperi481 afiekhvddi lacakdpinn twwaeqdspf cflafcfeya gvthhglsyn cslplafdgs541 csgiqhfsam lrdevggrav nllpsetvqd lygivaqkvn eilkqdaing tpnemitvtd601 kdtgeisekl klgtstlaqq wlaygvtrsv tkrsvmtlay gskefgfrqq vlddtiqpai661 dsgkglmftq pnqaagymak liwdavsvtv vaaveamnwl ksaakllaae vkdkktkeil721 rhrcavhwtt pdgfpvwqey rkplqkrldm iflgqfrlqp tintlkdsgi dahkqesgia781 pnfvhsqdgs hlrmtvvyah ekygiesfal ihdsfgtipa dagklfkavr etmvityenn841 dvladfysqf adqlhetqld kmpplpkkgn lnlqdilksd fafapGN10g:                                        SEQUENCE ID NO. 3gttgtcgtaaagagatgtttttattttactttacaccgggtcctctctctctgccagcacagctcagtgttggctgtgtgctcgggctcctgccaccggcggcctcatcttcttcttcttcttctctcctgctctcgcttatcacttcttcattcattcttattccttttcatcatcaaactagcatttcttactttatttatttttttcaattttcaattttcagataaaaccaaactacttgggttacagccgtcaacagatccccgggattggccaaaggacccaaaggtatgtttcgaatgatactaacataacatagaacattttcaggaggacccttgcttggagggtaccggatgactgctccaaagaagaagcgtaagctcatgaacacgattacatcgctaagaacgacttctctgacatcgaactggctgctatcccgttcaacactctggctgaccattacggtgagcgtttagctcgcgaacagttggcccttgagcatgagtcttacgagatgggtgaagcacgcttccgcaagatgtttgagcgtcaacttaaagctggtgaggttgcggataacgctgccgccaagcctctcatcactaccctactccctaagatgattgcacgcatcaacgactggtttgaggaagtgaaagctaagcgcggcaagcgcccgacagccttccagttcctgcaagaaatcaagccggaagccgtagcgtacatcaccattaagaccactctggcttgcctaaccagtgctgacaatacaaccgttcaggctgtagcaagcgcaatcggtcgggccattgaggacgaggctcgcttcggtcgtatccgtgaccttgaagctaagcactrcaagaaaaacgttgaggaacaactcaacaagcgcgtagggcacgtctacaagaaagcatttatgcaagttgtcgaggctgacatgctctctaagggtctactcggtggcgaggcgtggtcttcgtggcataaggaagactctattcatgtaggagtacgctgcatcgagatgctcattgagtcaaccggaatggttagcttacaccgccaaaatgctggcgtagtaggtcaagactctgagactatcgaactcgcacctgaatacgctgaggctatcgcaacccgtgcaggtgcgctggctggcatctctccgatgttccaaccttgcgtagttcctcctaagccgtggactggcattactggtggtggctattgggctaacggtcgtcgtcctctggcgctggtgcgtactcacagtaagaaagcactgatgcgctacgaagacgtttacatgcctgaggtgtacaaagcgattaacattgcgcaaaacaccgcatggaaaatcaacaagaaagtcctagcggtcgccaacgtaatcaccaagtggaagcattgtccggtcgaggacatccctgcgattgagcgtgaagaactcccgatgaaaccggaagacatcgacatgaatcctgaggctctcaccgcgtggaaacgtgctgccgctgctgtgtaccgcaagacaaggctcgcaagtctcgccgtatcagccttgagttcatgcttgagcaagccaataagtttgctaaccataaggccatctggttcccttacaacatggactggcgcggttcgtgtttacgctgtgtcaatgttcaacccgcaaggtaacgatatgaccaaaggacgtcttacgctggcgaaaggtaaaccaatcggtaaggaaggttactactggctgaaaatccacggtgcaaactgtgcgggtgtcgataaggtttcgtttcctgagcgcatcaagttcattgaggaaaaccacgagaacatcatggcttgcgctaagtctccactggagaaacacttggtgggctgagcaagattctccgttctgcttccttgcgttctgctttgagtacgctggggtacagcaccacggcctgagctataactgctcccttccgctggcgtttgacgggtcttgctctggcatccagcacttctccgcgatgctccgagatgaggtaggtggtcgcgcggttaacttgcttcctagtgaaaccgttcaggacatctacgggattgttgctaagaaagtcaacgagattctgcaagcagacgcaatcaatgggaccgataacgaagtagttacctgtgaccgatgagaacactggtgaaatctctgagaaagtcaagctgggcactaaggcactggctggtcaatggctggcttacggtgttactcgcagtgtgactaagcgttcagtcatgacgctggcttacgggtccaaagagttcggcttccgtcaacaagtgctggaagataccattcagccagctattgattccggcaagggtctgatgttcactcagccgaatcaggctgctggatacatggctaagctgatttgggaatccgtgagcgtgacggtggtagctgcggttgaagcaatgaactggcttaagtctgctgctaagctgctggctgctgaggtcaaagataagaagactggagagattcttcgcaagcgttgcgctgtgcattgggtaactcctgatggtttccctgtgtggcaggaatacaagaagcctattcagacgcgcttgaacctgatgttcctcggtcagttccgcttacagcctaccattaacaccaacaaagatagcgagattgatgcacacaaacaggagtctggtatcgctcctaactttgtacacagccaagacggtagccaccttcgtaagactgtagtgtgggcacacgagaagtacggaatcgaatcttttgcactgattcacgactccttcggtaccattccggctgacgctgcgaacctgttcaaagcagtgcgcgaaactatggttgacacatatgagtcttgtgatgtactggctgatttctacgaccag ttcgctgaccagttgcacgagtctcaattggacaaaatgccagcacttccggctaaaggtaacttgaacctccgtgacatcttagagtcggacttcgcgttcgcgtaagggcccactagtcggccgtacgggccctttcgtctcgcgcgtttcggtgatgacggtgaaaacctctgacacatgcagctcccggagacggtcacagcttgtctgtaagcggatgccgggagcagacaagcccgtcagggcgcgtcagcgggtgtttggcgggtgtcggggctggcttaactatgcggcatcagagcagattgtactgagagtgcaccatatgcggtgtgaaataccgcacagatgcgtaaggagaaaataccgcatcaggcggccttaagggcctcgtgatacgcctatttttataggttaatgtcatgataataatggtttcttagacgtcaggtggcacttttcggggssatgtgcgcggaacccctatttgtttatttttctaaatacattcaaatatgtatccgctcatgagacaataaccctgataaatgcttcaataatattgaaaaaggaagagtatgaatattcaacatttccgtgtcgcccttattcccttttttgcggcattttgccttcctgtttttgctcacccagaaacgctggtgaaagtaaaagatgctgaagatcagttgggtgcacgagtgggttacatcgaactggatctcaacagcggtaagatccttgagagttttcgccccgaagaacgttttccaatgatgagcacttttaaagttctgctatgtggcgcggtattatcccgtattgacgccgggcaagagcaactcggtcgccgcatacactattctcagaatgacttggttgagtactcaccagtcacagaaaagcatcttacggatggcatgacagtaagagaattatgcagtgctgccataaccatgagtgataacactgcggccaacttacttctgacaacgatcggaggaccgaaggagctaaccgcttttttgcacaacatgggggatcatgtaactcgccttgatcgttgggaaccggagctgaatgaagccataccaaacgacgagcgtgacaccacgatgcctgtagcaatggcaacaacgttgcgcaaactattaactggcgaactacttactctagcttcccggcaacaattaatagactggatggaggcggataaagttgcaggaccacttctgcgctcggcccttccggctggctggtttattgctgataaatctggagccggtgagcgtgggtctcgcggtatcattgcagcactggggccagatggtaagccctcccgtatcgtagttatctacacgacggggagtcaggcaactatggatgaacgaaatagacagatcgctgagataggtgcctcactgattaagcattggtaactgtcagaccaagtttactcatatatactttagattgatttaaaacttcatttttaatttaaaaggatctaggtgaagatcctttttgataatctcatgaccaaaatcccttaacgtgagttttcgttccactgagcgtcagaccccgtagaaaagatcaaaggatcttcttgagatcctttttttctgcgcgtaatctgctgcttgcaaacaaaaaaaccaccgctaccagcggtggtttgtttgccggatcaagagctaccaactctttttccgaaggtaactggcttcagcagagcgcagataccaaatactgtccttctagtgtagccgtagttaggccaccacttcaagaactctgtagcaccgcctacatacctcgctctgctaatcctgttaccagtggctgctgccagtggcgataagtcgtgtcttaccgggttggactcaagacgatagttaccggataaggcgcagcggtcgggctgaacggggggttcgtgcacacagcccagcttggagcgaacgacctacaccgaactgagatacctacagcgtgagcattgagaaagcgccacgcttcccgaagggagaaaggcggacaggtatccggtaagcggcagggtcggaacaggagagcgcacgagggagcttccagggggaaacgcctggtatctttatagtcctgtcgggtttcgccacctctgacttgagcgtcgttttttgtgatgctcgtcaggggggcggagcctatggaaaaacgccagcaacgcggcctttttacggttcctggccttttgctggccttttgctcacatgttcttccctgcgttatcccctgattctgtggataaccgtattaccgcctttgagtgagctgataccgctcgccgcagccgaacgaccgagcgcagcgagtcagtgagcgaggaagcggaagagcgcccaatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcggtgcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttcacacaggaaacagctatgaccatgattacgccaagctgtaagtttaaacatgatcttactaactaactattctcatttaaattttcagagcttaaaaatggctgaaatcactcacaacgatggatacgctaacaacttggaaatgaaataagcttgcatgcctgcagagcaaaaaaatactgcttttccttgcaaaattcggtgctttcttcaaagagaaacttttgaagtcggcgcgagcatttccttctttgacttctctctttccgccaaaaagcctagcatttttattgataatttgattacacacactcagagttcttcgacatgataaagtgtttcattggcactcgccctaacagtacatgacaagggcggattattatcgatcgatattgaagacaaactccaaatgtgtgctcattttggagccccgtgtggggcagctgctctcaatatattactagggagacgaggagggggaccttatcgaacgtcgctgagccattctttcttctttatgcactctcttcactctctcacacattaatcgattcatagactcccatattcctrgatgaaggtgtgggtttttagctttttttcccgatttgtaaaaggaagaggctgacgatgttaggaaaaagagaacggagccgaaaaaacatccgtagtaagtcttccttttaagccgacactttttagacagcattcgccgctagttttgaagtttaaattttaaaaaataaaaattagtttcaattttttttaattactaaataggcaaaagttttttcaagaactctagaaaaactagcttaattcatgggtactagaaaaattcttgttttaaatttaatatttatcttaagatgtaattaccgagaagcttttttgaaaattctcaattaaaagaatttgccgatttagaataaaagtcttcagaaatgagtaaaagctcaaattagaagtttgtttttaaaggaaaaacacgaaaaaagaacactatttatcttttcctccccgcgtaaaattagttgttgtgataatagtgatccgctgtctatttgcactcggctcttcacaccgtgcttcctctcacttgacccaacaggaaaaaaaaacatcacgtctgagacggtgaattgccttatcaagagcgtcgtctctttcacccagtaacaaaaaaaatttggtttctttactttatatttatgtaggtcacaaaaaaaaagtgatgcagttttgtgggtcggttgtctccacaccacctccgcctccagcagcacacaatcatcttcgtgtgttctcgacgattccttgtatgccgcggtcgtgaatgcaccacattcgacgcgcaactacacaccacactcactttcggtggtattactacacgtcatcgttgttcgtagtctcccgctctttcgtccccactcactcctcattattccccttggtgtattgattttttttaaatggtacaccactcctgacgtttctaccttcttgttttccgtccatttagattttatctggaaatttttttaaaattttaggccagagagttctagttcttgttctaaaagtctaggtcagacatacattttctatttctcatcaaaaaaaaagttgataaagaaaactggttattcagaaagagtgtgtctcgttgaaattgattcaaaaaaaaattcccacccctcgcttgtttctcaaaatatgagatcaacggattttttccttctcgattcaattttttgctgcgctctgtctgccaaagtgtgtgtgtccgagcaaaagatgagagaatttacaaacagaaatgaaaaaaagttggccaaataatgaagttttatccgagattgatgggaaagatattaatgttctttacggtttggaggggagagagagatagattttcgcatcaaactccgccttttacatgtcttttagaatctaaaatagatttttctcatcatttttaatagaaaatcgagaaattacagtaatttcgcaattttcttgccaaaaatacacgaaatttgtgggtctcgccacgatctcggtcttagtggttcatttggtttaaaagtttataaaatttcaaattctagtgtttaatttccgcataattggacctaaaatgggtttttgtcatcattttcaacaagaaatcgtgaaaatcctgttgtttcgcaattttcttttcaaaaaacacgaaatatatggtaatttcccgaaatattgagggtctcgccacgatttcagtcacagtggccaggatttatcacgaaaaaagttcgcctagtctcacatttccggaaaaccgaatctaaattagttttttgtcatcattttgaacaaaaaatcgagacatccctatagtttcgcaattttcgtcgcttttctctccaaaaatgacagtctagaattaaaattcgctggaactgggaccatgatatcttttctccccgtttttcatttttattttttattacactggattgactaaaggtcaccaccaccgccagtgtgtgccatatcacacacacacacacacacaatgtcgagattttatgtgttatccctgcttgatttcgttccgttgtctctctctctctattcatcttttgagccgagaagctccagagaatggagcacacaggatcccggcgcgcgatgtcgtcgggagatggcgccgcctgggaagccgccgagagatatcagggaagatcgtctgatttctcctcggatgccacctcatctctcgagtttctccgcctgttactccctgccgaacctgatatttcccpGN105:                                   SEQUENCE ID NO.4aagcttgcatgcctgcaggccttggtcgactctagacacttttcagctacctagatacatggatatccccgcctcccaatccacccacccagggaaaaagaagggctcgccgaaaaatcaaagttatctccaggctcgcgcatcccaccgagcggttgacttctctccaccacttttcattttaaccctcggggtacgggattggccaaaggacccaaaggtatgtttcgaatgatactaacataacatagaacattttcaggaggacccttgcttggagggtaccgagctcagaaaaaatgactgctccaaagaagaagcgtaaggtaccggtaatgaacacgattaacatcgctaagaacgacttctctgacatcgaactggctgctatcccgttcaacactctggctgaccattacggtgagcgtttagctcgcgaacagttggcccttgagcatgagtcttacgagatgggtgaagcacgcttccgcaagatgtttgagcgtcaacttaaagctggtgaggttgcggataacgctgccgccaagcctctcatcactaccctactccctaagatgattgcacgcatcaacgactggtttgaggaagtgaaagctaagcgcggcaagcgcccgacagccttccagttcctgcaagaaatcaagccggaagccgtagcgtacatcaccattaagaccactctggcttgcctaaccagtgctgacaatacaaccgttcaggctgtagcaagcgcaatcggtcgggccattgaggacgaggctcgcttcggtcgtatccgtgaccttgaagctaagcacttcaagaaaaacgttgaggaacaactcaacaagcgcgtagggcacgtctacaagaaagcatttatgcaagttgtcgaggctgacatgctctctaagggtctactcggtggcgaggcgtggtcttcgtggcataaggaagactctattcatgtaggagtacgctgcatcgagatgctcattgagtcaaccggaatggttagcttacaccgccaaaatgctggcgtagtaggtcaagactctgagactaatcgaactcgcacctgaatacgctgaggctatcgcaacccgtgcaggtgcgctggctggcatctctccgatgttccaaccttgcgtagttcctcctaagccgtggactggcattactggtggtggctattgggctaacggtcgtcgtcctctggcgctggtgcgtactcacagtaagaaagcactgatgcgctacgaagacgtttacatgcctgaggtgtacaaagcgattaacattgcgcaaaacaccgcatggaaaatcaacaagaaagtcctagcggtcgccaacgtaatcaccaagtggaagcattgtccggtcgaggacatccctgcgattgagcgtgaagaactcccgatgaaaccggaagacatcgacatgaatcctgaggctctcaccgcgtggaaacgtgctgccgctgctgtgtaccgcaaggacagggctcgcaagtctcgccgtatcagccttgagttcatgcttgagcaagccaataagtttgctaaccataaggccatctggttcccttacaacatggactggcgcggtcgtgtttacgccgtgtcaatgttcaacccgcaaggtaacgatatgaccaaaggactgcttacgctggcgaaaggtaaaccaatcggtaaggaaggttactactggctgaaaatccacggtgcaaactgtgcgggtgtcgataaggttccgttccctgagcgcatcaagttcattgaggaaaaccacgagaacatcatggcttgcgctaagtctccactggagaacacttggtgggctgagcaagattctccgttctgcttccttgcgttctgctttgagtacgctggggtacagcaccacggcctgagctataactgctcccttccgctggcgtttgacgggtcttgctctggcatccagcacttctccgcgatgctccgagatgaggtaggtggtcgcgcggttaacttgcttcctagtgagaccgttcaggacatctacgggattgttgctaagaaagtcaacgagattctacaagcagacgcaatcaatgggaccgataacgaagtagttaccgtgaccgatgagaacactggtgaaatctctgagaaagtcaagctgggcactaaggcactggctggtcaatggctggctcacggtgttactcgcagtgtgactaagcgttcagtcatgacgctggcttacgggtccaaagagttcggcttccgtcaacaagtgctggaagataccattcagccagctattgattccggcaagggtccgatgttcactcagccgaatcaggctgctggatacatggctaagctgatttgggaatctgtgagcgtgacggtggtagctgcggttgaagcaatgaactggcttaagtctgctgctaagctgctggctgctgaggtcaaagataagaagactggagagattcttcgcaagcgttgcgctgtgcattgggtaactcctgatggtttccctgtgtggcaggaatacaagaagcctattcagacgcgcttgaacctgatgttcctcggtcagttccgcttacagcctaccattaacaccaacaaagatagcgagattgatgcacacaaacaggagtctggtatcgctcctaactttgtacacagccaagacggtagccaccttcgtaagactgtagtgtgggcacacgagaagtacggaatcgaatcttttgcactgattcacgactccttcggtaccattccggctgacgctgcgaacctgttcaaagcagtgcgcgaaactatggttgacacatatgagtcttgtgatgtactggctgatttctacgaccagttcgctgaccagttgcacgagtctcaattggacaaaatgccagcacttccggctaaaggtaacttgaacctccgtgacatcttagagtcggacttcgcgttcgcgtaagaattccaactgagcgccggtcgctaccattaccaacttgtctggtgtcaaaaataataggggccgctgtcatcagagtaagtttaaactgagttctactaactaacgagtaatatttaaattttcagcatctcgcgcccgtgcctctgacttctaagtccaattactcttcaacatccctacatgctctttctccctgtgctcccaccccctatttttgttattatcaaaaaaacttcttcttaatttctttgttttttagcttcttttaagtcacctctaacaatgaaattgtgtagattcaaaaatagaattaattcgtaataaaaagtcgaaaaaaattgtgctccctccccccattaataataattctatcccaaaatctacacaatgttctgtgtacacttcttatgttttttttacttctgataaattttttttgaaacatcatagaaaaaaccgcacacaaaataccttatcatatgttacgtttcagtttatgaccgcaatttttatttcttcgcacgtctgggcctctcatgacgtcaaatcatgctcatcgtgaaaaagttttggagtatttttggaatttttcaatcaagtgaaagtttatgaaattaattttcctgcttttgctttttgggggtttcccctattgtttgtcaagagtttcgaggacggcgtttttcttgctaaaatcacaagtattgatgagcacgatgcaagaaagatcggaagaaggtttgggtttgaggctcagtggaaggtgagtagaagttgataatttgaaagtggagtagtgtctatggggtttttgccttaaatgacagaatacattcccaatataccaaacataactgtttcctactagtcggccgtacgggccctttcgtctcgcgcgtttcggtgatgacggtgaaaacctctgacacatgcagctcccggagacggtcacagcttgtctgtaagcggatgccgggagcagacaagcccgtcagggcgcgtcagcgggtgttggcgggtgtcggggctggcttaactatgcggcatcagagcagattgtactgagagtgcaccatatgcggtgtgaaataccgcacagatgcgtaaggagaaaataccgcatcaggcggccttaagggcctcgtgatacgcctatttttataggttaatgtcatgataataatggtttcttagacgtcaggtggcacttttcggggaaatgtgcgcggaacccctatttgtttatttttcttaatacattcaaatatgtatccgctcatgagacaataaccctgataaatgcttcaataatattgaaaaaggaagagtatgagtattcaacacttccgtgtcgcccttattcccctttttgcggcattttgccttcccgtttttgctcacccagaaacgctggtgaaagtaaaagatgctgaagatcagttgggtgcacgagtgggttacatcgaactggatctcaacagcggtaagatccttgagagttttcgccccgaagaacgttttccaatgatgagcacttttaaagttctgctatgtggcgcggtattatcccgtattgacgccgggcaagagcaactcggtcgccgcatacactattctcagaatgacttggttgagtactcaccagtcacagaaaagcatcttacggatggcatgacagtaagagaattatgcagtgctgccataaccatgagtgataacactgcggccaacttacttctgacaacgatcggaggaccgaaggagctaaccgctttcttgcacaacatgggggatcatgtaactcgccttgatcgttgggaaccggagctgaatgaagccataccaaacgacgagcgtgacaccacgatgcctgtagcaatggcaacaacgttgcgcaaactattaactggcgaactacttactccagcttcccggcaacaattaatagactggatggaggcggataaagttgcaggaccacttctgcgctcggcccttccggctggctggtttattgctgataaatctggagccggtgagcgtgggtctcgcggcatcattgcagcactggggccagacggtaagccctcccgtatcgtagttatccacacgacggggagtcaggcaactatggatgaacgaaatagacagatcgctgagataggtgcctcactgattaagcattggtaactgtcagaccaagtttactcatatatactttagattgatttaaaacttcatttttaatttaaaaggatctaggtgaagatcctttttgataatctcatgaccaaaatcccttaacgtgagttttcgttccactgagcgtcagaccccgtagaaaagatcaaaggatcttcttgagatcctttttttctgcgcgtaatctgctgcttgcaaacaaaaaaaccaccgctaccagcggtggtttgtttgccggatcaagagctaccaactcttttccgaaggtaactggcttcagcagagcgcagataccaaatactgtccttctagtgtagccgtagttaggccaccacttcaagaactctgtagcaccgcctacatacctcgctctgctaatcctgttaccagtggctgctgccaatggcgataaatcgtgtcttaccgggttggactcaagacgatagttaccggataaggcgcagcggtcgggctgaacggggggttcgtgcacacagcccagcttggagcgaacgacctacaccgaactgagatacctacagcgtgagcattgagaaagcgccacgcttcccgaagggagaaaggcggacaggtatccggtaagcggcagggtcggaacaggagagcgcacgagggagcttccagggggaaacgcctggtatctttatagtcctgtcgggtttcgccacctctgacttgagcgtcgatttttgtgatgctcgtcaggggggcggagcctatggaaaaacgccagcaacgcggcctttttacggttcctggccttttgctggccttttgctcacatgttctttcctgcgttatcccctgattctgtggataaccgtattaccgcctttgagtgagctgataccgctcgccgcagccgaacgaccgagcgcagcgagtcagtgagcgaggaagcggaagagcgcccaatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttcacacaggaaacagctatgaccatgattacgccaagctgtaagtttaaacatgatcttactaactaactattctcatttaaattttcagagcttaaaaatggctgaaatcactcacaacgatggatacgctaacaacttggaaagaaatpGN400:                                          SEQUENCE ID NO.5aagcttgcatgcctgcaggccttggtcgactctagacacttttcagctacctagatacatggatatccccgcctcccaatccacccacccagggaaaaagaagggctcgccgaaaaatcaaagttatctccaggctcgcgcatcccaccgagcggttgacttctctccaccacttttcattttaaccctcggggtacgggattggccaaaggacccaaaggtatgtttcgaatgatactaacataacatagaacattttcaggaggacccttgcttggagggtaccgagctcccgggattaatacgactcactataccggtagaaaaaatgagtaaaggagaagaacttttcactggagttgtcccaattcttgttgaattagatggtgatgttaatgggcacaaattttctgtcagtggagagggtgaaggtgatgcaacatacggaaaacttacccttaaatttatttgcactactggaaaactacctgttccatgggtaagtttaaacatatatatactaactaaccctgattatttaaattttcagccaacacttgtcactactttctgttatggtgttcaatgcttctcgagatacccagatcatatgaaacggcatgactttttcaagagtgccatgcccgaaggttatgtacaggaaagaactatatttttcaaagatgacgggaactacaagacacgtaagtttaaacagttcggtactaactaaccatacatatttaaattttcaggtgctgaagtcaagtttgaaggtgatacccttgttaatagaatcgagttaaaaggtattgattttaaagaagatggaaacattcttggacacaaattggaatacaactataactcacacaatgtatacatcatggcagacaaacaaaagaatggaatcaaagttgtaagtttaaacatgattttactaactaactaatctgatttaaattttcagaacttcaaaattagacacaacattgaagatggaagcgttcaactagcagaccattatcaacaaaatactccaattggcgatggccctgtccttttaccagacaaccattacctgtccacacaatctgccctttcgaaagatcccaacgaaaagagagaccacatggtccttcttgagtttgtaacagctgctgggattacacatggcatggatgaactatacaaatagcattcgtagaattccaactgagcgccggtcgctaccattaccaacttgtctggtgtcaaaaataataggggccgctgtcatcagagtaagtttaaactgagttctactaactaacgagtaatatttaaattttcagcatctcgcgcccgtgcctctgacttctaagtccaattactcttcaacatccctacatgctctttctccctgtgctcccaccccctatttttgttattatcaaaaaaacttcttcttaatttctttgttttttagcttcttttaagtcacctctaacaatgaaattgtgtagattcaaaaatagaattaattcgtaataaaaagtcgaaaaaaattgtgctccctccccccattaataataattctatcccaaaatctacacaatgttctgtgtacacttcttatgttttttttacttctgataaattttttttgaaacatcatagaaaaaaccgcacacaaaataccttatcatatgttacgtttcagtttatgaccgcaatttttatttcttcgcacgtctgggcctctcatgacgtcaaatcatgctcatcgtgaaaaagttttggagtatttttggaatttttcaatcaagtgaaagttatgaaattaattttcctgcttttgctttttgggggtttcccctattgtttgtcaagagtttcgaggacggcgtttttcttgctaaaatcacaagtattgatgagcacgatgcaagaaagatcggaagaaggtttgggtttgaggctcagtggaaggtgagtagaagttgataatttgaaagtggagtagtgtctatggggtttttgccttaaatgacagaatacattcccaatataccaaacataactgtttcctactagtcggccgtacgggccctttcgtctcgcgcgtttcggtgatgacggtgaaaacctctgacacatgcagctcccggagacggtcacagcttgtctgtaagcggatgccgggagcagacaagcccgtcagggcgcgtcagcgggtgttggcgggtgtcggggctggcttaactatgcggcatcagagcagattgtactgagagtgcaccatatgcggtgtgaaataccgcacagatgcgtaaggagaaaataccgcatcaggcggccttaagggcctcgtgatacgcctatttttataggttaatgtcatgataataatggtttcttagacgtcaggtggcacttttcggggaaatgtgcgcggaacccctatttgtttatttttctaaatacattcaaatatgtatccgctcatgagacaataaccctgataaatgcttcaataatattgaaaaaggaagagtatgagtattcaacatttccgtgtcgcccttattcccttttttgcggcattttgccttcctgtttttgctcacccagaaacgctggtgaaagtaaaagatgctgaagatcagttgggtgcacgagtgggttacatcgaactggatctcaacagcggtaagatccttgagagttttcgccccgaagaacgttttccaatgatgagcacttttaaagttctgctatgtggcgcggtattatcccgtattgacgccgggcaagagcaactcggtcgccgcatacactattctcagaatgacttggttgagtactcaccagtcacagaaaagcatcttacggatggcatgacagtaagagaattatgcagtgctgccataaccatgagtgataacactgcggccaacttacttctgacaacgatcggaggaccgaaggagctaaccgcttttttgcacaacatgggggatcatgtaactcgccttgatcgttgggaaccggagctgaatgaagccataccaaacgacgagcgtgacaccacgatgcctgtagcaatggcaacaacgttgcgcaaactattaactggcgaactacttactctagcttcccggcaacaattaatagactggatggaggcggataaagttgcaggaccacttctgcgctcggcccttccggctggctggtttattgctgataatctggagccggtgagcgtgggtctcgcggtatcattgcagcactggggccagatggtaagccctcccgtatcgtagttatctacacgacggggagtcaggcaactatggatgaacgaaatagacagatcgctgagataggtgcctcactgattaagcattggtaactgtcagaccaagtttactcatatatactttagattgatttaaaacttcatttttaatttaaaaggatctaggtgaagatcctttttgataatctcatgaccaaaatcccttaacgtgagttttcgttccactgagcgtcagaccccgtagaaaagatcaaaggatcttcttgagatcctttttttctgcgcgtaatctgctgcttgcaaacaaaaaaaccaccgctaccagcggtggtttgtttgccggatcaagagctaccaactctttttccgaaggtaactggcttcagcagagcgcagataccaaatactgtccttctagtgtagccgtagttaggccaccacttcaagaactctgtagcaccgcctacatacctcgctctgctaatcctgttaccagtggctgctgccagtggcgataagtcgtgtcttaccgggttggactcaagacgatagttaccggataaggcgcagcggtcgggctgaacggggggttcgtgcacacagcccagcttggagcgaacgacctacaccgaactgagatacctacagcgtgagcattgagaaagcgccacgcttcccgaagggagaaaggcggacaggtatccggtaagcggcagggtcggaacaggagagcgcacgagggagcttccagggggaaacgcctggtatctttatagtcctgtcgggtttcgccacctctgacttgagcgtcgatttttgtgatgctcgtcaggggggcggagcctatggaaaaacgccagcaacgcggcctttttacggttcctggccttttgctggccttttgctcacatgttctttcctgcgttatcccctgattctgtggataaccgtattaccgcctttgagtgagctgataccgctcgccgcagccgaacgaccgagcgcagcgagtcagtgagcpggaagcggaagagcgcccaatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttcacacaggaaacagctacgaccatgattacgccaagccgtaagtttaaacatgatcttactaactaactattctcatttaaattttcagagcttaaaaacggctgaaatcactcacaacgatggatacgctaacaacttggaaatgaaatpGN401                                             SEQUENCE ID NO.6gatcccggcgcgcgatgtcgttcgggagatggcgccgcctgggaagccgccgagagatatcagggaagatcgtctgatttctcctcggatgccacctcatctctcgagtttctccgcctgttactccctgccgaacctgatatttcccgttgtcgtaaagagatgtttttattttactttacaccgggtcctctctctctgccagcacagctcagtgttggctgtgtgctcgggctcctgccaccggcggcctcatcttcttcttcttcttctctcctgctctcgcttatcacttcttcattcattcttattccttttcatcatcaaactagcatttcttactttatttatttttttcaattttcaattttcagataaaaccaaactacttgggttacagccgtcaacagatccccgggattggccaaaggacccaaaggtatgtttcgaatgatactaacataacatagaacattttcaggaggacccttgcttggagggtaccggtagaaaaaatgagtaaaggagaagaacttttcactggagttgtcccaattcttgttgaattagatggtgatgttaatgggcacaaattttctgtcagtggagagggtgaaggtgatgcaacatacggaaaacttacccttaaatttatttgcactactggaaaactacctgttccatgggtaagtttaaacatatatatactaactaaccctgattatttaaattttcagccaacacttgtcactactttctgttatggtgttcaatgcttctcgagatacccagatcatatgaaacggcatgactttttcaagagtgccatgcccgaaggttatgtacaggaaagaactatatttttcaaagatgacgggaactacaagacacgtaagtttaaacagttcggtactaactaaccatacatatttaaattttcaggtgctgaagtcaagtttgaaggtgatacccttgttaatagaatcgagttaaaaggtattgatttaaagaagatggaaacattcttggacacaaattggaatacaactataactcacacaatgtatacatcatggcagacaaacaaaagaatggaatcaaagttgtaagtttaaacttggacttactaactaacggattatatttaaattttcagaacttcaaaattagacacaacattgaagatggaagcgttcaactagcagaccattatcaacaaaatactccaattggcgatggccctgtccttttaccagacaaccattacctgtccacacaatctgccctttcgaaagatcccaacgaaaagagagaccacatggtccttcttgagtttgtaacagctgctgggattacacatggcatggatgaactatacaaatagcattcgtagaattccaactgagcgccggtcgctaccattaccaacttgtctggtgtcaaaaataataggggccgctgtcatcagagtaagtttaaactgagttctactaactaacgagtaatatttaaattttcagcatctcgcgcccgtgcctctgacttctaagtccaattactcttcaacatccctacatgctctttctccctgtgctcccaccccctatttttgttattatcaaaaaaacttcttcttaatttctttgttttttagcttcttttaagtcacctctaacaatgaaattgtgagattcaaaaatagaattaattcgtaataaaaagtcgaaaaaaattgtgctccctccccccattaataataattctatcccaaaatctacacaatgttctgtgtacacttcttatgttttttttacttctgataaattttttttgaaacatcatagaaaaaaccgcacacaaaataccttatcatatgttacgtttcagtttatgaccgcaatttttatttcttcgcacgtctgggcctctcatgacgtcaaatcatgctcatcgtgaaaaagttttggagtatttttggaatttttcaatcaagtgaaagtttatgaaattaattttcctgcttttgctttttgggggtttcccctattgtttgtcaagagtttcgaggacggcgtttttcttgctaaaatcacaagtattgatgagcacgatgcaagaaagatcggaagaaggtttgggtttgaggctcagtggaaggtgagtagaagttgataatttgaaagtggagtagtgtctatggggtttttgccttaaatgacagaatacattcccaatataccaaacataactgtttcctactagtcggccgtacgggcccggtacccagcttttgttccctttagtgagggttaattgcgcgcttggcgtaatcatggtcatagctgtttcctgtgtgaaattgttatccgctcacaattccacacaacatacgagccggaagcataaagtgtaaagcctggggtgcctaatgagtgagctaactcacattaattgcgttgcgctcactgcccgctttccagtcgggaaacctgtcgtgccagctgcattaatgaatcggccaacgcgcggggagaggcggtttgcgtattgggcgctcttccgcttcctcgctcactgactcgctgcgctcggtcgttcggctgcggcgagcggtatcagctcactcaaaggcggtaatacggttatccacagaatcaggggataacgcaggaaagaacatgtgagcaaaaggccagcaaaaggccaggaaccgtaaaaaggccgcgttgctggcgtttttccataggctccgcccccctgacgagcatcacaaaaatcgacgctcaagtcagaggtggcgaaacccgacaggactataaagataccaggcgtttccccctggaagctccctcgtgcgctctcctgttccgaccctgccgcttaccggatacctgtccgcctttctcccttcgggaagcgtggcgctttctcatagctcacgctgtaggtatctcagttcggtgtaggtcgttcgctccaagctgggctgtgtgcacgaaccccccgttcagcccgaccgctgcgccttatccggtaactatcgtcttgagtccaacccggtaagacacgacttatcgccactggcagcagccactggtaacaggattagcagagcgaggtatgtaggcggtgctacagagttcttgaagtggtggcctaactacggctacactagaaggacagtatttggtatctgcgctctgctgaagccagttaccttcggaaaaagagttggtagctcttgatccggcaaacaaaccaccgctggtagcggtggtttttttgtttgcaagcagcagattacgcgcagaaaaaaaggatctcaagaagatcctttgatcttttctacggggtctgacgctcagtggaacgaaaactcacgttaagggattttggtcatgagattatcaaaaaggatcttcacctagatccttttaaattaaaaatgaagttttaaatcaatctaaagtatatatgagtaaacttggtctgacagttaccaatgcttaatcagtgaggcacctatctcagcgatctgtctatttcgttcatccatagttgcctgactccccgtcgtgtagataactacgatacgggagggcttaccatctggccccagtgctgcaatgataccgcgagacccacgctcaccggctccagatttatcagcaataaaccagccagccggaagggccgagcgcagaagtggtcctgcaactttatccgcctccatccagtctattaattgttgccgggaagctagagtaagtagttcgccagttaatagtttgcgcaacgttgttgccattgcacaggcatcgtggtgtcacgctcgtcgtttggtatggcttcattcagctccggttcccaacgatcaaggcgagttacatgatcccccatgttgtgcaaaaaagcggttagctccttcggtcctccgatcgttgtcagaagtaagttggccgcagtgttatcactcatggttatggcagcactgcataattctcttactgtcatgccatccgtaagatgcttttctgtgactggtgagtactcaaccaagtcattctgagaatagtgtatgcggcgaccgagttgctcttgcccggcgtcaatacgggataataccgcgccacatagcagaactttaaaagtgctcatcattggaaaacgttcttcggggcgaaaactctcaaggatcttaccgctgttgagatccagttcgatgtaacccactcgtgcacccaactgatcttcagcatcttttactttcaccagcgtttctgggtgagcaaaaacaggaaggcaaaatgccgcaaaaaagggaataagggcgacacggaaatgttgaatactcatactcttcctttttcaatattattgaagcatttatcagggttattgtctcatgagcggatacatatttgaatgtatttagaaaaataaacaaataggggttccgcgcacatttccccgaaaagtgccacctaaattgtaagcgttaaattttgttaaaattcgcgttaaatttttgttaaatcagctcattttttaaccaataggccgaaatcggcaaaatcccttataaatcaaaagaatagaccgagatagggttgagtgttgttccagtttggaacaagagtccactattaaagaacgtggactccaacgtcaaagggcgaaaaaccgtctatcagggcgatggcccactacgtgaaccatcaccctaatcaagttttttggggtcgaggtgccgtaaagcactaaatcggaaccctaaagggagcccccgatttagagcttgacggggaaagccggcgaacgtggcgagaaaggaagggaagaaagcgaaaggagcgggcgctagggcgctggcaagtgtagcggtcacgctgcgcgtaaccaccacacccgccgcgcttaatgcgccgctacagggcgcgtcccattcgccattcaggctgcgcaactgttgggaagggcgatcggtgcgggcctcttcgctattacgccagctggcgaaagggggatgtgctgcaaggcgattaagttgggtaacgccagggttttcccagtcacgacgttgtaaaacgacggccagtgagcgcgcgtaatacgactcactatagggcgaattggagctccaccgcggtggcggccgctctagaactagtgpGN110:                                      SEQUENCE ID NO.7gatcctccaaaatcgtcttccgctctgaaaaacgaaagtggacctttgacatccgaaaaaatgggcgaaaaaatgaaattgagctttttgggtcgaaaaaaatgtttttagaatgctgagaacacgttaaacacgaagatcatatttattttgagacccggatgctctgaaaatgtctgacatagatttaaaaaagcatatatatatttttcattttcaacgtgaaagttttgtgcaactttatagaatctcctattggcacattgttttttatttaactgaggcagtttttgaacacctttttgaaactttgaatctctttgaagtatactgtcgaaaagactgacttgagcgttcgaaatgccagaagaaaactatatttgaatctcgcgctaaattgagaaatgcaaccgcgctccactggacaattggaaaaaaaatttattcggaggcgacaacggtattttcgaaattgattttctgtgtattttctcattttttataaattcttctttgatttatcgttcgtttgtgagaaatttaattgtattcaaacttttttatagtaagataccggtggtaccgctagccgtacgaacccgggattggccaaaggacccaaaggtatgtttcgaatgatactaacataacatagaacattttcaggaggacccttgcttggagggtaccggatgactgctccaaagaagaagcgtaagctcatgaacacgattaacatcgctaagaacgacttctctgacatcgaactggctgctatcccgttcaacactctggctgaccattacggtgagcgtttagctcgcgaacagttggcccttgagcatgagtcttacgagatgggtgaagcacgcttccgcaagatgtttgagcgtcaacttaaagctggtgaggttgcggataacgctgccgccaagcctctcatcactaccctactccctaagatgattgcacgcatcaacgactggtttgaggaagtgaaagctaagcgcggcaagcgcccgacagccttccagttcctgcaagaaatcaagccggaagccgtagcgtacatcaccattaagaccactctggcttgcctaaccagtgctgacaatacaaccgttcaggctgtagcaagcgcaatcggtcgggccattgaggacgaggctcgcttcggtcgtatccgtgaccttgaagctaagcacttcaagaaaaacgttgaggaacaactcaacaagcgcgtagg gcacgtctacaagaaagcatttatgcaagttgtcgaggctgacatgctctctaagggtctactcggtggcgaggcgtggtcttcgtggcataaggaagactctattcatgtaggagtacgctgcatcgagatgctcattgagtcaaccggaatggttagcttacaccgccaaaatgctggcgtagtaggtcaagactctgagactatcgaactcgcacctgaatacgctgaggctatcgcaacccgtgcaggtgcgctggctggcatctctccgatgttccaaccttgcgtagttcctcctaagccgtggactggcattactggtggtggctattgggctaacggtcgtcgtcctctggcgctggtgcgtactcacagtaagaaagcactgatgcgctacgaagaacgtttacatgcctgaggtgtacaaagcgattaacattgcgcaaaacaccgcatggaaaatcaacaagaaagtcctagcggtcgccaacgtaatcaccaagtggaagcattgtccggtcgaggacatccctgcgattgagcgtgaagaactcccgatgaaaccggaagacatcgacatgaatcctgaggctctcaccgcgtggaaacgtgctgccgctgctgtgtaccgcaagacaaggctcgcaagtctcgccgtatcagccttgagttcatgcttgagcaagccaataagtttgctaaccataaggccatctggttcccttacaacatggactggcgcggttcgtgtttacgctgtgtcaatgttcaacccgcaaggtaacgatatgaccaaaggacgtcttacgctggcgaaaggtaaaccaatcggtaaggaaggttactactggctgaaaatccacggtgcaaactgtgcgggtgtcgataaggtttcgtttcctgagcgcatcaagttcattgaggaaaaccacgagaacatcatggcttgcgctaagtctccactggagaacacttggtgggctgagcaagattctccgttctgcttccttgcgttctgctttgagtacgctggggtacagcaccacggcctgagctataactgctcccttccgctggcgtttgacgggtcttgctctggcatccagcacttctccgcgatgctccgagatgaggtaggtggtcgcgcggttaacttgcttcctagtgaaaccgttcaggacatctacgggattgttgctaagaaagtcaacgagattctgcaagcagacgcaatcaatgggaccgataacgaagtagttaccgtgaccgatgagaacactggtgaaatctctgagaaagtcaagctgggcactaaggcactggctggtcaatggctggcttacggtgttactcgcagtgtgactaagcgttcagtcatgacgctggcttacgggtccaaagagttcggcttccgtcaacaagtgctggaagataccattcagccagctattgattccggcaagggtctgatgttcactcagccgaatcaggctgctggatacatggctaagctgatttgggaatccgtgagcgtgacggtggtagctgcggttgaagcaatgaactggcttaagtctgctgctaagctgctggctgctgaggtcaaagataagaa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tatccgctcacaattccacacaacatacgagccggaagcataaagtgtaaagcctggggtgcctaatgagtgaggtaactcacattaattgcgttgcgctcactgcccgctttccagtcgggaaacctgtcgtgccagctggattaatgaatcggccaacgcgcggggagaggcggtttgcgtattgggcgctcttccgcttcctcgctcactgactcgctgcgctcggtcgttcggctgcggcgagcggtatcagctcactcaaaggcggtaatacggttatccacagaatcaggggataacgcaggaaagaacatgtgagcaaaaggccagcaaaaggccaggaaccgtaaaaaggccgcgttgctggcgtttttccataggctccgcccccctgacgagcatcacaaaaatcgacgctcaagtcagaggtggcgaaacccgacaggactataaagataccaggcgtttccccctggaagctccctcgtgcgctctcctgttccgaccctgccgcttaccggatacctgtccgcctttctcccttcgggaagcgtggcgctttctcatagctcacgctgtaggtatctcagttcggtgtaggtcgttcgctccaagctgggctgtgtgcacgaaccccccgttcagcccgaccgctgcgccttatccggtaactatcgtcttgagtccaacccggtaagacacgacttatcgccactggcagcagccactggtaacaggattagcagagcgaggtatgtaggcggtgctacagagttcttgaagtggtggcctaactacggctacactagaaggacagtatttggtatctgcgctctgctgaagccagttaccttcggaaaaagagttggtagctcttgatccggcaaacaaaccaccgctggtagcggtggtttttttgtttgcaagcagcagattacgcgcagaaaaaaaggatctcaagaagatcctttgatcttttctacggggtctgacgctcagtggaacgaaaactcacgttaagggattttggtcatgagattatcaaaaaggatcttcacctagatccttttaaattaaaaatgaagttttaaatcaatctaaagtatatatgagtaaacttggtctgacagttaccaatgcttaatcagtgaggcacctatctcagcgatctgtctatttcgttcatccatagttgcctgactccccgtcgtgtagataactacgatacgggagggcttaccatctggccccagtgctgcaatgataccgcgagacccacgctcaccggctccagatttatcagcaataaaccagccagccggaagggccgagcgcagaagtggtcctgcaactttatccgcctccatccagtctattaattgttgccgggaagctagagtaagtagttcgccagttaatagtttgcgcaacgttgttgccattgctacaggcatcgtggtgtcacgctcgtcgtttggtatggcttcattcagctccggttcccaacgatcaaggcgagttacatgatcccccatgttgtgcaaaaaagcggttagctccttcggtcctccgatcgttgtcagaagtaagttggccgcagtgttatcactcatggttatggcagcactgcataatctcttactgtcatgccatccgtaagatgcttttctgtgactggtgagtactcaaccaagtcattctgagaatagtgtatgcggcgaccgagttgctcttgcccggcgtcaatacgggataataccgcgccacatagcagaactttaaaagtgctcatcattggaaaacgttcttcggggcgaaaactctcaaggatcttaccgctgttgagatccagttcgatgtaacccactcgtgcacccaactgatcttcagcatcttttactttcaccagcgtttctgggtgagcaaaaacaggaaggcaaaatgccgcaaaaagggaataagggcgacacggaaatgttgaatactcatactcttcctttttcaatattattgaagcatttatcagggttattgtctcatgagcggatacatatttgaatgtatttagaaaataaacaaataggggttccgcgcacatttccccgaaaagtgccacctgaacgaagcatctgtgcttcattttgtagaacaaaaatgcaacgcgagagcgctaatttttcaaacaaagaatctgagctgcatttttacagaacagaaatgcaacgcgaaagcgctattttaccaacgaagaatctgtgcttcatttttgtaaaacaaaaatgcaacgcgagagcgctaatttttcaaacaaagaatctgagctgcatttttacagaacagaaatgcaacgcgagagcgctattttaccaacaaagaatctatacttcttttttgttctacaaaaatgcatcccgagagcgctatttttctaacaaagcatcttagattactttttttctcctttgtgcgctctataatgcagtctcttgataactttttgcactgtaggtccgttaaggttagaagaaggctactttggtgtcattttctcttccataaaaaaagcctgactccacttcccgcgtttactgattactagcgaagctgcgggtgcattttttcaagataaaggcatccccgattatattctataccgatgtggattgcgcatactttgtgaacagaaagtgatagcgttgatgattcttcattggtcagaaaattatgaacggtttcttctattttgtctctatatactacgtataggaaatgtttacattttcgtattgttttcgattcactctatgaatagttcttactacaatttttttgtctaaagagtaatactagagataaacataaaaaatgtagaggtcgagtttagatgcaagttcaaggagcgaaaggtggatgggtaggttatatagggatatagcacagagatatatagcaaagagatacttttgagcaatgtttgtggaagcggtattcgcaatattttagtagctcgttacagtccggtgcgtttttggttttttgaaagtgcgtcttcagagcgcttttggttttcaaaagcgctctgaagttcctatactttctagagaataggaacttcggaataggaacttcaaagcgtttccgaaaacgagcgcttccgaaaatgcaacgcgagctgcgcacatacagctcactgttcacgtcgcacctatatctgcgtgttgcctgtatatatatatacatgagaagaacggcatagtgcgtgtttatgcttaaatgcgtacttatatgcgtctatttatgtaggatgaaaggtagtctagtacctcctgtgatattatcccattccatgcggggtatcgtatgcttccttcagcactaccctttagctgttctatatgctgccactcctcaattggattagtctcatccttcaatgctatcatttcctttgatattggatcatattaagaaaccattattatcatgacattaacctataaaaataggcgtatcacgaggccctttcgtctcgcgcgtttcggtgatgacggtgaaaacctctgacacatgcagctcccggagacggtcacagcttgtctgtaagcggatgccgggagcagacaagcccgtcagggcgcgtcagcgggtgttggcgggtgtcggggctggcttaactatgcggcatcagagcagattgtactgagagtgcaccatagatcaacgacattactatatatataatataggaagcatttaatagacagcatcgtaatatatgtgtactttgcagttatgacgccagatggcagtagtggaagatattctttattgaaaaatagcttgtcaccttacgtacaatcttgatccggagcttttctttttttgccgattaagaattaattcggtcgaaaaaagaaaaggagagggccaagagggagggcattggtgactattgagcacgtgagtatacgtgattaagcacacaaaggcagcttggagtatgtctgttattaatttcacaggtagttctggtccattggtgaaagtttgcggcttgcagagcacagaggccgcagaatgtgctctagattccgatgctgacttgctgggtattatatgtgtgcccaatagaaagagaacaattgacccggttattgcaaggaaaatttcaagtcttgtaaaagcatataaaaatagttcaggcactccgaaatacttggttggcgtgtttcgtaatcaacctaaggaggatgttttggctctggtcaatgattacggcattgatatcgtccaactgcatggagatgagtcgtggcaagaataccaagagttcctcggtttgccagttattaaaagactcgtatttccaaaagactgcaacatactactcagtgcagcttcacagaaacctcattcgtttattcccttgtttgattcagaagcaggtgggacaggtgaacttttggattggaactcgatttctgactgggttggaaggcaagagagccccgaaagcttacattttatgttagctggtggactgacgccagaaaatgttggtgatgcgcttagattaaatggcgttattggtgttgatgtaagcggaggtgtggagacaaatggtgtaaaagactctaacaaaatagcaaatttcgtcaaaaatgctaagaaataggttattactgagtagtatttatttaagtattgtttgtgcacttgccgatctctgcggtgtgaaataccgcacagatgcgtaaggagaaaataccgcatcaggaaattgtaaacgttaatattttgttaaaattcgcgttaaatttttgttaaatcagctcattttttaaccaataggccgaaatcggcaaaatcccttataaatcaaaagaatagaccgagatagggttgagtgttgttccagtttggaacaagagtccactattaaagaacgtggactccaacgtcaaagggcgaaaaaccgtctatcagggcgatggcccactacgtgaaccatcaccctaatcaagttttttggggtcgaggtgccgtaaagcactaaatcggaaccctaaagggagcccccgatttagagcttgacggggaaagccggcgaacgtggcgagaaaggaagggaagaaagcgaaaggagcgggcgctagggcgctggcaagtgtagcggtcacgctgcgcgtaaccaccacacccgccgcgcttaatgcgccgctacagggcgcgtcgcgccattcgccattcaggctgcgcaactgttgggaagggcgatcggtgcgggcctcttcgctattacgccagctggcgaaagggggatgtgctgcaaggcgattaagttgggtaacgccagggttttcccagtcacgacgttgtaaaacgacggccagtcgtccaagctttcgcgagctcgagatcccgagctttgcaaattaaagccttcgagcgtcccaaaaccttctcaagcaaggttttcagtataatgttacatgcgtacacgcgtctgtacagaaaaaaaagaaaaatttgaaataataaataacgttctttaactaacataactataaaaaaataaatagggacctagacttcaggttgtctaactccttccttttcggttagagcggatgtggggggagggcggtgaatgtaagcgtgacataactaattacatgatatccttttgttgtttccgggtgtacaatatggacttcctcttttctggcaaccaaacccatacatcgggattcctataataccttcgttggtctccctaacatgtaggtggcggaggggagatatacaatagaacagataccagacaagacataatgggctaaacaagactacaccaattacactgcctcattgatggtggtacataacgaactaatactgtaagccctagacttgatagccatcatcatatcgaagtttcactaccctttttccatttgccatctattgaagtaataaataggcgcatgcaacttcttttctttttttttcttttctctctcccccgttgttgtctcaccatatccgcaatgacaaaaaaaatgatggaagacactaaaggaaaaaattaacgacaaagacagcaccaacagatgtcgttgttccagagctgatgaggggtatcttcgaacacacgaaactttttccttccttcattcacgcacactactctctaatgagcaacggtataacggccttccttccagttacttgaatttgaaataaaaaaagtttgccgctttgctatcaagtataaatagacctgcaattattaatcttttgtttcctcgtcattgttctcgttccctttcttccttgtttctttttctgcacaatatttcaagctataccaagcatacaatcaactccaagcttgaagcaagcctcctgaaagatgaagctaactgtcttctatcgaacaagcatgcgatatttgccgacttaaaaagctcaagtgctccaaagaaaaaccgaagtgcgccaagtgtctgaagaacaactgggagtgtcgctactctcccaaaaccaaaaggtctccgctgactagggcacatctgacagaagtggaatcaaggctagaaagactggaacagctatttctactgatttttcctcgagaagaccttgacatgattttgaaaatggattctttacaggatataaaagcattgttaacaggattatttgtacaagataatgtgaataaagatgccgtcacagatagattggcttcagtggagactgatatgcctctaacattgagacagcatagaataagtgcgacatcatcatcggaagagagtagtaacaaaggtcaaagacagttgactgtatcgccggaattcttaatacgactcactatagggcatatggccatggaggccccgggpGGAD424-without-FULL-ICE-BOTH-T7                         