CN113957156B - 一种用精巢特异蛋白基因评价昆虫种群质量的方法 - Google Patents

一种用精巢特异蛋白基因评价昆虫种群质量的方法 Download PDF

Info

Publication number
CN113957156B
CN113957156B CN202111337551.3A CN202111337551A CN113957156B CN 113957156 B CN113957156 B CN 113957156B CN 202111337551 A CN202111337551 A CN 202111337551A CN 113957156 B CN113957156 B CN 113957156B
Authority
CN
China
Prior art keywords
leu
ile
ser
lys
val
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN202111337551.3A
Other languages
English (en)
Other versions
CN113957156A (zh
Inventor
毛建军
刘小平
张礼生
王孟卿
李玉艳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Institute of Plant Protection of Chinese Academy of Agricultural Sciences
Original Assignee
Institute of Plant Protection of Chinese Academy of Agricultural Sciences
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Institute of Plant Protection of Chinese Academy of Agricultural Sciences filed Critical Institute of Plant Protection of Chinese Academy of Agricultural Sciences
Priority to CN202111337551.3A priority Critical patent/CN113957156B/zh
Publication of CN113957156A publication Critical patent/CN113957156A/zh
Application granted granted Critical
Publication of CN113957156B publication Critical patent/CN113957156B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6888Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/43504Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
    • C07K14/43563Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates from insects
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions
    • C12Q1/6851Quantitative amplification
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/124Animal traits, i.e. production traits, including athletic performance or the like
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/158Expression markers
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/166Oligonucleotides used as internal standards, controls or normalisation probes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Wood Science & Technology (AREA)
  • Analytical Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • General Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Insects & Arthropods (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Toxicology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Medicinal Chemistry (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

本发明涉及一种用精巢特异蛋白基因评价昆虫种群质量的方法,包括以下步骤:通过检测精巢特异蛋白基因的表达水平来评价昆虫质量。采用上述方法可以评价雄虫寿命、交配后雌虫繁殖能力等。特别是用于评价经过室内多代饲养后或研制人工饲料时昆虫的繁殖能力。采用本发明的检测方法评价昆虫群体质量仅需1天,而用传统的方法计数昆虫寿命与产卵量来评价昆虫质量,通常需要至少1个月时间。本发明的检测方法涉及的材料易于获得,操作方便、快捷、高效,适合于在昆虫规模化生产中推广应用。

Description

一种用精巢特异蛋白基因评价昆虫种群质量的方法
技术领域
本发明属于农业害虫生物防治技术领域,尤其涉及一种用精巢特异蛋白基因评价昆虫种群质量的方法。
背景技术
利用天敌昆虫防治害虫是一种非常重要的农业害虫防治方法,对于保障农产品质量、保护生态环境具有重大的战略意义。要利用天敌昆虫,首先必须大量生产天敌昆虫。在天敌昆虫生产过程中有一个普遍的问题,就是经过连续多代饲养后,天敌昆虫质量可能下降,主要表现为死亡率升高、寿命缩短、产卵量减少、卵质量下降等。但是,目前在天敌昆虫释放前还缺乏全面而快捷有效的评价整个天敌昆虫种群质量的方法。现有方法都是评价雌虫,不涉及雄虫。这种方法不太全面,也不太科学,因为雌虫的繁殖能力在很大程度上受与之交配的雄虫的影响。雌虫的质量好,但雄虫质量不好,雌虫的繁殖能力仍然不会高。
大草蛉(Chrysopa pallens)是一种非常重要的捕食性天敌昆虫。其能捕食各种蚜虫,鳞翅目害虫的卵与低龄幼虫,粉虱等各种害虫。大草蛉捕食量大,单头幼虫每日可捕食上百头蚜虫,被称为“蚜狮”。大草蛉繁殖能力强,单头雌成虫一生可产卵上千粒,甚至达1500粒。大草蛉分布广,在全世界主要的农林生态系统都有分布。由此可见大草蛉具有非常好的应用前景。大草蛉在规模化饲养过程中,同样可能会出现种群质量下降的情况,包括寿命缩短,雄虫交配能力衰退,雌虫产卵量下降等,质量下降的种群严重影响产品质量与生产效率,并大幅提高生产成本。因此,快捷高效地评价种群质量至关重要。
发明内容
鉴于现有技术所存在的问题,本发明提供一种用精巢特异蛋白基因评价昆虫种群质量的方法,通过检测精巢特异蛋白基因的表达水平,可以评价昆虫种群质量,例如与雄虫寿命、交配后雌虫繁殖能力等,具有方便快捷高效等优点。
本发明解决上述技术问题的技术方案如下:
本发明提供一种精巢特异蛋白基因包括SEQ ID NO:1所示的核苷酸序列。
本发明提供精巢特异蛋白包括SEQ ID NO:2所示的氨基酸序列。
本发明的有益效果包括:本发明提供的精巢特异蛋白基因(tbp)是一个全新的基因,其核苷酸序列与氨基酸序列与以前的精液蛋白基因、附腺蛋白基因等生殖相关基因的序列完全不同。Tbp基因的开放阅读框很长,达到9201bp,编码精巢特异蛋白,是一个大蛋白,分子量达350.064kDa。发明人在研究中意外发现Tbp在雄虫与雌虫生殖中发挥非常重要的功能。精巢特异蛋白基因和/或精巢特异蛋白可以用于评价昆虫种群质量。
本发明提供精巢特异蛋白基因表达水平在评价昆虫种群质量中的应用。
本发明的有益效果包括:发明人在研究中意外发现精巢特异蛋白基因的表达水平与雄虫寿命、产卵总量、交配后雌虫繁殖能力成正相关,通过检测精巢特异蛋白基因的表达水平可以评价昆虫种群质量,具有方便、快捷、高效,适合于在昆虫规模化生产中推广应用等优点。
发明人在研究中意外发现Tbp是雄虫精子发生所必须的,此基因功能缺失会导致精子尾部出现明显缺陷,精子活力显著下降,雄虫寿命显著缩短。同时,tbp的表达也对交配后雌虫的卵子发生具有重大影响。如果雄虫tbp的功能缺失,与野生型雌虫交配后,雌虫的卵子发生受到严重影响,卵巢干细胞分化受到明显抑制,产卵量显著下降,卵重与孵化率显著下降。所以,通过检测tbp基因的表达水平,可以同时评价雄虫与雌虫,甚至后代的质量。本发明的实验证明,通过检测精巢特异蛋白基因的表达水平可以用于评价群体中雄虫寿命及雌虫的繁殖能力,特别是经过室内多代饲养后或研制人工饲料时昆虫的繁殖能力。
在具体应用时,可以用于大草蛉的昆虫种群质量的评价,例如:用于评价产卵总量、寿命、卵重、孵化率等指标。
进一步,精巢特异蛋白基因的核苷酸序列包括SEQ ID NO:1所示的核苷酸序列。
进一步,精巢特异蛋白基因编码的蛋白质的氨基酸序列包括SEQ ID NO:2所示的氨基酸序列。
本发明提供用于检测精巢特异蛋白基因的表达水平的物质在评价昆虫种群质量中的应用。
本发明提供一种用于评价昆虫种群质量的引物,包括用于检测精巢特异蛋白基因的表达水平的引物。
例如:在本发明的实施例中,用于检测精巢特异蛋白基因的表达水平的引物包括包括SEQ ID NO:3所示的核苷酸序列和SEQ ID NO:4所示的核苷酸序列。采用上述引物进行检测时,具有特异性好、扩增效果高等优点。
本发明提供一种用于评价昆虫种群质量的试剂盒,包括上述的引物。采用上述试剂盒可以方便、快捷、高效的评价昆虫种群质量,尤其是评价大草蛉的产卵总量、寿命、卵重、孵化率等指标。
所述试剂盒除了包括上述引物外,还可以包括其他用于荧光定量PCR检测的试剂,例如以下试剂中的一种或几种的组合:水、缓冲液、荧光定量PCR检测所用的酶、镁离子、dNTPs、荧光染料、内参基因引物等。
上述内参基因的引物序列可以包括SEQ ID NO:5所示的核苷酸序列和SEQ ID NO:6所示的核苷酸序列。
本发明提供上述引物和/或上述试剂盒在评价昆虫种群质量中的应用。采用上述引物或试剂盒评价昆虫种群质量具有方便、快捷、高效等优点。
本发明提供一种用精巢特异蛋白基因评价昆虫种群质量的方法,包括以下步骤:检测精巢特异蛋白基因的表达水平。
采用上述方案的有益效果是:采用本发明的方法评价昆虫群体质量仅需1天,而用传统的方法计数昆虫寿命与产卵量,通常需要至少1个月时间。本发明的检测方法涉及的材料易于获得,操作方便、快捷、高效、结果准确,适合于在昆虫规模化生产中推广应用。
进一步,采用实时荧光PCR方法检测精巢特异蛋白基因的表达水平。
进一步,荧光定量PCR方法采用的引物包括SEQ ID NO:3所示的核苷酸序列和SEQID NO:4所示的核苷酸序列。
在具体实施过程中,荧光定量PCR的反应体系可以包括:待检测cDNA模板、检测精巢特异蛋白基因的表达水平的引物、内参基因引物、水、缓冲液、荧光定量PCR用酶、镁离子、dNTPs、荧光染料。在反应体系中还可以包括对照组。
荧光定量PCR的反应条件可以包括:95℃、2min;95℃、10s,60℃、30s,40个循环;95℃、10s,65℃、60s;97℃、1s。
采用上述的反应体系和反应条件,有利于保障引物的特异性,减少非特异性扩增,真实反映基因的表达水平。
用精巢特异蛋白基因评价昆虫种群质量的方法的评价标准包括:调节cDNA浓度,将内参基因的ct值控制在15.5-16.5之间。当ct值之差(tbp基因ct值-内参基因ct值)等于或小于15.73时,说明群体的质量正常;当ct值之差(tbp基因ct值-内参基因ct值)大于15.73时,说明群体的质量下降,差值越大,群体质量越差。
具体的,当ct值之差(tbp基因ct值-内参基因ct值)等于或小于15.73时,说明群体寿命正常;当ct值之差(tbp基因ct值-内参基因ct值)大于15.73时,说明群体寿命下降,差值越大,群体寿命下降越多。
当ct值之差(tbp基因ct值-内参基因ct值)等于或小于15.73时,说明产卵总量正常;当ct值之差(tbp基因ct值-内参基因ct值)大于15.73时,说明产卵总量下降,差值越大,产卵总量下降越多。
当ct值之差(tbp基因ct值-内参基因ct值)等于或小于15.73时,说明群体的卵重正常;当ct值之差(tbp基因ct值-内参基因ct值)大于15.73时,说明卵重下降,差值越大,卵重下降越多。
当ct值之差(tbp基因ct值-内参基因ct值)等于或小于15.73时,说明群体的孵化率正常;当ct值之差(tbp基因ct值-内参基因ct值)大于15.73时,说明孵化率下降,差值越大,孵化率下降越多。
在本发明实施例中,内参基因为actin基因。
附图说明
图1为本发明实施例中扩增雄虫精巢特异蛋白基因tbp与内参基因actin的引物的熔解曲线。
图2为本发明实施例第1代成虫和第20代成虫的tbp的表达水平的检测结果(图中不同的字母表示有显著性差异)。
图3为本发明实施例第1代成虫和第20代成虫的产卵总量的检测结果(图中不同的字母表示有显著性差异)。
图4为本发明实施例第1代成虫和第20代成虫的寿命的检测结果(图中不同的字母表示有显著性差异)。
图5为本发明实施例第1代成虫和第20代成虫的卵重的检测结果(图中不同的字母表示有显著性差异)。
图6为本发明实施例第1代成虫和第20代成虫的卵孵化率检测结果(图中不同的字母表示有显著性差异)。
具体实施方式
以下结合附图对本发明的原理和特征进行描述,所举实例只用于解释本发明,并非用于限定本发明的范围。
本发明提供了一种用精巢特异蛋白基因评价昆虫群体质量的方法,通过检测大草蛉精巢特异蛋白基因的表达水平,预测大草蛉雄虫寿命,及与其交配后雌虫的繁殖能力,从而全面、快捷、高效、准确地评价大草蛉种群质量。
本发明所提供的一种用精巢特异蛋白基因评价昆虫群体质量的方法,包括大草蛉雄虫精巢特异蛋白基因cDNA序列,以及通过检测此精巢特异蛋白基因的表达水平,全面、快捷、高效地评价大草蛉种群质量。
上述昆虫具体可以为大草蛉(Chrysopa pallens)。
上述精巢特异蛋白基因的核苷酸序列为序列表中的SEQ ID NO:1所示的序列,氨基酸序列为序列表中的SEQ ID NO:2所示的序列。
上述用精巢特异蛋白基因评价昆虫群体质量的方法,是用实时荧光PCR检测精巢特异蛋白基因的表达水平,预测大草蛉雄虫寿命情况,及与其交配后雌虫的繁殖能力。
下面通过具体实施例来进一步介绍。在实施例中,检测两种大草蛉雄虫精巢特异蛋白基因的表达水平,预测雄虫的寿命及与雌虫交配后雌虫的繁殖能力。
实施例1检测雄虫精巢特异蛋白基因表达
设两个处理组,羽化后将大草蛉雌虫与雄虫配对,用蚕豆蚜饲养,温度为26-27℃,相对湿度为60%。