SEQUENCE ID NO.9gatccgtcggacggatctccctatagtgagtcgtattactgcagagatctatgaatcgtagatactgaaaaaccccgcaagttcacttcaactgtgcatcgtgcaccatctcaatttctttcatttatacatcgttttgccttcttttatgtaactatactcctctaagtttcaatcttggccatgtaacctctgatctatagaattttttaaatgactagaattaatgcccatcttttttttggacctaaattcttcatgaaaatatattacgagggcttattcagaagctttggacttcttcgccagaggtttggtcaagtctccaatcaaggttgtcggcttgtctaccttgccagaaatttacgaaaagatggaaaagggtcaaatcgttggtagatacgttgttgacacttctaaataagcgaatttcttatgatttatgatttttattattaaataagttataaaaaaaataagtgtatacaaattttaaagtgactcttaggttttaaaacgaaaattcttgttcttgagtaactctttcctgtaggtcaggttgctttctcaggtatagcatgaggtcgctcttattgaccacacctctaccggcatgcccgaaattcccctaccctatgaacatattccattttgtaatttcgtgtcgtttctattatgaatttcatttataaagtttatgtacaaatatcataaaaaaagagaatctttttaagcaaggattttcttaacttcttcggcgacagcatcaccgacttcggtggtactgttggaaccacctaaatcaccagttctgatacctgcatccaaaacctttttaactgcatcttcaatggccttaccttcttcaggcaagttcaatgacaatttcaacatcattgcagcagacaagatagtggcgatagggtcaaccttattctttggcaaatctggagcagaaccgtggcatggttcgtacaaaccaaatgcggtgttcttgtctggcaaagaggccaaggacgcagatggcaacaaacccaaggaacctgggataacggaggcttcatcggagatgatatcaccaaacatgttgctggtgattataataccatttaggtgggttgggttcttaactaggatcatggcggcagaatcaatcaattgatgttgaaccttcaatgtaggaaattcgttcttgatggtttcctccacagtttttctccataatcttgaagaggccaaaacattagctttatccaaggaccaaataggcaatggtggctcatgttgtagggccatgaaagcggccattcttgtgattctttgcacttctggaacggtgtattgttcactatcccaagcgacaccatcaccatcgtcttcctttctcttaccaaagtaaatacctcccactaattctcttgacaacaacgaagtcagtacctttagcaaattgtggcttgattggagataagtctaaaagagagtcggatgcaaagttacatggtcttaagttggcgtacaattgaagttctttacggatttttagtaaaccttgttcaggtctaacactacctgtaccccatttaggaccacccacagcacctaacaaaacggcatcaaccttcttggaggcttccagcgcctcatctggaagtgggacacctgtagcatcgatagcagcaccaccaattaaatgattttcgaaatcgaacttgacattggaacgaacatcagaaatagctttaagaaccttaatggcttcggctgtgatttcttgaccaacgtggtcacctggcaaaacgacgatcttcttaggggcagacattagaatggtatatccttgaaatatatatatattgctgaaatgtaaaaggtaagaaaagttagaaagtaagacgattgctaaccacctattggaaaaaacaataggtccttaaataatattgtcaacttcaagtattgtgatgcaagcatttagtcatgaacgcttctctattccatatgaaaagccggttccggcctctcacctttcctttttctcccaatttttcagttgaaaaaggtatatgcgtcaggcgacctctgaaattaacaaaaaatttccagtcatcgaatttgattctgtgcgatagcgcccctgtgtgttctcgttatgttgaggaaaaaaataatggttgctaagagattcgaactcttgcatcttacgatacctgagtattcccacagttggggatctcgactctagctagaggatcaattcgtaatcatggtcatagctgtttcctgtgtgaaattgttatccgctcacaattccacacaacatacgagccggaagcataaagtgtaaagcctggggtgcctaatgagtgaggtaactcacattaattgcgttgcgctcactgcccgctttccagtcgggaaacctgtcgtgccagctggattaatgatcggccaacgcgcggggagaggcggtttgcgtattgggcgctcttccgcttcctcgctcactgactcgctgcgctcggtcgttcggctgcggcgagcggtatcagctcactcaaaggcggtaatacggttatccacagaatcaggggataacgcaggaaagaacatgtgagcaaaaggccagcaaaaggccaggaaccgtaaaaaggccgcgttgctggcgtttttccataggctccgcccccctgacgagcatcacaaaaatcgacgctcaagtcagaggtggcgaaacccgacaggactataaagataccaggcgtttccccctggaagctccctcgtgcgctctcctgttccgaccctgccgcttaccggatacctgtccgcctttctcccttcgggaagcgtggcgctttctcatagctcacgctgtaggtatctcagttcggtgtaggtcgttcgctccaagctgggctgtgtgcacgaaccccccgttcagcccgaccgctgcgccttatccggtaactatcgtcttgagtccaacccggtaagacacgacttatcgccactggcagcagccactggtaacaggattagcagagcgaggtatgtaggcggtgctacagagttcttgaagtggtggcctaactacggctacactagaaggacagtatttggtatctgcgctctgctgaagccagttaccttcggaaaaagagttggtagctcttgatccggcaaacaaaccaccgctggtagcggtggtttttttgtttgcaagcagcagattacgcgcagaaaaaaaggatctcaagaagatcctttgatcttttctacggggtctgacgctcagtggaacgaaaactcacgttaagggattttggtcatgagattatcaaaaaggatcttcacctagatccttttaaattaaaaatgaagttttaaatcaatctaaagtatatatgagtaaacttggtctgacagttaccaatgcttaatcagtgaggcacctatctcagcgatctgtctatttcgttcatccatagttgcctgactccccgtcgtgtagataactacgatacgggagggcttaccatctggccccagtgctgcaatgataccgcgagacccacgctcaccggctccagatttatcagcaataaaccagccagccggaagggccgagcgcagaagtggtcctgcaactttatccgcctccatccagtctattaattgttgccgggaagctagagtaagtagttcgccagttaatagtttgcgcaacgttgttgccattgctacaggcatcgtggtgtcacgctcgtcgtttggtatggcttcattcagctccggttcccaacgatcaaggcgagttacatgatcccccatgttgtgcaaaaaagcggttagctccttcggtcctccgatcgttgtcagaagtaagttggccgcagtgttatcactcatggttatggcagcactgcataattctcttactgtcatgccatccgtaagatgcttttctgtgactggtgagtactcaaccaagtcattctgagaatagtgtatgcggcgaccgagttgctcttgcccggcgtcaatacgggataataccgcgccacatagcagaactttaaaagtgctcatcattggaaaacgttcttcggggcgaaaactctcaaggatcttaccgctgttgagatccagttcgatgtaacccactcgtgcacccaactgatcttcagcatcttttactttcaccagcgtttctgggtgagcaaaaacaggaaggcaaaatgccgcaaaaaagggaataagggcgacacggaaatgttgaatactcatactcttcctttttcaatattattgaagcatttatcagggttattgtctcatgagcggatacatatttgaatgtatttagaaaaataaacaaataggggttccgcgcacatttccccgaaaagtgccacctgacgtctaagaaaccattattatcatgacattaacctataaaaataggcgtatcacgaggccctttcgtctcgcgcgtttcggtgatgacggtgaaaacctctgacacatgcagctcccggagacggtcacagcttgtctgtaagcggatgccgggagcagacaagcccgtcagggcgcgtcagcgggtgttggcgggtgtcggggctggcttaactatgcggcatcagagcagattgtactgagagtgcaccataacgcatttaagcataaacacgcactatgccgttcttctcatgtatatatatatacaggcaacacgcagatataggtgcgacgtgaacagtgagctgtatgtgcgcagctcgcgttgcattttcggaagcgctcgttttcggaaacgctttgaagttcctattccgaagttcctattctctagctagaaagtataggaacttcagagcgcttttgaaaaccaaaagcgctctgaagacgcactttcaaaaaaccaaaaacgcaccggactgtaacgagctactaaaatattgcgaataccgcttccacaaacattgctcaaaagtatctctttgctatatatctctgtgctatatccctatataacctacccatccacctttcgctccttgaacttgcatctaaactcgacctctacattttttatgtttatctctagtattactctttagacaaaaaaattgtagtaagaactattcatagagtgaatcgaaaacaatacgaaaatgtaaacatttcctatacgtagtatatagagacaaaatagaagaaaccgttcataattttctgaccaatgaagaatcatcaacgctatcactttctgttcacaaagtatgcgcaatccacatcggtatagaatataatcggggatgcctttatcttgaaaaaatgcacccgcagcttcgctagtaatcagtaaacgcgggaagtggagtcaggctttttttatggaagagaaaatagacaccaaagtagccttcttctaaccttaacggacctacagtgcaaaaagttatcaagagactgcattatagagcgcacaaaggagaaaaaaagtaatctaagatgctttgttagaaaaatagcgctctcgggatgcatttttgtagaacaaaaaagaagtatagattctttgttggtaaaatagcgctctcgcgttgcatttctgttctgtaaaaatgcagctcagattctttgtttgaaaaattagcgctctcgcgttgcatttttgttttacaaaaatgaagcacagattcttcgttggtaaaatagcgctttcgcgttgcatttctgttctgtaaaaatgcagctcagattctttgtttgaaaaattagcgctctcgcgttgcatttttgttctacaaaatgaagcacagatgcttcgttgcttgcatgcaacttcttttctttttttttcttttctctctcccccgttgttgtctcaccatatccgcaatgacaaaaaaaatgatggaagacactaaaggaaaaaattaacgacaaagacagcaccaacagatgtcgttgttccagagctgatggaggggtatcttcgaacacacgaaactttttccttccttcattcacgcacactactctctaatgagcaacggtatacggccttccttccagttacttgaatttgaaataaaaaaagtttgccgctttgctatcaagtataaatagacctgcaattattaatcttttgtttcctcgtcattgttctcgttccctttcttccttgtttctttttctgcacaatatttcaagctatatccaagcatacaatcaactccaagctttgcaaagatggataaagcggaattaattcccgagcctccaaaaaagaagagaaaggtcgaattgggtaccgccgccaattttaatcaaagtgggaatattgctgatagctcattgtccttcactttcactaacagtagcaacggtccgaacctcataacaactcaaacaaattctcaagcgctttcacaaccaattgcctctctaacgttcatgataacttcatgaataatgaaatcacggctagtaaaattgatgatggtaataattcaaaaccactgtcacctggttggacggaccaaactgcgtaataacgcgtttggaatcactacagggatgtttaataccactacaatggatgatgtatataactatctattcgatgatgaagataccccaccaaacccaaaaaaagagatcgaattcttaatacgactcactatagggcccatggacgaagaatccagttcattcttatgtacctatgctgagaatcgtgccaataagaagccaatacttccttagatgatgcaataaatattaaaataaaacaaaacagaaggctgpGN205:                                           SEQUENCE ID NO.10ccggtggtaccgggccccccctcgaggtcgacggtatcgataagctttcgtcattgaaaagaaggataagaatggacgatgggaagaagctctcgttgttccaggagatcagaaaacagcaactgttccaaatcttaaggagggagaagaatatcaattcagaatttctgctcgtaacaaggctggaactggagatccttctgatccttctgatcgtgttgttgcgaagccaagaaaccttgctccaagaattcatcgtgaagatctttctgatacaactgtcaaggtcggagccactctcaagttcattgttcatattgatggtgagccagcaccagatgtaacatggtcattcaatggaaaaggaatcggagagagcaagactcaaattgaaaatgagccatacatctcgagatttgctttgccaaaggcacttcgtaagcaaagtggaaaatataccatcactgcaaccaacattaatggaactgacagtgtcactatcaatatcaaggtaaaaagcaagccaacgaaaccaaagggaccaatcgaggtaactgatgtcttcgaagatcgtgcaactcttgactggaaaccaccagaggatgacggaggagagccaattgagttctatgaaattgaaaagatgaacaccaaggacggaatctgggttccatgtggacgtagtggagatacccacttcacagtcgattcactcaacaagggagatcattacaagttccgtgtcaaggctgtcaacagcgaaggacctcctgatccattggaaactgaaaccgatattttggctaaaaatccatttgatcgtccagatagaccaggtcgtccagagccaactgattgggattctgatcatgttgatctcaagtgggatccactagttctagaagcgctgctaagggggccctcgtcgagtcggtcacaatcacctgaaactccaaaggcagccagtgaggaacgtgaagaagaagaaaaagagtcatctgaacaggtttgattttctttctggtcaaaaagatgaaattattgattttcagccagatactcccaaaactagcagcgagaagtctgcaagtcgttcacagtcgcccagagaatcgcgggaagtgagccaagaggtatgtttttcaaaaatcaataactgatcataatttttattgtttggtgaatttaagaaaataatattcgaaaattcctctgaattatcaagattgcagtattaatttcgagaaaaattgagatattcatagagctattgtaaattttcttgatttcagactgaaacttcggaaaatcaagagaaaatcaaagaaaaggatgacggggatgatcagcctggcacaccgaacagctatagaagccgggaaacttcaccagctccaaaaaggtccaaggagaccaggtttgtcaaaagcttcctgcgattaattctcatttcaatttttcagagaatcagagtctcctgaaaaatccccggttcgttcaagatctcccagaaggtcttcagcacgttccccgtcacgatctcctagacggcgccgagaaagaagctcagaaagaaagcaatccgaagagccagcaccgctaccagagaaaaagaagaaagagccgctggatattctacgaacaagaaccggaggagcatatattccacccgccaaacttcgacttatgcaacaacagattagtgataagcaaagtgaacagtatcagagaatgaattgggaaagaatgaagaaaaagattcacggattggttaacagagtcaacgcgaagaatcttgttcaaattgtcagagaacttcttcaagagaatgtgattcgttcaaagtgagtgagaaaatcgaaggaaaaggaaagaattaatttaatttttcaggggacttctctgccgtgacattattcaagctcaggctttctcaccaggattctctaacgtctatgcagctttggcggcagttatcaactcgaaattccctcatgtcggtgaacttcttctccgtcgtctgattgtacagttcaaaagaagtttccgtagaaatgacagaggcgtcacggtgaacgtgatcaaattcatcgcacatttgattaatcaacaagttgctcacgaagttcttgcgctggaaatcatgattctgatgcttgaagaaccaactgatgattcagttgaagtcgccattgcgttcctgaaagagtgtggagcaaagcttctggagattgctccagcagctcttaacagtgtctacgaccgtcttcgtgcaattctcatggaaactgaaagatcggaaaatgcactggatcgacgtattcagtatatgattgagactgcaatgcagattcgaaaggacaaatttgcggtaaggtagaatatataaatagtttattagaaaaaaataaattagaataatttaaattcctactagccaatcaggcgacctttttgcgcatagttctattattgaaaaatttggagaatttctcatattctcgctcggaaatctggaattcgacgagatcttctggcttctgtgcagctgcatcgctttgtgctccctttctcgcttgtcttctgtgtacaccaagaaccttgttgagttcatcaactgaatctgtgactggcttgttgctcactggatgcactagacgactgattctcgagaaatcagattgagttgcgattagggtgacctagaaattgggaataatacgaacttttgaaaatattcaggaggattaaaaaaattattctcgacaatcctacaaatttcttattgcaccatgttgctccaacatttttcattaaaagttaatgaaaaaatgtagaaaatcggaaattggcaattttcagaccatttttaagcattttcaaaaaaaaattgcagctgaaataaatgtcattttcagataaatcgagcgattttctgttgtctgacactagtttttagttttaaaaaatgttggaagaacatggtgcaataggtaatttcatagaatttccatgtgttttttttcaattaaccaattatccaaatcttccaaactcacattttgcggagctgggctatcaagaatctgctgcagttttataagacgagcatctctgatatcactgaaaattaatttttaatcaaaacttgaatatcaactaaacccacttattaactttctcgatcttctgtcgttcggtacgatgacggtgaagaagccaattgtagtagttgatttggttcaagtcctttcggtgttgtacgtcagtgtcctgcaatgctatttagttataacttaggcctaagattcaatttaatgaagtgattaaatttgttctctgaacctcttaagatgatcttttggattagaaacatataagacaggtttacctatctattaaaaaacagatcaaaatagatacgccaaatcggataatccatgcctacctggcatctaggaacgtgttcttagaagatttcttacgtaatcgtatgaagaaataacaatttgatcgttggccagcaaaaatagggttttaagtgggatagtgtttttattagctaaccggaaaattttatagtttttttttgcaagaaaccactgaaaaccccctaattgtatacattttggagcagcttctggtctttttgagcaataaaattcgataaaacagaatttaagtgtaaattgttcacatttagtttctattttatcaaattttgttgctcaaaaacattcgaagctgctctaaaaaaatgcattaaaaaaggggttttcagtggtttttcacattaaaaaagctaattttaactaaaaatccatcatatttccaactttgtcacaacaataaaatgctggtcaaaatgtgttcgaaaaaatgtttttttttttaatttttataatttaaaaatagttttctttcgctgggacacatacatttttgggcgtaaattttcagttcaaatttccatttttacaaccataatcataaagctacgtctgtctctctcgcacttacctgcgcctgattcgaaagaacaaccgtagccaaaagaacaagaagaacaagcacgtagttgtggtagtggacgttcatcacgcaatactgaccaatggtcgtggggtctcactttccgtactattgagagaggggagactgaagatggcaattgaggacagtgtcttcgacgcacgcatgcatccataagcataatccaggagggatggagagaaaaatcttgtttctaagcccctccctttgtaatacatacacatatctaataccgaagaatggctaattgaatggacgtcagctgttgctgtagttgccaaggcatcatcgatgaaataactgaaagaaagaattaaataattattgcaggcgtatccggcggtcattgaagacttggacttgattgaggaggaggatcagatcatccatacacttaatttggaggatgcggttgatccggaaaatgggcttagtaagtgactgaccacacgcggggggcattaatttaataaattgaattccatttcagatgtgttcaaactagatccagaattcgaaaagaacgaggaggtttatgaggagatccgtaaggaaatcattggaaacgccgatatttcggatgaggatggtggcgacgagttggatgatgaagaagagggtagtgatgtggaagaggctccgaagaagactacagagattattgataatactgatcagaattgactgctttcagaaggtattcattttgagttttgggccggcaaatctgtaagttgccggttgccgaaaatttgctgaatttgccggaaaaaaaaattccggaatttatttaaaaactttttgtaaaaattaaattaaatttgcaacttttcagagaagtctacctgacaatgcaatcatctttggactaccaagaagctgctcacaaattgctgaaaatgaagattccagacagcatgcaggtcagcgatgttgcaaagaaaaattttcgaccaaaaaaaccaaccaatcataaaatttaaaaaaaaactccgtttttttctttttttttatacgagaaaaaccaaaaaaatgtatttttgccaaattctaaaatactatccccgaaattttcaatattttctctttcagaacgaactctgcgcgatgcttgtcgattgttgtgctcaacagcgtacctacgagcgattctacggaatgctcatcgaacgtttctgccgacttcgcctcgaataccagcaatactttgaaaagctctgccaggacacgtattccacgattcaccgaattgacatcacaaaactgcggaatttggctcgccttattgctcatttgctctcgacggatgctattgactggaagattttggccgatatgaaaatgaccgaagaggacacaacttcttctggcagaatctatattaaatatatatttaatgaacttgtggaggcgatgggaatggttaaacttcattcgagagttactgatccgtgagtttcctagagagagttgttttcgtattcaattttccctattttcagaactttggctcattgctttgttggattattcccacgaactaatccgaacagcgcacgattttcgatcaacttcttcacaatgattggattgggtggttgacgttggaacttcgtgaatggctggcaaagggtctcaagaagaagaagggaatgctggatcagttgaaggccgaatcaagctcagattcatcgtcgtcttcggattcgtcagactcgtctgattcttcggattctgacgattcatccgactcgtcttcagattcctcatcttcttcagaatcagagccagaaccaccgaagaaaaagaagaagaagaacagtgaagagagttccaaaaagaaggaaaaagagaatattggtcgacgggatcgtggagacaagagagctgaacgtcatcgtgatcaaagtgtggagaacaaggacaaggatcgtcgacgtcgccaggattctgacgaaaatcgtcggccagaacgaggagatgaccgcaaggatcggagtaaagatcgtcgtcgtcaagactcggatgatgaggatcggaaaggtcgtgaacgtcgggaagattcaggggaa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Claims (90)

1.负责在细胞中赋予特定表型的DNA的鉴定方法,所述方法包括:
a)以相应于启动子、当合适的转录因子结合于所述启动子时能够启动从所述cDNA或DNA转录出双链(ds)RNA的方向,在合适的载体中构建所述细胞DNA的cDNA文库或基因组文库,
b)将所述文库引入包含所述转录因子的一种或多种所述细胞中,且
c)鉴定和分离包含所述文库的特定表型的所述细胞,并鉴定所述文库中负责赋予所述表型的DNA或cDNA片段。
2.按照权利要求1的方法,其中在步骤b)之前,将所述文库组成为等级库。
3.将功能确定到已知DNA序列的方法,所述方法包括:
a)鉴定细胞中所述DNA序列的同源物,
b)从所述细胞中分离出相关的DNA同源物或其片段,
c)将所述同源物或其片段以相应于合适启动子、当合适的转录因子结合于所述启动子时能够启动从所述DNA同源物或其片段转化dsRNA的方向,克隆到合适的载体中,
d)将所述载体引入得自步骤a)的包含所述转录因子的所述细胞中,且
e)鉴定与野生型相比的所述细胞的表型。
4.根据权利要求1-3中任一项的方法,其中将所述DNA文库、同源物或片段以相应于所述启动子的有义和反义的方向克隆。
5.根据权利要求1-3中任一项的方法,其中将所述DNA文库、同源物或片段克隆在两个启动子之间,使得当合适的转录因子结合于所述启动子时能够从所述DNA文库、同源物或片段产生dsRNA。
6.根据权利要求1-5中任一项的方法,其中所述细胞被改变以表达所述转录因子。
7.根据权利要求1-6中任一项的方法,其中将所述DNA文库、同源物或片段构建在合适的载体中,所述载体包含一段有效连接至合适启动子的编码所述转录因子的核苷酸序列。
8.根据权利要求1-6中任一项的方法,其中所述转录因子由另一载体编码,所述另一载体与包含所述DNA文库、同源物或片段无关的载体,并且编码所述转录因子的序列有效连接至合适的启动子。
9.根据权利要求7或8的方法,其中所述转录因子包括T7、T3或SP6聚合酶中的任一种。
10.根据权利要求7或8的方法,其中所述合适的启动子包括let858、SERCA、UL6、myo-2或myo-3中的任一种。
11.根据权利要求7-10中任一项的方法,其中所述合适的载体或所述另一载体包含一个选择标记。
12.根据权利要求11的方法,其中所述选择标记包含能够抑制或防止基因在所述细胞中表达的核苷酸序列,而所述基因负责赋予一种已知表型。
13.根据权利要求12的方法,其中所述核苷酸序列包含的一段序列是赋予所述表型的所述基因的一部分,或与所述基因相同,而所述核苷酸序列本身的定向与在合适的转录因子结合于所述启动子时能够启动双链RNA转录的合适启动子相应。
14.根据权利要求12的方法,其中所述核苷酸序列是赋予所述表型的所述基因序列的一部分,或与所述基因序列相同,而所述核苷酸序列是这样的序列,以致允许所述合适的载体或另一载体通过同源重组整合到所述细胞的基因组中,并且在所述整合后,所述核苷酸序列能够抑制赋予所述表型的所述基因序列的表达。
15.根据权利要求14的方法,其中所述核苷酸序列包含足以防止所述核苷酸序列在其整合到所述基因组中之后进行翻译的终止密码子。
16.根据任一前述权利要求的方法,其中所述细胞为适合于饲喂、转化或感染生物的微生物。
17.根据权利要求1-14中任一项的方法,其中所述细胞包含于生物或其胚胎中。
18.根据权利要求1-17中任一项的方法,其中所述启动子为T7启动子。
19.根据权利要求12-18中任一项的方法,其中所述已知基因序列包括sup-35基因或其片段,在将所述载体引入pha-1 et123ts突变C.elegans蠕虫的基因座中之后,通过鉴定在高于25℃的温度下生长的后代,可选择出所述基因或其片段。
20.根据权利要求1-19中任一项的方法,其中使所述细胞或生物与用于筛选所需表型的所述化合物接触,所述表型诸如当与野生型细胞或生物相比时对所述化合物的抗性或敏感性。
21.根据任一前述权利要求的方法,其中所述转录因子是可诱导的。
22.根据权利要求16的方法,其中所述微生物为RNA酶Ⅲ阴性、且最好为RNA酶阴性的大肠杆菌菌株。
23.根据权利要求17的方法,其中所述生物选自线虫纲。
24.根据权利要求23的方法,其中所述生物为Caenorhabditiselegans。
25.产生包含一种外源转录因子和一种转基因的转基因非人类生物的方法,其中所述转基因包含一个有效连接至DNA片段的启动子,当所述转录因子结合于启动子时,表达所述DNA片段;所述方法包括:
a)提供包含第一构成物的第一转基因生物和包含第二构成物的第二转基因生物,所述第一构成物加入了编码外源转录因子的DNA,而所述第二构成物包括至少一个有效连接至所需DNA序列的启动子,在所述第一转基因生物的所述转录因子结合于所述启动子时,表达所需DNA序列。
b)将所述第一转基因生物与所述第二转基因生物杂交,并选择表达所述所需DNA序列的后代。
26.根据权利要求25的方法,其中通过将所述第一和第二构成物转化到相应的微生物中,随后用所述微生物饲喂所述相应的生物,来产生所述第一和第二转基因生物。
27.根据权利要求25或26的方法,其中所述第二构成物包含所述所需DNA序列,所述所需DNA序列相应于所述启动子的方向,使得可以当所述转录因子结合于所述启动子时,能够启动从所述DNA转录出dsRNA。
28.根据权利要求27的方法,其中所述第二构成物包含两个邻接所述所需DNA序列的启动子,所述启动子在所述转录因子与其结合时,可以启动从所述DNA序列转录出dsRNA。
29.根据权利要求27的方法,其中以相应于所述启动子的有义和反义的方向提供所述DNA序列,使得在所述转录因子结合于所述启动子时产生dsRNA。
30.根据权利要求25-29中任一项的方法,其中所述第二转基因生物还包含一个有效连接至启动子的报道基因,所述启动子在所述转录因子与其结合时能够启动所述报道基因的转录。
31.根据权利要求25-30中任一项的方法,其中所述转录因子包括聚合酶。
32.根据权利要求31的方法,其中所述聚合酶包括T7、T3或SP6聚合酶中的任一种。
33.根据权利要求25-31中任一项的方法,其中所述启动子包括T7、T3或SP6启动子中的任一种。
34.根据权利要求30的方法,其中所述报道基因包括包括荧光素酶、绿荧光蛋白、β半乳糖苷酶或β-内酰胺酶的编码序列中的任一种。
35.根据权利要求25-30中任一项的方法,其中所述生物为线虫纲物种的生物。
36.根据权利要求35的方法,其中所述线虫纲物种为C.elegans。
37.根据权利要求25-34中任一项的方法可获得的转基因非人类多细胞生物。
38.在酵母双杂种载体实验所鉴定的克隆的验证方法,所述方法包括:
a)提供一种构成物,所述构成物包含在双杂种载体实验中所鉴定的蛋白的编码DNA,所述构成物使得所述DNA以相应于一个或多个启动子的方向定向,在合适的转录因子结合于所述启动子时,所述启动子能够启动从所述DNA转录出双链RNA,
b)用所述构成物转化包含所述转录因子的细胞,并且
c)鉴定在所述细胞或生物中与野生型相比的表型变化。
39.根据权利要求38的方法,其中在两个启动子之间提供所述DNA序列,所述启动子在所述转录因子结合于所述启动子时,能够启动从所述DNA序列转录出dsRNA。
40.根据权利要求38的方法,其中以相应于所述启动子的有义和反义的方向提供所述DNA,使得合适的转录因子与所述启动子的结合,启动从所述DNA转录出dsRNA。
41.根据权利要求38-40中任一项的方法,其中所述转录因子在所述细胞中是可诱导的。
42.根据权利要求38-41中任一项的方法,其中所述启动子为噬菌体聚合酶启动子,而所述转录因子为RNA聚合酶。
43.根据权利要求42的方法,其中所述聚合酶为T7RNA聚合酶、T3RNA聚合酶或SP6RNA聚合酶中的任一种。
44.根据权利要求43的方法,其中所述启动子包括T7、T3或SP6启动子中的任一种。
45.根据权利要求38-44中任一项的方法,其中所述构成物使得它可以用于酵母双杂种实验。
46.根据权利要求38-45中任一项的方法,其中所述细胞为大肠杆菌细胞。
47.根据权利要求38-45中任一项的方法,其中所述细胞为生物或其胚胎的一部分。
48.根据权利要求47的方法,其中所述生物为线虫纲物种的生物,最好为C.elegans。
49.在图1中图解的质粒pGN1。
50.在图2中图解的质粒pGN100。
51.在图4、15或16(Sequence ID No 8和9)的任一个中图解的酵母双杂种载体质粒。
52.在图7中图解的质粒。
53.在图8中图解的质粒。
54.减轻植物害虫侵染的方法,所述方法包括:
a)从所述害虫中鉴定出对其生存、生长、增殖重要的DNA序列,
b)在合适的载体中,以相对于启动子的方向克隆得自步骤a)的所述序列或其片段,所述启动子在合适的转录因子与其结合时能够启动从所述DNA序列转录出RNA或dsRNA,并且
c)将所述载体引入所述植物中。
55.根据权利要求54的方法,其中在两个启动子之间提供所述DNA序列,使得所述转录因子结合于所述启动子,导致从所述DNA序列转录出dsRNA。
56.根据权利要求54的方法,其中以相应于所述启动子的有义和反义的方向提供所述DNA,使得所述转录因子结合于所述启动子,导致从所述DNA转录出dsRNA。
57.根据权利要求54的方法,其中所述害虫为线虫蠕虫。
58.根据权利要求57的方法,其中所述线虫包括小垫刃线虫属物种(Tylenchulus ssp.)、穿孔线虫属物种(Radopholus ssp.)、细杆滑刃线虫属物种(Rhadinaphelenchus ssp.)、异皮线虫属物种(Heterodera ssp.)、小盘旋线虫属物种(Rotylenchulus,ssp.)、短体线虫属物种(Pratylenchusssp.)、刺线虫属物种(Belonolaimus ssp.)、Canjanus ssp.、根结线虫属物种(Meloidogyne ssp.)、球异皮线虫属物种(Globodera ssp.)、科布线虫属物种(Nacobbus ssp.)、茎线虫属物种(Ditylenchus ssp.)、滑刃线虫属物种(Aphelenchoides ssp.)、潜根线虫属物种(Hirschmenniella ssp.)、鳗线虫属物种(Anguina ssp.)、纽带线虫属物种(Hoplolaimus ssp.)、螺旋线虫属物种(Heliotylenchus ssp.)、小环线虫属物种(Criconemella ssp.)、剑线虫属物种(Xiphinema ssp.)、长针线虫属物种(Longidorus ssp.)、毛刺线虫属物种(Trichodorus ssp.)、副毛刺线虫属物种(Paratrichodorus ssp.)、真滑刃线虫属物种(Aphelenchs ssp.)中的任一种。
59.根据权利要求55的方法,其中将所述DNA序列或其片段克隆在两个组织特异性启动子之间,最好是克隆在两个根特异性启动子之间。
60.用于按照任一前述权利要求的方法的表达载体,所述载体包含一个或多个启动子,所述启动子相对于DNA序列的定向使得在合适的转录因子结合于所述一个或多个启动子时,所述启动子能够启动从所述DNA序列转录出双链RNA。
61.根据权利要求60的表达载体,其包含两个邻接所述DNA序列的相同的启动子。
62.根据权利要求60的表达载体,其包含相对于所述启动子为有义和反义方向的所述DNA。
63.根据权利要求60-62中任一项的表达载体,其还包含一段编码选择标记的核苷酸序列。
64.根据权利要求63的表达载体,其中将编码所述选择标记的所述核苷酸序列相对于所述启动子的定向,使得在合适的转录因子结合于所述启动子时,发生从所述核苷酸序列转录出双链RNA。
65.根据权利要求64的表达载体,其中在两个相同的启动子之间提供编码所述选择标记的所述核苷酸序列,所述启动子在所述转录因子结合于所述启动子时,能够启动从所述核苷酸序列转录出dsRNA。
66.根据权利要求64的表达载体,其中以相对于所述启动子的有义和反义方向提供编码所述选择标记的所述核苷酸序列,使得在合适的转录因子结合于所述启动子时,从所述核苷酸序列转录出双链RNA。
67.根据权利要求63或64的表达载体,其中所述选择标记包含一段编码sup-35的核苷酸序列,用于引入具有pha-1突变的C.elegans中。
68.表达载体,用于表达用于按照权利要求1-48和54-59中任一项的方法中的合适的转录因子,所述载体包含一段有效连接至合适的表达控制序列的、编码所述转录因子的核苷酸序列。
69.根据权利要求68的表达载体,其中所述表达控制序列包括诱导型启动子、组成型启动子、普遍性启动子或组织特异性启动子或它们的组合。
70.根据权利要求68-69中任一项的表达载体,其中所述转录因子包括噬菌体聚合酶,最好是T7 RNA聚合酶。
71.用根据权利要求49-53中任一项的质粒或用根据权利要求60-70中任一项的表达载体转化或转染的生物或细胞。
72.根据权利要求71的生物,其中所述生物为线虫纲物种的生物,最好是C.elegans。
73.将dsRNA或将能够产生dsRNA的DNA引入生物中的方法,所述方法包括用包含根据权利要求60-67中任一项的表达载体的合适微生物饲喂所述生物,或用根据权利要求60-67中任一项的表达载体直接饲喂所述生物。
74.根据权利要求73的方法,其中所述微生物或所述生物被改变以表达所述转录因子。
75.根据权利要求74的方法,其中或者所述微生物或者所述生物包含根据权利要求66-69中任一项的表达载体。
76.根据权利要求73-75中任一项的方法,其中所述生物为C.elegans,而所述微生物是大肠杆菌。
77.根据权利要求76的方法,其中所述大肠杆菌菌株为RNA酶Ⅲ阴性菌株。
78.根据权利要求73-75中任一项的方法,其中所述生物为C.elegans nuc-1突变体。
79.选择系统,用于鉴定用根据权利要求60-63的载体对细胞或生物的转化,所述系统包括一个根据权利要求60-63的载体,而所述选择标记包括一段在所述细胞或生物中能够抑制或防止负责赋予已知表型的基因表达的核苷酸序列。
80.根据权利要求79的选择系统,其中所述核苷酸序列包含的一段序列是赋予所述已知表型的所述基因的一部分,或与所述基因相同,而所述核苷酸序列本身位于两个相同启动子之间,所述启动子在合适的转录因子结合于所述启动子时,能够启动转录双链RNA转录。
81.根据权利要求79的选择系统,其中所述核苷酸序列是赋予所述细胞或生物已知表型的所述基因的一部分,或与所述基因相同,并且所述核苷酸序列允许所述载体通过同源重组整合到所述细胞或生物的染色体中,并且在所述整合后,所述序列抑制赋予所述已知表型的所述基因序列的表达。
82.根据权利要求81的选择系统,其中所述核苷酸序列包含足以防止所述核苷酸序列在整合到所述基因组中后翻译的终止密码子。
83.根据权利要求79的选择系统,其中所述已知基因序列包含sup-35基因或其片段,在将所述载体引入pha-1 et123ts突变型C.elegans蠕虫中之后,通过鉴定在高于25℃的温度下生长的后代,可选择出所述基因或其片段。
84.根据权利要求74的方法,其中所述转录因子为T7RNA聚合酶。
85.将功能确定到多细胞生物的DNA序列的方法,所述方法包括:
a)将以下构成物:
ⅰ)第一构成物,包含以有义方向克隆的、在合适的启动子调节下的所述DNA序列,
ⅱ)第二构成物,包含以反义方向克隆的、在与步骤(ⅰ)中的相同启动子调节下的所述DNA序列,
提供到多细胞生物中,所述多细胞生物被改变以启动从合适的启动子转录所述DNA片段,
b)鉴定与野生型相比的所述多细胞生物的表型。
86.将功能确定到给多细胞生物的DNA序列的方法,所述方法包括:
a)在多细胞生物中提供:
ⅰ)第一构成物,包含在两个能够在所述多细胞生物中启动转录的启动子之间克隆的所述DNA片段,
所述多细胞生物能够启动从合适的启动子转录所述DNA片段,
b)鉴定与野生型相比的所述多细胞生物的表型。
87.在C.elegans中表达基因、cDNA或DNA片段的方法,所述方法包括:
ⅰ)提供表达外源转录因子的转基因C.elegans,
ⅱ)将所述基因或cDNA或DNA片段克隆到合适的载体中,与在所述外源转录因子与启动子结合时能够启动所述基因、cDNA或DNA片段转录的启动子有效连接,
ⅲ)将所述载体引入得自步骤ⅰ)的所述转基因C.elegans中。
88.根据权利要求87的方法,其中所述外源转录因子为噬菌体聚合酶。
89.根据权利要求88的方法,其中所述噬菌体聚合酶为T3、SP6或T7 RNA聚合酶。
90.根据权利要求87-89中任一项的方法,其中所述启动子为T7、T3或SP6启动子中的任一种。
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107858405A (zh) * 2017-10-12 2018-03-30 华南农业大学 一种测定外源dsRNA对瓢虫毒性影响的方法
CN110746497A (zh) * 2019-11-18 2020-02-04 维塔恩(广州)医药有限公司 肺炎衣原体相关抗原短肽及其应用
CN110804088A (zh) * 2019-11-18 2020-02-18 维塔恩(广州)医药有限公司 巨细胞病毒相关抗原短肽及其应用

Families Citing this family (251)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6506559B1 (en) 1997-12-23 2003-01-14 Carnegie Institute Of Washington Genetic inhibition by double-stranded RNA
AUPP249298A0 (en) * 1998-03-20 1998-04-23 Ag-Gene Australia Limited Synthetic genes and genetic constructs comprising same I
CN101818145A (zh) 1998-03-20 2010-09-01 联邦科学和工业研究组织 控制基因表达
GB9827152D0 (en) * 1998-07-03 1999-02-03 Devgen Nv Characterisation of gene function using double stranded rna inhibition
EP1147204A1 (en) * 1999-01-28 2001-10-24 Medical College Of Georgia Research Institute, Inc. Composition and method for in vivo and in vitro attenuation of gene expression using double stranded rna
DE19956568A1 (de) 1999-01-30 2000-08-17 Roland Kreutzer Verfahren und Medikament zur Hemmung der Expression eines vorgegebenen Gens
US7601494B2 (en) 1999-03-17 2009-10-13 The University Of North Carolina At Chapel Hill Method of screening candidate compounds for susceptibility to biliary excretion
IL145778A0 (en) * 1999-04-21 2002-07-25 American Home Prod Methods and compositions for inhibiting the function of polynucleotide sequences
US20040138168A1 (en) * 1999-04-21 2004-07-15 Wyeth Methods and compositions for inhibiting the function of polynucleotide sequences
US6924109B2 (en) * 1999-07-30 2005-08-02 Agy Therapeutics, Inc. High-throughput transcriptome and functional validation analysis
US6423885B1 (en) 1999-08-13 2002-07-23 Commonwealth Scientific And Industrial Research Organization (Csiro) Methods for obtaining modified phenotypes in plant cells