处理组1为野外采集的大草蛉个体在室内饲养得到的第1代成虫;处理组2为野外采集的大草蛉个体在室内饲养得到的第20代成虫。
1.1提取整虫总RNA
采用北京兰易科技有限公司的LanEasy高纯总RNA快速提取试剂盒提取总RNA,型号LY-0003。提取整虫总RNA的方法包括以下步骤:
(1)羽化后第5天,将大草蛉单头雄成虫在液氮中磨碎,每个处理随机挑选4头。每50-100mg组织中加1ml的裂解液RL后匀浆,将匀浆样品剧烈震荡混匀,在15-30℃条件下孵育5分钟以使核蛋白体完全裂解。
(2)每1ml裂解液RL加0.2ml氯仿,盖紧样品管盖,剧烈震荡15秒并将其在室温下静置3分钟。
(3)于4℃条件下,12,000rpm离心10分钟,样品分成三层:下层有机相,中间层和上层无色的水相,RNA存在于水相中,取上层水相小心转移到新管中(不要碰到中间层),记录水相体积。
(4)加入水相体积一半的无水乙醇,混匀,将得到的溶液一起转入吸附柱RA中,12,000rpm离心1分钟,弃废液,将吸附柱重新套回收集管中。
(5)加入500μl去蛋白液RE,12,000rpm离心1分钟,弃废液。
(6)加入500μl漂洗液RW,12,000rpm离心1分钟,弃废液。
(7)重复步骤(6)一次。
(8)将吸附柱RA放回空收集管中,13,000rpm离心2分钟,尽量去除漂洗液。
(9)取出吸附柱RA,放入一个RNase free离心管中,在吸附柱中间部位加入50μlRNase free water,室温静置2分钟,12,000rpm离心1分钟。将所得样品在-80℃冰箱中保存。
1.2RNA质量检测
(1)分光光度计检测RNA浓度和纯度:吸取1μl RNA样品检测其浓度及OD260/OD280、OD260/OD230。
(2)琼脂糖凝胶电泳检测RNA完整性:取5μl样品与1μl 6x DNA loading buffer混匀,点入胶孔中,140V,15min,于凝胶成像仪下,根据条带分布和亮度判断RNA是否完整。
1.3去除第一链cDNA的合成及gDNA
使用北京全式金生物技术有限公司的TransScript One-Step gDNA Removal andcDNA Synthesis SuperMix试剂盒获取cDNA,型号AT311。包括以下步骤:
(1)在离心管中加入以下组分:
(2)轻轻混匀,置于PCR仪中,42℃15分钟。
(3)85℃加热5秒。
(4)将反应产物放于-20℃保存。
1.4实时荧光定量PCR检测
采用实时荧光定量PCR检测tbp基因,选择actin基因作为内参基因。
使用翌圣生物科技(上海)股份有限公司的Hieff Universal BlueqPCR SYBR Master Mix(型号11184ES08)配制反应体系。
(1)根据转录组数据中的序列,利用Primer Premier5.0软件设计qPCR引物,以cDNA为模板(即步骤1.3获得的反应产物),按照下列反应体系,在冰上配制。每头个体设置3个技术重复。
(2)扩增程序:
表1荧光定量引物序列
表1中所有引物均在生工生物工程(上海)股份有限公司合成。
表1中,引物qCpTBP-F为扩增tbp基因部分片段的正向引物,引物qCpTBP-R为扩增tbp基因部分片段的反向引物;引物actin-F为扩增actin基因部分片段的正向引物,引物actin-R为扩增actin基因部分片段的反向引物。
(3)实时荧光定量PCR检测结果:
如图1所示,扩增雄虫精巢特异蛋白基因tbp与内参基因actin的引物的熔解曲线都呈现单峰,说明两对引物的特异性好,扩增效率高。表2为内参基因actin与tbp基因的ct值。如图2所示,第20代雄成虫tbp的表达水平显著低于第1代雄成虫tbp的表达水平。两个处理组tbp的相对表达水平如图2所示。基因的相对表达水平采用2^-△△CT方法计算,计算公式为:△△CT=(Ct目的基因-Ct内参基因)实验组-(Ct目的基因-Ct内参基因)对照组。目的基因相对表达量=2^-△△CT,表示的是实验组目的基因表达量相对于对照组目的基因表达量的倍数。
表2各处理基因表达定量检测ct值
从表2中可以看出,第1代的ct值之差为15.73,说明群体的质量正常;第20代的ct值之差大于15.73时,说明群体的质量下降。
实施例2雄虫寿命与雌虫繁殖能力检测
对上述第1代大草蛉、第20代大草蛉分别检测大草蛉的产卵总量、寿命、卵重和孵化率等指标。
检测方法及结果如下:
取野外采集的大草蛉个体在室内饲养后得到的第1代成虫36对,野外采集的个体在室内饲养后得到的第20代成虫33对。羽化后将雌雄虫配对饲养,每日观察雄虫存活,雄虫全部死亡后,统计雄虫寿命,第20代雄虫寿命显著缩短(图4)。每日记录雌虫产卵量,统计产卵总量,第20代雌雄虫交配后产卵总量显著减少(图3)。羽化后第2周每天随机挑选卵100粒以上,用分析天平称重,统计卵重,第20代雌雄虫交配后产的卵显著减轻(图5)。称重后将卵保留,置于光照培养箱,观察孵化,及时将孵出的幼虫转移走,每日观察与转移3次,计算孵化率,第20代雌雄虫交配后产的卵孵化率显著下降(图6)。由此可见,当大草蛉雄成虫的两个基因ct值之差(tbp基因ct值-actin基因ct值)小于15.73时,雄虫寿命将短于33.03天,同一群体中雌虫产卵总量将低于980粒,卵重将低于110.97微克/粒,卵孵化率将低于89.8%。当大草蛉雄成虫的两个基因ct值之差(tbp基因ct值-actin基因ct值)为16.93时,雄虫寿命将缩短至约28.21天,同一群体中雌虫产卵总量将下降到约527粒,卵重将下降到约99.19微克/粒,卵孵化率将下降到约43.8%。
以上所述仅为本发明的较佳实施例,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
序列表
<110> 中国农业科学院植物保护研究所
<120> 一种用精巢特异蛋白基因评价昆虫种群质量的方法
<160> 6
<170> SIPOSequenceListing 1.0
<210> 1
<211> 9201
<212> DNA
<213> 大草蛉(Chrysopa pallens)
<400> 1
atggcatctt ttgtttttaa aactgaagct tacccaaaaa caacgggttt ttataaaaaa 60
actttttatc caccttcacg agttgatttg tatgatgaag ctcaatattg ttatacaaca 120
ggtgatgaga atttagtttc ttggtttgag caagtttttg ataggaattt taaaaaaaat 180
tctaatatta cttataattt attagaagta gaatatgata ataaacaata tcatattgtt 240
actgaaatta atggtttata taaaaggacc gtttattata ggattgatga agtatgggag 300
tatagtcctg aattaggaaa attgggattt gtatatttta aaagagtaaa tgttgatcca 360
ttgcctatat atcagcattt gagtattgac caagatgtta taggagagtt cactggtgat 420
gaattatatt gtgatagttg tgttgcacct ttaaaatcag agtgcaattg tatttataaa 480
aatattgtta atcgtgtagt caagcataag atcgataaaa tgtcatttca tacatattcg 540
caattagtat cacagtttgt tgatcaatcg ccattaccat ctagatctat tatgttacta 600
tataaaatta aagttttgat agataagttg aaaagtattc gatgtaatat tattcaatta 660
aaacgatttg attttagagc tcataatagt atagaaaaag cagttgaggc tctagaatta 720
gagtatatcc aacctgaaat gcctggagat acgccattag atgatttagt ggatcaacaa 780
catcctgata aagctagtac tactgtttta acgactcatt ctgaagttac gcaagttaaa 840
gaagaaccct ctatcatgaa agattatttt tctaaagctt cttcagcaga tggtttgcat 900
actttttctt atttaacaga taggtggatt ttattgcaaa agaaaacatg gaatgttaag 960
aaattaacaa ctgacaccat ggtttctttg agattatttg gtgatgtatt atcaacattg 1020
aaggaatctc ctgtaactag tatgtttaat tattttgcat atatgaagac agatttagtt 1080
tttagagttc atataaatac atctcaattc catgtgggtc aattgatagc tgctttttat 1140
tattcagcag cgttagataa ttatgaaaat atgcgatata ctgttgcagg attattgcaa 1200
atgcctcatg ttaaaattga tgctagtaaa gctaatgagg tagagcttgt tataccatat 1260
aaatattata aaagtatgat acgtttaaaa ccaacagcat attctgatga ttattcatat 1320
ggacgtttta tggttatgcc tattgttcct ataacaacaa gaggagggtg taaaaatgtt 1380
gatgtatcag tttttgttaa atttcagaat acggtatttt caggtctagt gccaaaagaa 1440
tttaaagtaa catctcgttt attaaaaaca gattcagatg atgaatatga ttatattcag 1500
cctgaaatga tgagtataaa gaagatagtg aacgctacga gtgatacttt ggatatgttg 1560
ataccagatc ccaatcgaga tgatcctcct agtacggata ttatacctac gcgaattata 1620
ccttctatgg cttcaaattg gtcatcagga aggaatgata ttgattttac agagagtatg 1680
cgtttaatac ctcagggcca gactcctcat cctattggaa gttctgataa tgttgaaact 1740
aatattttag cgatagcgag aaaacctggc ttattgagac aattagtttg ggatttaaat 1800
gaaaaaacac ctattacgcc tagtttgatt atacctgtag atcctatata tgatcctaca 1860
caagatactg attataagct atcagatgtt gaaaaaactt tgataacaat ttcagctaca 1920
actatgggtg ttggaaaaac ggcgtggttt gcccccccta taacacatat taccaatttt 1980
atgcaatatt ggagaggtag tatagtttat acatttgagg ttattagttc accttatcaa 2040
acaggttctg taatttgtgc atttattcct agtgttactg taattaaagc taaggagtat 2100
acgatagcag acttaagatc ttgttataat gctgtttttg atattcgtga aactcgtact 2160
tttaaattta gagtccctta tatagcagat aaaccatggt ggccaagatt agcgaatatg 2220
catctcgaaa atagtcctta ttatgtgatg gaacctacgg gtgtattatg ctttgctgag 2280
ttaaatcgta tgtgtgtttc ttctgcagct cctttacaac tatggattaa tgtttatgtg 2340
gaagctggag atgattttga attagctata cctacaacac ctttgtatag taatgtttat 2400
gataattcta tatatatttc atctgtagtt cgaattaaag aaggatatta tccagatttg 2460
tggtttgatg agtggcagta ttgtaaaggt aaactttgtt ttagatatgg ggaaggttct 2520
gatcatatta cacaatttgt gggtgatgtt aatcctacca cagtatataa agtaaataca 2580
ccaagtgcaa agacgagaat gtatatgaat acgttagctg gtggtataca gcaagttgtt 2640
tatgccgtca gtttaattgt taatggagat aaagatacat ataaatatat gaccccattt 2700
tataaattga gtgatgcgaa agcttttgca gcaaagaata agggttgggc tgattctgat 2760
cagacgttga tggtaggtaa cggtggtgcg tatcaagcta atagaactaa tgttaatgat 2820
tatggtgata tgtatttaga accaatttct accgttgcta gaccagagat ggatcaagaa 2880
caacctattt tagatccttc agttcatagt ttagcatcta caatgtctgg attaatgact 2940
tttggagaaa agtttgtgga tttgaaagat ataaatagaa ggtacaatca tgaaactact 3000
atagtgttac ctgttaaatg gggagattct acatcaactt ttgttcaaaa ttctgttagg 3060
tgtaagattc ctgttacaac agctggaata caattgaaag ctaatgatct ttatgacatg 3120
atagttagac aatctataat taattattct acttcagcat tcagatttag tagaggttca 3180
ctgagatatc gtttggtttt tgaatctcct ggtgattata atgttaaagt acaacatatt 3240
ccagaaattt tgttaacacc tcgtaatgtg cagcttttac ccagtggttc aaagaaatat 3300
cgagatttta ttaaacctgg ttattctatt attgaacaga atatcagaat taatccatgt 3360
attacaatag aagttccttt ttataaccct ggagttttta ttttaaatgg tgagcctaat 3420