WO2001029058A1 (en) 1999-10-15 2001-04-26 University Of Massachusetts Rna interference pathway genes as tools for targeted genetic interference
GB9927444D0 (en) * 1999-11-19 2000-01-19 Cancer Res Campaign Tech Inhibiting gene expression
DE10100586C1 (de) 2001-01-09 2002-04-11 Ribopharma Ag Verfahren zur Hemmung der Expression eines Ziegens
US7829693B2 (en) 1999-11-24 2010-11-09 Alnylam Pharmaceuticals, Inc. Compositions and methods for inhibiting expression of a target gene
GB9930691D0 (en) * 1999-12-24 2000-02-16 Devgen Nv Improvements relating to double-stranded RNA inhibition
US8202979B2 (en) 2002-02-20 2012-06-19 Sirna Therapeutics, Inc. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid
US7491805B2 (en) 2001-05-18 2009-02-17 Sirna Therapeutics, Inc. Conjugates and compositions for cellular delivery
US7833992B2 (en) 2001-05-18 2010-11-16 Merck Sharpe & Dohme Conjugates and compositions for cellular delivery
US8273866B2 (en) 2002-02-20 2012-09-25 Merck Sharp & Dohme Corp. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (SINA)
IL151781A0 (en) 2000-03-16 2003-04-10 Genetica Inc Methods and compositions for rna interference
US8202846B2 (en) 2000-03-16 2012-06-19 Cold Spring Harbor Laboratory Methods and compositions for RNA interference
WO2001075164A2 (en) 2000-03-30 2001-10-11 Whitehead Institute For Biomedical Research Rna sequence-specific mediators of rna interference
GB2362383B (en) * 2000-05-19 2003-12-31 Devgen Nv Gene expression system
GB0012233D0 (en) 2000-05-19 2000-07-12 Devgen Nv Vector constructs
GB0012229D0 (en) 2000-05-19 2000-07-12 Devgen Nv Lipid uptake assays
US7083947B2 (en) 2000-05-19 2006-08-01 Devgen Nv Assay techniques using nematode worms
WO2001096584A2 (en) * 2000-06-12 2001-12-20 Akkadix Corporation Materials and methods for the control of nematodes
US20030190635A1 (en) * 2002-02-20 2003-10-09 Mcswiggen James A. RNA interference mediated treatment of Alzheimer's disease using short interfering RNA
DK2813582T3 (en) 2000-12-01 2017-07-31 Max-Planck-Gesellschaft Zur Förderung Der Wss E V Small RNA molecules that mediate RNA interference
US7423142B2 (en) 2001-01-09 2008-09-09 Alnylam Pharmaceuticals, Inc. Compositions and methods for inhibiting expression of anti-apoptotic genes
US8546143B2 (en) 2001-01-09 2013-10-01 Alnylam Pharmaceuticals, Inc. Compositions and methods for inhibiting expression of a target gene
US7767802B2 (en) 2001-01-09 2010-08-03 Alnylam Pharmaceuticals, Inc. Compositions and methods for inhibiting expression of anti-apoptotic genes
BR0206690A (pt) 2001-01-25 2006-01-17 Virxsys Corp Processos para a identificação da função do gene, para alteração da expressão de fatores celulares e para alteração do fenótipo de célula
JP4454934B2 (ja) 2001-01-26 2010-04-21 コモンウェルス サイエンティフィック アンド インダストリアル リサーチ オーガニゼイション 組換えクローニングを用いて効率のよいサイレンシング構築物を作製する方法および手段
EP1229134A3 (en) 2001-01-31 2004-01-28 Nucleonics, Inc Use of post-transcriptional gene silencing for identifying nucleic acid sequences that modulate the function of a cell
EP1364066A2 (en) * 2001-02-02 2003-11-26 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Method for identifying functional nucleic acids
US9994853B2 (en) 2001-05-18 2018-06-12 Sirna Therapeutics, Inc. Chemically modified multifunctional short interfering nucleic acid molecules that mediate RNA interference
US20050148530A1 (en) 2002-02-20 2005-07-07 Sirna Therapeutics, Inc. RNA interference mediated inhibition of vascular endothelial growth factor and vascular endothelial growth factor receptor gene expression using short interfering nucleic acid (siNA)
WO2003070888A2 (en) * 2002-02-20 2003-08-28 Sirna Therapeutics, Inc. Rna interference mediated inhibition of checkpoint kinase-1 (chk-1) gene expression using short interfering nucleic acid
JP4358521B2 (ja) 2001-05-18 2009-11-04 サーナ・セラピューティクス・インコーポレイテッド 細胞デリバリーのためのコンジュゲートおよび組成物
WO2003102131A2 (en) * 2002-04-22 2003-12-11 Sirna Therapeutics Inc. Nucleic acid mediated disruption of hiv fusogenic peptide interactions
US7109165B2 (en) 2001-05-18 2006-09-19 Sirna Therapeutics, Inc. Conjugates and compositions for cellular delivery
JP4210737B2 (ja) 2001-07-12 2009-01-21 ユニバーシティー オブ マサチューセッツ 遺伝子サイレンシングを仲介する低分子干渉リボ核酸のインビボにおける製造方法
US7612194B2 (en) * 2001-07-24 2009-11-03 Monsanto Technology Llc Nucleic acid sequences from Diabrotica virgifera virgifera LeConte and uses thereof
EP1431392B1 (en) * 2001-08-31 2010-04-21 Riken PLANT SYSTEM FOR COMPREHENSIVE GENE FUNCTION ANALYSIS WITH THE USE OF FULL-LENGTH cDNA
DE10163098B4 (de) 2001-10-12 2005-06-02 Alnylam Europe Ag Verfahren zur Hemmung der Replikation von Viren
US7745418B2 (en) 2001-10-12 2010-06-29 Alnylam Pharmaceuticals, Inc. Compositions and methods for inhibiting viral replication
US20030150017A1 (en) * 2001-11-07 2003-08-07 Mesa Jose Ramon Botella Method for facilitating pathogen resistance
DE10202419A1 (de) 2002-01-22 2003-08-07 Ribopharma Ag Verfahren zur Hemmung der Expression eines durch eine Chromosomen-Aberration entstandenen Zielgens
EP1572902B1 (en) * 2002-02-01 2014-06-11 Life Technologies Corporation HIGH POTENCY siRNAS FOR REDUCING THE EXPRESSION OF TARGET GENES
CA2474910A1 (en) 2002-02-01 2003-08-07 Sequitur, Inc. Oligonucleotide compositions with enhanced efficiency
US20060009409A1 (en) 2002-02-01 2006-01-12 Woolf Tod M Double-stranded oligonucleotides
AU2003216255A1 (en) * 2002-02-20 2003-09-09 Ribozyme Pharmaceuticals, Inc. RNA INTERFERENCE MEDIATED INHIBITION OF MDR P-GLYCOPROTEIN GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
AU2003211058A1 (en) * 2002-02-20 2003-09-09 Sirna Therapeutics, Inc. RNA INTERFERENCE MEDIATED TARGET DISCOVERY AND TARGET VALIDATION USING SHORT INTERFERING NUCLEIC ACID (siNA)
US7667029B2 (en) 2002-02-20 2010-02-23 Sirna Therapeutics, Inc. RNA interference mediated inhibition of checkpoint kinase-1 (CHK-1) gene expression using short interfering nucleic acid (siNA)
EP1476459A4 (en) * 2002-02-20 2005-05-25 Sirna Therapeutics Inc INHIBITION OF EXPRESSION OF THE CHROMOSOME TRANSLOCATION GENE AGENT BY RNA INTERFERENCE USING SHORT INTERFERING NUCLEIC ACID (siNA)
US9181551B2 (en) 2002-02-20 2015-11-10 Sirna Therapeutics, Inc. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA)
US9657294B2 (en) 2002-02-20 2017-05-23 Sirna Therapeutics, Inc. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA)
AU2003213054A1 (en) * 2002-02-20 2003-09-09 Sirna Therapeutics, Inc. RNA INTERFERENCE MEDIATED INHIBITION OF POLYCOMB GROUP PROTEIN EZH2 GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
EP1432724A4 (en) 2002-02-20 2006-02-01 Sirna Therapeutics Inc RNA inhibition mediated inhibition of MAP KINASE GENES
US20040180438A1 (en) 2002-04-26 2004-09-16 Pachuk Catherine J. Methods and compositions for silencing genes without inducing toxicity
AU2003239851A1 (en) * 2002-05-08 2003-11-11 Xantos Biomedicine Ag Expression constructs for producing double-stranded (ds) rna and the use thereof
WO2003100094A2 (en) * 2002-05-23 2003-12-04 Devgen Nv Method for determining the influence of a compound on cholesterol transport
AU2003243094B2 (en) * 2002-06-21 2007-08-30 Sinogenomax Company Ltd. Randomised DNA libraries and double-stranded RNA libraries, use and method of production thereof
BR0312580A (pt) * 2002-07-10 2006-10-10 Univ Kansas State composições e métodos para controlar nematódeos parasitas
US7655790B2 (en) 2002-07-12 2010-02-02 Sirna Therapeutics, Inc. Deprotection and purification of oligonucleotides and their derivatives
DK1527176T4 (en) 2002-08-05 2017-07-03 Silence Therapeutics Gmbh ADDITIONAL NEW FORMS OF INTERFERRING RNA MOLECULES
US8729036B2 (en) 2002-08-07 2014-05-20 University Of Massachusetts Compositions for RNA interference and methods of use thereof
CA2497892A1 (en) * 2002-09-04 2004-03-18 Provost, Fellows And Scholars Of The College Of The Holy And Undivided T Rinity Of Queen Elizabeth Near Dublin Compositions and methods for tissue specific or inducible inhibition of gene expression
US7923547B2 (en) 2002-09-05 2011-04-12 Sirna Therapeutics, Inc. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA)
CN1774511B (zh) 2002-11-27 2013-08-21 斯昆诺有限公司 用于序列变异检测和发现的基于断裂的方法和系统
WO2004056982A2 (en) * 2002-12-23 2004-07-08 Devgen Nv Kinase sequences
EP1622572B1 (en) 2003-04-30 2017-12-20 Sirna Therapeutics, Inc. Conjugates and compositions for cellular delivery
IL155783A (en) 2003-05-05 2010-11-30 Technion Res & Dev Foundation Multicellular systems of multi-potential embryonic human stem cells and cancer cells and their use
US7619068B2 (en) 2003-05-09 2009-11-17 Diadexus, Inc. Ovr110 antibody compositions and methods of use
US20070092910A1 (en) * 2003-06-17 2007-04-26 Devgen Nv Alcohol dehydrogenase sequences useful for developing compounds for the prevention and/or treatment of metabolic diseases
US9394565B2 (en) 2003-09-05 2016-07-19 Agena Bioscience, Inc. Allele-specific sequence variation analysis
US20060272049A1 (en) * 2003-11-17 2006-11-30 Waterhouse Peter M Insect resistance using inhibition of gene expression
CN102989009B (zh) 2003-12-31 2015-06-03 宾夕法尼亚州研究基金会 预测并克服对卵巢癌化疗的抗性的方法及预测结肠癌发生的方法
ATE452188T1 (de) 2004-02-10 2010-01-15 Sirna Therapeutics Inc Rna-interferenz-vermittelte hemmung der genexpression unter verwendung multifunktioneller sina (short interfering nucleic acid)
WO2005078848A2 (en) 2004-02-11 2005-08-25 University Of Tennessee Research Foundation Inhibition of tumor growth and invasion by anti-matrix metalloproteinase dnazymes
US7622301B2 (en) * 2004-02-24 2009-11-24 Basf Plant Science Gmbh Compositions and methods using RNA interference for control of nematodes
WO2005098050A2 (en) 2004-03-26 2005-10-20 Sequenom, Inc. Base specific cleavage of methylation-specific amplification products in combination with mass analysis
US7608394B2 (en) * 2004-03-26 2009-10-27 Sequenom, Inc. Methods and compositions for phenotype identification based on nucleic acid methylation
CA2562038C (en) 2004-04-02 2017-04-25 The Regents Of The University Of California Methods and compositions for treating and preventing disease associated with .alpha.v.beta.5 integrin
PL1732379T3 (pl) 2004-04-09 2014-04-30 Monsanto Technology Llc Kompozycje i sposoby do zwalczania inwazji szkodników u roślin
WO2005105157A2 (en) 2004-04-23 2005-11-10 The Trustees Of Columbia University In The City Ofnew York INHIBITION OF HAIRLESS PROTEIN mRNA
US10508277B2 (en) 2004-05-24 2019-12-17 Sirna Therapeutics, Inc. Chemically modified multifunctional short interfering nucleic acid molecules that mediate RNA interference
ATE501252T1 (de) 2004-06-22 2011-03-15 Univ Illinois Verfahren zur inhibierung von tumorzellwachstum mit foxm1 sirns
US7968762B2 (en) 2004-07-13 2011-06-28 Van Andel Research Institute Immune-compromised transgenic mice expressing human hepatocyte growth factor (hHGF)
EP2484780A1 (en) 2004-07-23 2012-08-08 The University of North Carolina At Chapel Hill Methods and materials for determining pain sensibility and predicting and treating related disorders
EP1786905B1 (en) 2004-08-18 2011-08-03 Lorus Therapeutics Inc. Small interfering rna molecules against ribonucleotide reductase and uses thereof
EP1799028B1 (en) 2004-09-24 2015-03-04 J.R. Simplot Company Gene silencing
US20060247197A1 (en) 2004-10-04 2006-11-02 Van De Craen Marc Method for down-regulating gene expression in fungi
MX2007004310A (es) * 2004-10-13 2007-06-18 Univ Georgia Res Found Plantas transgenicas resistentes a nematodos.