atggaatatc aaacagaatt tccacatttt acatctggtt atttggctat atcgatagat 3480
attactccta agataagtga gtatattaat acaaatgtag gtagtttagt tatttctgtg 3540
tataaggcat atggtgatga ttttagtcca tctgtatatg taggttttcc tcctataata 3600
aagaaggttg aatatctaaa gggagatgat aaaatcactg cagaaccaga aatgatgtct 3660
tctattaaaa ctgggttgga ttatgttaat ccagttaata ttggaacaaa gttctgtaca 3720
gctgtaggaa gtaatgtggt taaagaggct aaagaagcta tatatgaagg ttgcacggat 3780
attatggata atataaaaaa ttcaaaacct ttgcagacaa ttatggatat gtttccagca 3840
tgtaatcgta cattattgat ttctgtattg actactatta ttatttgtgt tataaatcct 3900
aatattaaaa caattgctgt ttctattatt tcatattttg cacaagttgg catgattgca 3960
ttagatagtg taacaagatt agctaaagta tttgctgatt atttgtataa tttagttaaa 4020
gagaaaccaa aatttgaacc ttctcaatta cgtagtgttg tgaaatatgc tgtggatatg 4080
aaaattttaa cgggtaattc tagctgttta ataccttatg tattagaaga tgttcttacg 4140
aatcaacagt cacaagtaag aatacctata gtgcctaggg tagtgagaga aggagattat 4200
gataaagaag ttatacaatc tatgatagtt aagtgtaaga aaattcataa ggaattgatt 4260
atatatttgt ctcaacaagt aacagaagag tatgcaaaac agatgattga tatagcgatt 4320
gaaaagtatg ataattattc gttgcacgat ataaatagtt tacaacctac tgtttttatt 4380
tataagaatg gttacgttaa tgactctgat gtagactcat tatattatga tagcattatt 4440
aatcaaccga gtacatcaca tgaagtacaa ccagagggtt ttgcagattt tatggatcat 4500
actcctgctg tagtatcaac atcgattata gcaattttag gaatattaaa agttggaaag 4560
tctacattaa agtggaattg tataccagat tttggaaaaa ccttattaca tgatattaaa 4620
gatttttctt taacagctaa tcatttgttt atatttttta ggaatacggc atctatgttt 4680
aaagatatgt ttttgtggat aagtcgtaag tgttgtcctg aaaatagatt tttatcatcc 4740
ttagtacatg ataagcaaca tatctgtcaa tggatagaag aagctaattg ggtgttagat 4800
gaggcaaatg ataagttgat tcgatcaaat cctagatata cattacgagt atattatgca 4860
gcgttttttg cagaacaatt gcgcaaacag tacattactg ctgattcatc aactttgaca 4920
cgtttacggt gtttagaaca gttgtttaaa gctgttataa ataaacgtaa tgagttacag 4980
acagatcggt tatgtcccga agtccgtgaa gaaccgtttg ttttatcttt ggatggcgat 5040
acaaatgtag gaaaatcgca tttgggaagt actatttcat atcatttagc aaagaagtat 5100
aagtggtgca ctggtggcga aattatttat gttaaagctc ctaataataa atattataat 5160
ggtttaaaaa atcagcctgt attgttattt gatgattttg ctcagattaa tgaagaaaat 5220
ccatatttat tagatcaaat tacagatttg tttaatttaa agtcatctgc tatttataat 5280
cctcctatgg ctgcagtaga agaaaagaat ttgaggtata atccaaagct tgttgttttg 5340
tgtactaata ccccgtatcc tgtaccacaa ggtatagcta gtgtttctgc ttttcataga 5400
cgaagggata tgatgattag tatcagatgg aagaaggagt ttaaggataa aacagtttta 5460
acattaccat ctattataaa gaatacatat caacatttac aatttgcgat tcgagctagt 5520
tcaactaaga atgatgttat tccagaagat gcttggttag attctttgga agaactttat 5580
gaaaaaatag aagagaggta tgatgctttt tatgagaatg aatctaataa tttccaaatg 5640
cgattaaata gattacgaag tgttcaagaa gagaatttgg atatattaag tttgaatgct 5700
attaaggaag aataccatgc tgttatagct ttagcggcat cacaaggtac ttatgattat 5760
gcaccattaa aacaacaggt tatggaaaca tatagtggat acaatataga aaagaagcgt 5820
aagtattgta ctcttttaaa taagaatata gaaatggaat catctaatat atttgaagat 5880
atcacaagtg ctttagaagc gatggatttg aaagttcaac ctgaagctga ttttgcgatt 5940
gaagaaaatg tagattgtat gcatttattg tgttttcctg aaacattaaa aggctttgat 6000
attacaaaat tgaaagatag tatatatata agtaggaagg aagttgagag ttgtgtaagt 6060
ccagctttat tgaatgaaga agtttcagag atatatagag aaatgtttaa aggaaataca 6120
gagtggaatt taagttcgtt taatgaaggc ttatttatat tacctcaatc aaagtctttt 6180
ataccagttc ctgttgctaa gtgttgtaaa aaaggaaaag gaacaacaga ttgtattatg 6240
catgatgaat tagtatatca aagttttaga aaggctatta aatactggtt tgataattta 6300
gtagaagatg agagacaatt tctgttaaga ttttcaaaag gagaaaaagc agaggataat 6360
catttacctt ttatattatt aaaagatttg ttgtttgaaa aaactcctgt aaaaatttct 6420
aaagcttttg aggaatgtgt tcaaaatgct gaaaaagatg taacttggtt atcgaaagga 6480
gttcgttata tttggacatt gattaaaggt ttgacttggg ttttatgtaa aatggcatcg 6540
tacgcagtat tctttggtgg aatgtctgct ttagtaactt tttccaaccc attatctgag 6600
tcaaatattc gaaacggtat aaacggtgct atagtgaaaa caacaaaaga tttaacaggt 6660
tcaaatattg cagctactgc tatgggatta gttgttcaca aaggagattt aggttcgtca 6720
ttaaaaagtg ttataggaac agaagtactt tggggtggga agaaaaatcc agagatgtct 6780
tatacacaat ataatacgaa agctgtccct actattcagg gcgctattaa gataataaga 6840
ccagagatgg cagatgaaat ctattcaaat ttgaggcgca tcattcggag aaacacagta 6900
tttatcagag tgcaaaaagt agattcatat attgatatga gaggaatagg gttgtgtggt 6960
actaatattt tggtagtaga tcatatggtt gattatataa gaaagagttt tgatgatgat 7020
agtgttgaaa aaattttagt ttttattaac ggtatgattt atgaaattca gcaaggtgat 7080
attgatgttt tattattgga agattcagta tatcgtatta taaattgtaa gtttcatatg 7140
ccaaaattta aatcattagt aaaatatatg caaaatcaaa aagctagtgg cgcatgtgct 7200
ccagatgggt atttagttga acctacttta attatagata aagctaaacc atcaacatat 7260
acagtagata taacgataca tcgacaatct actttagaag ttgcgcataa tgtagcaata 7320
acaggtgata aatcaaaagg tatacaacca tcttgtgcta gagattgtta tacatatcaa 7380
acatctggtt taggtaaatg tatgtctgtt ttgttagcta attataatac tccctcaccc 7440
ataataggtt ttcatgttgc tggtttgaaa tctggaaata aaggttttgc agagttaata 7500
gtttctgaat cgtttcaatc tttgataaat aaagacttag atgttataga acctgagatg 7560
gctccggttg aatttgcaca tcaacaatta gatacaaatg tgatacagat aggagtttta 7620
gcaaaagagt atcatcaacg tattactaaa gaatcaaaac aaaggcatag tgtgatttat 7680
aacaaattcc atgagtcaac atatgatttt cctgttttaa caagaactga cgaaagaatt 7740
aagaatgatc cattttcacc attattagaa ggttgtaaat tgcatggtaa agtgcctcat 7800
gaatttgata aagatttatt agatatttgt gctaaagatt tatctcatac gttaaaaaca 7860
aagtgtcctc ctattcgtaa atatgctcaa ctattaacag atcaagtagc agtgtgtgga 7920
gatccaatgg catcagatct ttatcagcct atagatttat ccacaagtga aggcttcccg 7980
tattccaaat ttagaccaca aggtttttct tcaaaacgat ggttatttga tataaattat 8040
aatagtaatt atccccagtt aatctctata catcctatgg ttcaagaaat tagagatata 8100
aagaaaatac aacgtttaaa taatcaaatt ccctttacat tatttactga tagtttaaaa 8160
gatttaaaga tgcctgctga aaagtgtatt atacctggaa agactagggt gttttcactc 8220
tgtcctgtag attttttatt ggatgtaaga gtttattttg gtgattttgt ggcttcttat 8280
acaaaggcta ggttatcagc tgagcatgct gttggaatta atgtaaattc atatgagtgg 8340
acagatcttg ctaattactt attatcaaat agtgaacata tagttacagg tgattataaa 8400
aattttggcc ctacattaat ggctgcttgt gttagtaaag cttttgaaat aattagagaa 8460
tggtatcatt ttaattcaaa ggattttaaa gttgatccaa atgatgattt aattagatat 8520
attttaggat atgagatgac gtattcttat caccttatgg aagatcttgt atatcaagtc 8580
tgttgtggcg ctccttcagg atcgccacta acagtagttt taaataattt ggttaatggg 8640
ttatatatcc gttatgcttg gttgtgttta atgaaaaata caggtatata ttcatcttta 8700
aaagattttc atgataatgt aagagttatt ttctatggtg atgatataat aatgagtgtt 8760
aaggaatgtg ttttggaata ttttaatgct aaaaagattt cagatttgtt tgcacaatat 8820
aatattattt ttacagattc ggcaaagtct aattgtatta aaccttcatc ttcgttatat 8880
gatgaagaaa ctacattttt aaaatgtcat tttgttccac atccatacag atctggtact 8940
atattaccgc gtatagataa aagagcaatt ttagaagttc ctaattggat ttttaaaaca 9000
aaagatgaat atgcagctac tgctcaagca attcaaagca tgtttgttgg tttatatggt 9060