EP2336333A1 (en) 2004-10-21 2011-06-22 Venganza Inc. Methods and materials for conferring resistance to pests and pathogens of plants
EP1807520B1 (en) 2004-10-25 2012-07-25 Devgen NV Rna constructs
US8772254B2 (en) 2004-10-25 2014-07-08 Devgen N.V. Method and constructs for delivering double stranded RNA to pest organisms
ES2343746T3 (es) 2005-01-07 2010-08-09 Diadexus, Inc. Composiciones de anticuerpo ovr110 y metodos de uso.
US8088976B2 (en) * 2005-02-24 2012-01-03 Monsanto Technology Llc Methods for genetic control of plant pest infestation and compositions thereof
DE202005004135U1 (de) * 2005-03-11 2005-05-19 Klocke Verpackungs-Service Gmbh Mehrkomponentenverpackung mit Applikator
EP2360249A1 (en) 2005-03-31 2011-08-24 Calando Pharmaceuticals, Inc. Inhibitors of ribonucleotide reductase subunit 2 and uses thereof
JP2008540571A (ja) 2005-05-12 2008-11-20 ウィスコンシン・アルムニ・リサーチ・ファウンデーション Pin1の遮断は活性化した免疫細胞によるサイトカイン産生を防ぐ
WO2006129204A2 (en) * 2005-05-31 2006-12-07 Devgen Nv Rnai for control of insects and arachnids
WO2007011702A2 (en) 2005-07-15 2007-01-25 The University Of North Carolina At Chapel Hill Use of egfr inhibitors to prevent or treat obesity
EP2439279B1 (en) 2005-09-16 2016-11-09 Monsanto Technology LLC Methods for genetic control of insect infestations in plants and compositions thereof
EP2295584B1 (en) 2005-09-16 2015-06-10 deVGen N.V. Transgenic plant-based methods for plant pests using RNAi
MX348513B (es) 2005-09-16 2017-06-16 Devgen Nv Metodos para controlar plagas utilizando arni.
AU2006298844B2 (en) 2005-09-20 2012-01-12 Basf Plant Science Gmbh Methods for controlling gene expression using ta-siRAN
US9286469B2 (en) * 2005-12-16 2016-03-15 Cisco Technology, Inc. Methods and apparatus providing computer and network security utilizing probabilistic signature generation
EP2330202A3 (en) 2006-01-06 2011-09-14 University Of Georgia Research Foundation, Inc. Cyst nematode resistant transgenic plants
WO2007080126A2 (en) 2006-01-12 2007-07-19 Devgen N.V. Dsrna as insect control agent
US8906876B2 (en) 2006-01-12 2014-12-09 Devgen Nv Methods for controlling pests using RNAi
EP1971688B1 (en) 2006-01-12 2012-03-14 Devgen NV Dsrna as insect control agent
US20080022423A1 (en) * 2006-02-03 2008-01-24 Monsanto Technology Llc IN PLANTA RNAi CONTROL OF FUNGI
PL2044109T3 (pl) 2006-02-10 2014-11-28 Monsanto Technology Llc Identyfikacja i zastosowanie genów docelowych do zwalczania nicieni pasożytów roślin
CN101384721A (zh) 2006-02-13 2009-03-11 孟山都技术有限公司 选择和稳定dsRNA构建体
WO2007104570A2 (en) * 2006-03-16 2007-09-20 Devgen N.V. Nematode control
US8968702B2 (en) 2006-03-30 2015-03-03 Duke University Inhibition of HIF-1 activation for anti-tumor and anti-inflammatory responses
PL216037B1 (pl) * 2006-06-09 2014-02-28 Inst Biotechnologii I Antybiotykow Kaseta ekspresyjna, zastosowanie kasety ekspresyjnej, wektor, komórka gospodarza oraz sposób otrzymywania polipeptydu
ES2479668T3 (es) 2006-07-11 2014-07-24 University Of Medicine And Dentistry Of New Jersey Proteínas de reparación de la membrana celular, ácidos nucleicos que las codifican y métodos de uso asociados
WO2008014426A2 (en) 2006-07-28 2008-01-31 Children's Memorial Hospital Methods of inhibiting tumor cell aggressiveness using the microenvironment of human embryonic stem cells
AU2007325283B2 (en) 2006-11-27 2012-08-30 Diadexus, Inc. Ovr110 antibody compositions and methods of use
CN101195821A (zh) * 2006-12-04 2008-06-11 中国科学院上海生命科学研究院 利用RNAi技术改良植物抗虫性的方法
WO2008094370A2 (en) 2006-12-22 2008-08-07 University Of Utah Research Foundation Method of detecting ocular diseases and pathologic conditions and treatment of same
US8455188B2 (en) 2007-01-26 2013-06-04 University Of Louisville Research Foundation, Inc. Modification of exosomal components for use as a vaccine
US20080184391A1 (en) * 2007-01-29 2008-07-31 Kuppuswamy Subramaniam Pathogen resistant transgenic plants, associated nucleic acids and techniques involving the same
WO2008103643A1 (en) 2007-02-20 2008-08-28 Monsanto Technology, Llc Invertebrate micrornas
HUE027018T2 (en) 2007-03-21 2016-08-29 Brookhaven Science Ass Llc Combination hairpin antisense compositions and methods for modulating expression
WO2009014565A2 (en) 2007-04-26 2009-01-29 Ludwig Institute For Cancer Research, Ltd. Methods for diagnosing and treating astrocytomas
EP2607477B1 (en) 2007-05-03 2020-09-23 The Brigham and Women's Hospital, Inc. Multipotent stem cells and uses thereof
US8097422B2 (en) 2007-06-20 2012-01-17 Salk Institute For Biological Studies Kir channel modulators
EP2173901A4 (en) * 2007-06-29 2011-12-14 Boston Biomedical Inc DNA MODULATION INDUCED BY MICRO-RNA BACTERIA
US9689031B2 (en) 2007-07-14 2017-06-27 Ionian Technologies, Inc. Nicking and extension amplification reaction for the exponential amplification of nucleic acids
WO2009012263A2 (en) 2007-07-18 2009-01-22 The Trustees Of Columbia University In The City Of New York Tissue-specific micrornas and compositions and uses thereof
ES2651911T3 (es) 2007-08-14 2018-01-30 Commonwealth Scientific And Industrial Research Organisation Métodos mejorados de silenciamiento génico
KR101142209B1 (ko) 2007-09-22 2012-05-04 재단법인서울대학교산학협력재단 섭취 RNAi를 이용한 꼬마선충에서 두 유전자의동시발현 억제방법
US7968525B1 (en) 2007-12-03 2011-06-28 University Of Florida Research Foundation, Inc. Use of RNA interference to validate new termiticide target sites and a method of termite control
EP2283133A2 (en) 2008-04-04 2011-02-16 Calando Pharmaceuticals, Inc. Compositions and use of epas1 inhibitors
WO2009126896A2 (en) 2008-04-10 2009-10-15 Monsanto Technology Llc Methods and compositions for root knot nematode control
GB0807018D0 (en) 2008-04-17 2008-05-21 Fusion Antibodies Ltd Antibodies and treatment
WO2010054221A2 (en) 2008-11-06 2010-05-14 The Johns Hopkins University Treatment of chronic inflammatory respiratory disorders
WO2010054379A2 (en) 2008-11-10 2010-05-14 The United States Of America, As Represensted By The Secretary, Department Of Health And Human Services Gene signature for predicting prognosis of patients with solid tumors
EP2379722B1 (de) 2008-12-16 2016-09-07 c-LEcta GmbH Expressionsvektor
JP2012513464A (ja) 2008-12-23 2012-06-14 ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク ホスホジエステラーゼ阻害剤及びその使用
WO2010074783A1 (en) 2008-12-23 2010-07-01 The Trustees Of Columbia University In The City Of New York Phosphodiesterase inhibitors and uses thereof
JP2012520685A (ja) 2009-03-19 2012-09-10 メルク・シャープ・エンド・ドーム・コーポレイション 低分子干渉核酸(siNA)を用いたGATA結合タンパク質3(GATA3)遺伝子発現のRNA干渉媒介性阻害
US20120035247A1 (en) 2009-03-19 2012-02-09 Merck Sharp & Dohme Corp. RNA Interference Mediated Inhibition of Signal Transducer and Activator of Transcription 6 (STAT6) Gene Expression Using Short Interfering Nucleic Acid (siNA)
EA201171144A1 (ru) 2009-03-19 2012-04-30 Мерк Шарп Энд Домэ Корп. ОПОСРЕДОВАННОЕ РНК-ИНТЕРФЕРЕНЦИЕЙ ИНГИБИРОВАНИЕ ЭКСПРЕССИИ ГЕНА ГОМОЛОГА 1 BTB И CNC, ОСНОВНОГО ФАКТОРА ТРАНСКРИПЦИИ С ЛЕЙЦИНОВОЙ МОЛНИЕЙ 1 (Bach1) С ИСПОЛЬЗОВАНИЕМ МАЛОЙ ИНТЕРФЕРИРУЮЩЕЙ НУКЛЕИНОВОЙ КИСЛОТЫ (миНК)
US20120016011A1 (en) 2009-03-19 2012-01-19 Merck Sharp & Dohme Corp. RNA Interference Mediated Inhibition of Connective Tissue Growth Factor (CTGF) Gene Expression Using Short Interfering Nucleic Acid (siNA)
JP2012521762A (ja) 2009-03-27 2012-09-20 メルク・シャープ・エンド・ドーム・コーポレイション 低分子干渉核酸(siNA)を用いた神経成長因子β鎖(NGFβ)遺伝子発現のRNA干渉媒介性阻害
EP2411516A1 (en) 2009-03-27 2012-02-01 Merck Sharp&Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF APOPTOSIS SIGNAL-REGULATING KINASE 1 (ASK1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
US20120022143A1 (en) 2009-03-27 2012-01-26 Merck Sharp & Dohme Corp RNA Interference Mediated Inhibition of the Thymic Stromal Lymphopoietin (TSLP) Gene Expression Using Short Interfering Nucliec Acid (siNA)
WO2010111497A2 (en) 2009-03-27 2010-09-30 Merck Sharp & Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF THE INTERCELLULAR ADHESION MOLECULE 1 (ICAM-1)GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
WO2010111471A2 (en) 2009-03-27 2010-09-30 Merck Sharp & Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 (STAT1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
US20100257634A1 (en) * 2009-04-03 2010-10-07 Venganza Inc. Bioassay for gene silencing constructs
US8283332B2 (en) 2009-04-17 2012-10-09 University Of Louisville Research Foundation, Inc. PFKFB4 inhibitors and methods of using the same
EP2258858A1 (en) 2009-06-05 2010-12-08 Universitätsklinikum Freiburg Transgenic LSD1 animal model for cancer
EP2453923B1 (en) 2009-07-14 2015-11-11 Mayo Foundation For Medical Education And Research Peptide-mediated non-covalent delivery of active agents across the blood brain barrier
KR101752515B1 (ko) 2009-07-24 2017-06-29 더 리젠츠 오브 더 유니버시티 오브 캘리포니아 Avb5 인테그린과 결부된 질환의 치료 및 예방을 위한 방법 및 조성물
BR122018067960B8 (pt) 2009-08-28 2022-12-06 Du Pont Polinucleotídeo isolado, cassete de expressão, método para controlar uma praga de plantas do tipo coleoptera e método para obtenção de uma planta
US9163240B2 (en) 2009-12-07 2015-10-20 The Johns Hopkins University SR-BI mutation as a predictor of low progesterone levels and poor fetal viability during pregnancy
CN102741410B (zh) 2009-12-09 2016-11-16 日东电工株式会社 Hsp47表达的调节
WO2011072243A1 (en) 2009-12-10 2011-06-16 The Trustees Of Columbia University In The City Of New York Histone acetyltransferase activators and uses thereof
US10640457B2 (en) 2009-12-10 2020-05-05 The Trustees Of Columbia University In The City Of New York Histone acetyltransferase activators and uses thereof
MX369004B (es) 2009-12-18 2019-10-24 Novartis Ag Composiciones orgánicas para tratar las enfermedades relacionadas con hsf1.
CN102905763B (zh) 2009-12-23 2015-06-17 诺华股份有限公司 脂质、脂质组合物和使用它们的方法
MX344543B (es) 2010-01-26 2016-12-19 Nat Jewish Health Metodos y composiciones para prediccion de riesgo, diagnosis, prognosis y tratamiento de desordenes pulmonares.