catggtgaag aattttatga gcataataaa gaaaaaatta taagaatttt aaaagagaat 9120
gaaatgttat atcatccatc attcagaaat ttaaatatac catcttggag agatgtagat 9180
ttaaaaaatt taggtatgta a 9201
<210> 2
<211> 3066
<212> PRT
<213> 大草蛉(Chrysopa pallens)
<400> 2
Met Ala Ser Phe Val Phe Lys Thr Glu Ala Tyr Pro Lys Thr Thr Gly
1 5 10 15
Phe Tyr Lys Lys Thr Phe Tyr Pro Pro Ser Arg Val Asp Leu Tyr Asp
20 25 30
Glu Ala Gln Tyr Cys Tyr Thr Thr Gly Asp Glu Asn Leu Val Ser Trp
35 40 45
Phe Glu Gln Val Phe Asp Arg Asn Phe Lys Lys Asn Ser Asn Ile Thr
50 55 60
Tyr Asn Leu Leu Glu Val Glu Tyr Asp Asn Lys Gln Tyr His Ile Val
65 70 75 80
Thr Glu Ile Asn Gly Leu Tyr Lys Arg Thr Val Tyr Tyr Arg Ile Asp
85 90 95
Glu Val Trp Glu Tyr Ser Pro Glu Leu Gly Lys Leu Gly Phe Val Tyr
100 105 110
Phe Lys Arg Val Asn Val Asp Pro Leu Pro Ile Tyr Gln His Leu Ser
115 120 125
Ile Asp Gln Asp Val Ile Gly Glu Phe Thr Gly Asp Glu Leu Tyr Cys
130 135 140
Asp Ser Cys Val Ala Pro Leu Lys Ser Glu Cys Asn Cys Ile Tyr Lys
145 150 155 160
Asn Ile Val Asn Arg Val Val Lys His Lys Ile Asp Lys Met Ser Phe
165 170 175
His Thr Tyr Ser Gln Leu Val Ser Gln Phe Val Asp Gln Ser Pro Leu
180 185 190
Pro Ser Arg Ser Ile Met Leu Leu Tyr Lys Ile Lys Val Leu Ile Asp
195 200 205
Lys Leu Lys Ser Ile Arg Cys Asn Ile Ile Gln Leu Lys Arg Phe Asp
210 215 220
Phe Arg Ala His Asn Ser Ile Glu Lys Ala Val Glu Ala Leu Glu Leu
225 230 235 240
Glu Tyr Ile Gln Pro Glu Met Pro Gly Asp Thr Pro Leu Asp Asp Leu
245 250 255
Val Asp Gln Gln His Pro Asp Lys Ala Ser Thr Thr Val Leu Thr Thr
260 265 270
His Ser Glu Val Thr Gln Val Lys Glu Glu Pro Ser Ile Met Lys Asp
275 280 285
Tyr Phe Ser Lys Ala Ser Ser Ala Asp Gly Leu His Thr Phe Ser Tyr
290 295 300
Leu Thr Asp Arg Trp Ile Leu Leu Gln Lys Lys Thr Trp Asn Val Lys
305 310 315 320
Lys Leu Thr Thr Asp Thr Met Val Ser Leu Arg Leu Phe Gly Asp Val
325 330 335
Leu Ser Thr Leu Lys Glu Ser Pro Val Thr Ser Met Phe Asn Tyr Phe
340 345 350
Ala Tyr Met Lys Thr Asp Leu Val Phe Arg Val His Ile Asn Thr Ser
355 360 365
Gln Phe His Val Gly Gln Leu Ile Ala Ala Phe Tyr Tyr Ser Ala Ala
370 375 380
Leu Asp Asn Tyr Glu Asn Met Arg Tyr Thr Val Ala Gly Leu Leu Gln
385 390 395 400
Met Pro His Val Lys Ile Asp Ala Ser Lys Ala Asn Glu Val Glu Leu
405 410 415
Val Ile Pro Tyr Lys Tyr Tyr Lys Ser Met Ile Arg Leu Lys Pro Thr
420 425 430
Ala Tyr Ser Asp Asp Tyr Ser Tyr Gly Arg Phe Met Val Met Pro Ile
435 440 445
Val Pro Ile Thr Thr Arg Gly Gly Cys Lys Asn Val Asp Val Ser Val
450 455 460
Phe Val Lys Phe Gln Asn Thr Val Phe Ser Gly Leu Val Pro Lys Glu
465 470 475 480
Phe Lys Val Thr Ser Arg Leu Leu Lys Thr Asp Ser Asp Asp Glu Tyr
485 490 495
Asp Tyr Ile Gln Pro Glu Met Met Ser Ile Lys Lys Ile Val Asn Ala
500 505 510
Thr Ser Asp Thr Leu Asp Met Leu Ile Pro Asp Pro Asn Arg Asp Asp
515 520 525
Pro Pro Ser Thr Asp Ile Ile Pro Thr Arg Ile Ile Pro Ser Met Ala
530 535 540
Ser Asn Trp Ser Ser Gly Arg Asn Asp Ile Asp Phe Thr Glu Ser Met
545 550 555 560
Arg Leu Ile Pro Gln Gly Gln Thr Pro His Pro Ile Gly Ser Ser Asp
565 570 575
Asn Val Glu Thr Asn Ile Leu Ala Ile Ala Arg Lys Pro Gly Leu Leu
580 585 590
Arg Gln Leu Val Trp Asp Leu Asn Glu Lys Thr Pro Ile Thr Pro Ser
595 600 605
Leu Ile Ile Pro Val Asp Pro Ile Tyr Asp Pro Thr Gln Asp Thr Asp
610 615 620
Tyr Lys Leu Ser Asp Val Glu Lys Thr Leu Ile Thr Ile Ser Ala Thr
625 630 635 640
Thr Met Gly Val Gly Lys Thr Ala Trp Phe Ala Pro Pro Ile Thr His