AU2011214465A1 (en) 2010-02-10 2012-08-30 Novartis Ag Methods and compounds for muscle growth
CA2800065A1 (en) 2010-05-21 2011-11-24 Peptimed, Inc. Reagents and methods for treating cancer
GB201009601D0 (en) 2010-06-08 2010-07-21 Devgen Private Ltd Method for down-grading gene expression in fungi
US9168297B2 (en) 2010-06-23 2015-10-27 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Regulation of skin pigmentation by neuregulin-1 (NRG-1)
EP3330377A1 (en) 2010-08-02 2018-06-06 Sirna Therapeutics, Inc. Rna interference mediated inhibition of catenin (cadherin-associated protein), beta 1 (ctnnb1) gene expression using short interfering nucleic acid (sina)
EP3587574B1 (en) 2010-08-17 2022-03-16 Sirna Therapeutics, Inc. Rna interference mediated inhibition of hepatitis b virus (hbv) gene expression using short interfering nucleic acid (sina)
CN103140582A (zh) 2010-08-24 2013-06-05 默沙东公司 含有内部非核酸间隔子的单链RNAi试剂
WO2012027467A1 (en) 2010-08-26 2012-03-01 Merck Sharp & Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF PROLYL HYDROXYLASE DOMAIN 2 (PHD2) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
US20140134231A1 (en) 2010-10-11 2014-05-15 Sanford-Burnham Medical Research Institute Mir-211 expression and related pathways in human melanoma
CN108404115A (zh) 2010-10-15 2018-08-17 纽约市哥伦比亚大学理事会 肥胖症-相关的基因和它们的蛋白和其用途
EP3327125B1 (en) 2010-10-29 2020-08-05 Sirna Therapeutics, Inc. Rna interference mediated inhibition of gene expression using short interfering nucleic acids (sina)
AU2011323508B2 (en) 2010-11-01 2017-04-27 Peptimed, Inc. Compositions of a peptide targeting system for treating cancer
WO2013149194A1 (en) 2012-03-29 2013-10-03 The Trustees Of Columbia University In The City Of New York Methods for treating hair loss disorders
EP2635299B1 (en) 2010-11-02 2019-07-31 The Trustees of Columbia University in the City of New York Methods for treating hair loss disorders
US9198911B2 (en) 2010-11-02 2015-12-01 The Trustees Of Columbia University In The City Of New York Methods for treating hair loss disorders
CN103298939A (zh) 2010-12-06 2013-09-11 夸克医药公司 包含位置修饰的双链寡核苷酸化合物
US9150926B2 (en) 2010-12-06 2015-10-06 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Diagnosis and treatment of adrenocortical tumors using human microRNA-483
JP6616057B2 (ja) 2010-12-22 2019-12-04 ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク ヒストンアセチル基転移酵素モジュレーターおよびその使用
US9205100B2 (en) 2011-03-03 2015-12-08 Quark Pharmaceuticals, Inc. Compositions and methods for treating lung disease and injury
US10196637B2 (en) 2011-06-08 2019-02-05 Nitto Denko Corporation Retinoid-lipid drug carrier
TWI658830B (zh) 2011-06-08 2019-05-11 日東電工股份有限公司 Hsp47表現調控強化用類視色素脂質體
AU2012301617A1 (en) 2011-09-02 2014-04-17 Salk Institute For Biological Studies CaMKII, IP3R, calcineurin, p38 and MK2/3 inhibitors to treat metabolic disturbances of obesity
US9352312B2 (en) 2011-09-23 2016-05-31 Alere Switzerland Gmbh System and apparatus for reactions
LT2766393T (lt) 2011-10-14 2018-10-10 F. Hoffmann-La Roche Ag Antikūnai prieš htra1 ir jų naudojimo būdai
EP3597644B1 (en) 2011-10-18 2021-09-29 Dicerna Pharmaceuticals, Inc. Amine cationic lipids and uses thereof
BR112014010769B1 (pt) 2011-11-03 2021-08-03 Quark Pharmaceuticals, Inc Uso de um composto de rna de fita dupla para preparar um medicamento para tratar doença de ménière
WO2013158966A1 (en) 2012-04-20 2013-10-24 Futuragene Israel Ltd. Bronze bug control agents
WO2013163085A2 (en) 2012-04-23 2013-10-31 Futuragene Israel Ltd. Glycaspis brimblecombei control agents
WO2013165816A2 (en) 2012-05-02 2013-11-07 Merck Sharp & Dohme Corp. SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
ES2817897T3 (es) 2012-07-23 2021-04-08 La Jolla Inst Allergy & Immunology PTPRS y proteoglicanos en enfermedad autoinmune
BR112015007123A2 (pt) 2012-10-03 2017-08-08 Futuragene Israel Ltd molécula de ácido ribonucléico de filamento duplo (dsrna) isolada, vetor, célula hospedeira, tecido vegetal, ácido nucléico isolado, e, métodos para produzir uma planta resistente a uma praga e para inibir uma infestação de praga
EP3677310A1 (en) 2012-10-08 2020-07-08 St. Jude Children's Research Hospital Therapies based on control of regulatory t cell stability and function via a neuropilin-1:semaphorin axis
US9920316B2 (en) 2013-03-14 2018-03-20 Pioneer Hi-Bred International, Inc. Compositions and methods to control insect pests
KR20150129847A (ko) 2013-03-15 2015-11-20 더 트러스티스 오브 컬럼비아 유니버시티 인 더 시티 오브 뉴욕 융합 단백질 및 이들의 방법
EP2810952A1 (en) 2013-06-03 2014-12-10 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Novel pest control methods
EP3016716B1 (en) 2013-07-03 2020-06-17 City of Hope Anticancer combination of a bacterial cell and a tumor penetrating agent
US10584387B2 (en) 2013-10-09 2020-03-10 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Detection of hepatitis delta virus (HDV) for the diagnosis and treatment of Sjögren's syndrome and lymphoma
WO2015070158A1 (en) 2013-11-11 2015-05-14 Sirna Therapeutics, Inc. Systemic delivery of myostatin short interfering nucleic acids (sina) conjugated to a lipophilic moiety
US9682123B2 (en) 2013-12-20 2017-06-20 The Trustees Of Columbia University In The City Of New York Methods of treating metabolic disease
JP6372930B2 (ja) 2013-12-27 2018-08-15 国立大学法人高知大学 悪性腫瘍の治療薬
EP3169309B1 (en) 2014-07-16 2023-05-10 Novartis AG Method of encapsulating a nucleic acid in a lipid nanoparticle host
WO2016059187A1 (en) * 2014-10-16 2016-04-21 Universite De Strasbourg Method of capturing and identifying novel rnas
WO2016077624A1 (en) 2014-11-12 2016-05-19 Nmc, Inc. Transgenic plants with engineered redox sensitive modulation of photosynthetic antenna complex pigments and methods for making the same
EP3237452A4 (en) 2014-12-23 2018-12-05 The Trustees of Columbia University in the City of New York Fusion proteins and methods thereof
US10264976B2 (en) 2014-12-26 2019-04-23 The University Of Akron Biocompatible flavonoid compounds for organelle and cell imaging
WO2016145003A1 (en) 2015-03-09 2016-09-15 University Of Kentucky Research Foundation Rna nanoparticle for treatment of gastric cancer
CN111961103B (zh) 2015-03-09 2023-06-16 肯塔基大学研究基金会 用于脑肿瘤治疗的rna纳米颗粒
US11085044B2 (en) 2015-03-09 2021-08-10 University Of Kentucky Research Foundation miRNA for treatment of breast cancer
US11279768B1 (en) 2015-04-03 2022-03-22 Precision Biologics, Inc. Anti-cancer antibodies, combination therapies, and uses thereof
US10828381B2 (en) 2015-04-17 2020-11-10 University Of Kentucky Research Foundation RNA nanoparticles and method of use thereof
US20180156807A1 (en) 2015-04-29 2018-06-07 New York University Method for treating high-grade gliomas
WO2016210292A1 (en) 2015-06-25 2016-12-29 Children's Medical Center Corporation Methods and compositions relating to hematopoietic stem cell expansion, enrichment, and maintenance
US10072065B2 (en) 2015-08-24 2018-09-11 Mayo Foundation For Medical Education And Research Peptide-mediated delivery of immunoglobulins across the blood-brain barrier
EP3702470A3 (en) 2015-09-09 2020-10-07 The Trustees of Columbia University in the City of New York Reduction of er-mam-localized app-c99 and methods of treating alzheimer's disease
US11285142B2 (en) 2015-09-29 2022-03-29 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Compositions and methods for identifying and treating dystonia disorders
CA3088612C (en) 2015-10-30 2022-04-12 Genentech, Inc. Anti-htra1 antibodies and methods of use thereof
KR20180086260A (ko) 2015-12-13 2018-07-30 닛토덴코 가부시키가이샤 높은 활성 및 감소한 오프 타겟을 위한 sirna 구조
EP3423568A4 (en) 2016-03-04 2019-11-13 University Of Louisville Research Foundation, Inc. METHOD AND COMPOSITIONS FOR EX-VIVO REPRODUCTION OF VERY SMALL EMBRYONAL STEM CELLS (VSELS)
DK3429603T3 (da) 2016-03-15 2022-03-14 Childrens Medical Center Fremgangsmåder og sammensætninger vedrørende ekspansion af hæmatopoietiske stamceller
WO2017173327A1 (en) 2016-03-31 2017-10-05 The Schepens Eye Research Institute, Inc. Endomucin inhibitor as an anti-angiogenic agent
WO2018057575A1 (en) 2016-09-21 2018-03-29 Alnylam Pharmaceuticals, Inc Myostatin irna compositions and methods of use thereof
US20210162007A1 (en) 2018-04-09 2021-06-03 President And Fellows Of Harvard College Modulating nuclear receptors and methods of using same
CN109266677B (zh) * 2018-08-31 2021-11-23 中国烟草总公司郑州烟草研究院 一种全长转录因子酵母双杂交文库的构建方法
CN109183158B (zh) * 2018-08-31 2021-11-23 中国烟草总公司郑州烟草研究院 一种全长转录因子酵母单杂交文库的构建方法
CN113015746A (zh) 2018-09-19 2021-06-22 拉荷亚免疫研究所 在类风湿性关节炎中的ptprs和蛋白聚糖
PT3880212T (pt) 2018-11-16 2024-02-08 Nitto Denko Corp Formulação e métodos de administração de rna de interferência para tumores malignos
JP7317379B2 (ja) * 2019-01-04 2023-07-31 国立大学法人京都大学 潰瘍性大腸炎及び原発性硬化性胆管炎の検査方法
CN110229839B (zh) * 2019-06-04 2021-06-08 中国农业大学 一种提升大肠杆菌dsRNA表达产率的方法
EP3825408A1 (en) 2019-11-19 2021-05-26 FRAUNHOFER-GESELLSCHAFT zur Förderung der angewandten Forschung e.V. Methods of multi-species insect pest control
IL293530A (en) 2019-12-18 2022-08-01 Novartis Ag Derivatives of 3-(5-methoxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione and their uses
WO2021123920A1 (en) 2019-12-18 2021-06-24 Novartis Ag Compositions and methods for the treatment of hemoglobinopathies
EP4087652A1 (en) 2020-01-08 2022-11-16 Regeneron Pharmaceuticals, Inc. Treatment of fibrodysplasia ossificans progressiva
WO2021150300A1 (en) 2020-01-22 2021-07-29 Massachusetts Institute Of Technology Inducible tissue constructs and uses thereof
WO2021173965A1 (en) 2020-02-28 2021-09-02 Massachusetts Institute Of Technology Identification of variable influenza residues and uses thereof
CN113638055B (zh) * 2020-05-22 2023-07-07 江苏省疾病预防控制中心(江苏省公共卫生研究院) 一种制备双链rna测序文库的方法
WO2022147481A1 (en) 2020-12-30 2022-07-07 Ansun Biopharma Inc. Combination therapy of an oncolytic virus delivering a foreign antigen and an engineered immune cell expressing a chimeric receptor targeting the foreign antigen
EP4359527A2 (en) 2021-06-23 2024-05-01 Novartis AG Compositions and methods for the treatment of hemoglobinopathies
WO2023012165A1 (en) 2021-08-02 2023-02-09 Universite De Montpellier Compositions and methods for treating cmt1a or cmt1e diseases with rnai molecules targeting pmp22
CN113533007B (zh) * 2021-08-06 2023-11-24 青岛瑞斯凯尔生物科技有限公司 一种抗体染色标记装置及其方法
WO2023064928A2 (en) 2021-10-14 2023-04-20 Arsenal Biosciences, Inc. Immune cells having co-expressed shrnas and logic gate systems
TW202417626A (zh) 2022-09-13 2024-05-01 美商亞森諾生物科學公司 具有共表現的tgfbr shrna之免疫細胞
WO2024059824A2 (en) 2022-09-16 2024-03-21 Arsenal Biosciences, Inc. Immune cells with combination gene perturbations

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US589801A (en) * 1897-09-07 woltereck
EP1213348A2 (en) 1985-03-21 2002-06-12 Johnston, Stephen, Ph.D. Parasite-derived resistance
US6608241B1 (en) 1985-10-29 2003-08-19 Monsanto Technology Llc Protection of plants against viral infection
NZ219472A (en) 1986-03-28 1990-08-28 Calgene Inc Regulation of phenotype in plant cells using dsdna constructs
US5017488A (en) * 1986-04-01 1991-05-21 University Of Medicine And Dentistry Of New Jersey Highly efficient dual T7/T3 promoter vector PJKF16 and dual SP6/T3 promoter vector PJFK15
US4970168A (en) * 1989-01-27 1990-11-13 Monsanto Company Virus-resistant plants
WO1990014090A1 (en) * 1989-05-19 1990-11-29 Hem Research, Inc. SHORT THERAPEUTIC dsRNA OF DEFINED STRUCTURE
HUT57265A (en) 1989-11-03 1991-11-28 Zaadunie Bv Process for producing plants of diminished infection-sensitivity
US5837848A (en) * 1990-03-16 1998-11-17 Zeneca Limited Root-specific promoter
JPH05505727A (ja) * 1990-03-30 1993-08-26 プレジデント、アンド、フェローズ、オブ、ハーバード、カレッジ トランスジェニック動物においてトランス遺伝子の発現をコントロールするバイナリー遺伝子系
US5831011A (en) * 1990-07-27 1998-11-03 Mycogen Corporation Bacillus thuringiensis genes encoding nematode-active toxins
US5459252A (en) * 1991-01-31 1995-10-17 North Carolina State University Root specific gene promoter
WO1993019188A1 (en) 1992-03-20 1993-09-30 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Fungus-responsive chimaeric gene
DE4234131C2 (de) * 1992-10-09 1995-08-24 Max Planck Gesellschaft Transgener pathogen-resistenter Organismus
CA2088379A1 (en) * 1993-01-29 1994-07-30 University Of British Columbia Biological systems incorporating stress-inducible genes and reporter constructs for environmental biomonitoring and toxicology
IL104830A (en) * 1993-02-23 2001-01-28 Yissum Res Dev Co A chimeric plasmid containing a non-structural gene for the protease of the potato virus and its various uses
DE4317845A1 (de) * 1993-05-28 1994-12-01 Bayer Ag Desoxyribonukleinsäuren
WO1995034680A1 (en) * 1994-06-15 1995-12-21 The Trustees Of Columbia University In The City Of New York Method to identify tumor suppressor genes
US5691140A (en) * 1995-05-18 1997-11-25 New England Biolabs, Inc. Bidirectional in vitro transcription vectors utilizing a single RNA polymerase for both directions
GB9510944D0 (en) * 1995-05-31 1995-07-26 Bogaert Thierry Assays and processes for the identification of compounds which control cell behaviour,the compounds identified and their use in the control of cell behaviour
WO1996038553A1 (en) * 1995-06-02 1996-12-05 M&E Biotech A/S A method for identification of biologically active peptides and nucleic acids
US5679551A (en) * 1995-10-31 1997-10-21 Board Of Regents, The University Of Texas System Unique double-stranded RNAS associated with the Trichomonas vaginalis virus
US5898031A (en) * 1996-06-06 1999-04-27 Isis Pharmaceuticals, Inc. Oligoribonucleotides for cleaving RNA
DE19631919C2 (de) * 1996-08-07 1998-07-16 Deutsches Krebsforsch Anti-Sinn-RNA mit Sekundärstruktur
PL191777B1 (pl) * 1996-08-09 2006-07-31 Keygene Nv Izolowany kwas nukleinowy, rekombinowany konstrukt DNA, wektor, plazmid, komórka bakterii, rekombinowany genom rośliny, komórki roślinne, roślina, nasiona transgeniczne, sposób otrzymywania roślin, sposób zabezpieczania roślin, sposób izolowania kwasu nukleinowego, sposób identyfikacji kwasu nukleinowego, kombinacja primerów, zestaw diagnostyczny, sposób detekcji, polipeptyd i RNA
JP2001503972A (ja) * 1996-09-18 2001-03-27 ユング,クリスチャン 線虫抵抗性遺伝子
JP4073960B2 (ja) 1996-10-03 2008-04-09 肇 加藤 炭化水素の水蒸気改質方法
DE69704960T2 (de) 1996-12-18 2002-03-28 Exxonmobil Chemical Patents Inc., Baytown Kompatibilisierte polymermischungen hergestellt unter verwendung eines multifunktionellen mittels
GB9703146D0 (en) 1997-02-14 1997-04-02 Innes John Centre Innov Ltd Methods and means for gene silencing in transgenic plants
US6506559B1 (en) * 1997-12-23 2003-01-14 Carnegie Institute Of Washington Genetic inhibition by double-stranded RNA
AUPP249298A0 (en) * 1998-03-20 1998-04-23 Ag-Gene Australia Limited Synthetic genes and genetic constructs comprising same I
JP5015373B2 (ja) * 1998-04-08 2012-08-29 コモンウェルス サイエンティフィック アンド インダストリアル リサーチ オーガニゼイション 改良表現型を得るための方法及び手段
AR020078A1 (es) * 1998-05-26 2002-04-10 Syngenta Participations Ag Metodo para alterar la expresion de un gen objetivo en una celula de planta
GB9827152D0 (en) 1998-07-03 1999-02-03 Devgen Nv Characterisation of gene function using double stranded rna inhibition
GB9814536D0 (en) 1998-07-03 1998-09-02 Devgen Nv Characterisation of gene function using double stranded rna inhibition
AUPR621501A0 (en) 2001-07-06 2001-08-02 Commonwealth Scientific And Industrial Research Organisation Delivery of ds rna
EP2439279B1 (en) 2005-09-16 2016-11-09 Monsanto Technology LLC Methods for genetic control of insect infestations in plants and compositions thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107858405A (zh) * 2017-10-12 2018-03-30 华南农业大学 一种测定外源dsRNA对瓢虫毒性影响的方法
CN110746497A (zh) * 2019-11-18 2020-02-04 维塔恩(广州)医药有限公司 肺炎衣原体相关抗原短肽及其应用
CN110804088A (zh) * 2019-11-18 2020-02-18 维塔恩(广州)医药有限公司 巨细胞病毒相关抗原短肽及其应用

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