645 650 655
Ile Thr Asn Phe Met Gln Tyr Trp Arg Gly Ser Ile Val Tyr Thr Phe
660 665 670
Glu Val Ile Ser Ser Pro Tyr Gln Thr Gly Ser Val Ile Cys Ala Phe
675 680 685
Ile Pro Ser Val Thr Val Ile Lys Ala Lys Glu Tyr Thr Ile Ala Asp
690 695 700
Leu Arg Ser Cys Tyr Asn Ala Val Phe Asp Ile Arg Glu Thr Arg Thr
705 710 715 720
Phe Lys Phe Arg Val Pro Tyr Ile Ala Asp Lys Pro Trp Trp Pro Arg
725 730 735
Leu Ala Asn Met His Leu Glu Asn Ser Pro Tyr Tyr Val Met Glu Pro
740 745 750
Thr Gly Val Leu Cys Phe Ala Glu Leu Asn Arg Met Cys Val Ser Ser
755 760 765
Ala Ala Pro Leu Gln Leu Trp Ile Asn Val Tyr Val Glu Ala Gly Asp
770 775 780
Asp Phe Glu Leu Ala Ile Pro Thr Thr Pro Leu Tyr Ser Asn Val Tyr
785 790 795 800
Asp Asn Ser Ile Tyr Ile Ser Ser Val Val Arg Ile Lys Glu Gly Tyr
805 810 815
Tyr Pro Asp Leu Trp Phe Asp Glu Trp Gln Tyr Cys Lys Gly Lys Leu
820 825 830
Cys Phe Arg Tyr Gly Glu Gly Ser Asp His Ile Thr Gln Phe Val Gly
835 840 845
Asp Val Asn Pro Thr Thr Val Tyr Lys Val Asn Thr Pro Ser Ala Lys
850 855 860
Thr Arg Met Tyr Met Asn Thr Leu Ala Gly Gly Ile Gln Gln Val Val
865 870 875 880
Tyr Ala Val Ser Leu Ile Val Asn Gly Asp Lys Asp Thr Tyr Lys Tyr
885 890 895
Met Thr Pro Phe Tyr Lys Leu Ser Asp Ala Lys Ala Phe Ala Ala Lys
900 905 910
Asn Lys Gly Trp Ala Asp Ser Asp Gln Thr Leu Met Val Gly Asn Gly
915 920 925
Gly Ala Tyr Gln Ala Asn Arg Thr Asn Val Asn Asp Tyr Gly Asp Met
930 935 940
Tyr Leu Glu Pro Ile Ser Thr Val Ala Arg Pro Glu Met Asp Gln Glu
945 950 955 960
Gln Pro Ile Leu Asp Pro Ser Val His Ser Leu Ala Ser Thr Met Ser
965 970 975
Gly Leu Met Thr Phe Gly Glu Lys Phe Val Asp Leu Lys Asp Ile Asn
980 985 990
Arg Arg Tyr Asn His Glu Thr Thr Ile Val Leu Pro Val Lys Trp Gly
995 1000 1005
Asp Ser Thr Ser Thr Phe Val Gln Asn Ser Val Arg Cys Lys Ile Pro
1010 1015 1020
Val Thr Thr Ala Gly Ile Gln Leu Lys Ala Asn Asp Leu Tyr Asp Met
1025 1030 1035 1040
Ile Val Arg Gln Ser Ile Ile Asn Tyr Ser Thr Ser Ala Phe Arg Phe
1045 1050 1055
Ser Arg Gly Ser Leu Arg Tyr Arg Leu Val Phe Glu Ser Pro Gly Asp
1060 1065 1070
Tyr Asn Val Lys Val Gln His Ile Pro Glu Ile Leu Leu Thr Pro Arg
1075 1080 1085
Asn Val Gln Leu Leu Pro Ser Gly Ser Lys Lys Tyr Arg Asp Phe Ile
1090 1095 1100
Lys Pro Gly Tyr Ser Ile Ile Glu Gln Asn Ile Arg Ile Asn Pro Cys
1105 1110 1115 1120
Ile Thr Ile Glu Val Pro Phe Tyr Asn Pro Gly Val Phe Ile Leu Asn
1125 1130 1135
Gly Glu Pro Asn Met Glu Tyr Gln Thr Glu Phe Pro His Phe Thr Ser
1140 1145 1150
Gly Tyr Leu Ala Ile Ser Ile Asp Ile Thr Pro Lys Ile Ser Glu Tyr
1155 1160 1165
Ile Asn Thr Asn Val Gly Ser Leu Val Ile Ser Val Tyr Lys Ala Tyr
1170 1175 1180
Gly Asp Asp Phe Ser Pro Ser Val Tyr Val Gly Phe Pro Pro Ile Ile
1185 1190 1195 1200
Lys Lys Val Glu Tyr Leu Lys Gly Asp Asp Lys Ile Thr Ala Glu Pro
1205 1210 1215
Glu Met Met Ser Ser Ile Lys Thr Gly Leu Asp Tyr Val Asn Pro Val
1220 1225 1230
Asn Ile Gly Thr Lys Phe Cys Thr Ala Val Gly Ser Asn Val Val Lys
1235 1240 1245
Glu Ala Lys Glu Ala Ile Tyr Glu Gly Cys Thr Asp Ile Met Asp Asn
1250 1255 1260
Ile Lys Asn Ser Lys Pro Leu Gln Thr Ile Met Asp Met Phe Pro Ala
1265 1270 1275 1280
Cys Asn Arg Thr Leu Leu Ile Ser Val Leu Thr Thr Ile Ile Ile Cys
1285 1290 1295
Val Ile Asn Pro Asn Ile Lys Thr Ile Ala Val Ser Ile Ile Ser Tyr
1300 1305 1310
Phe Ala Gln Val Gly Met Ile Ala Leu Asp Ser Val Thr Arg Leu Ala
1315 1320 1325
Lys Val Phe Ala Asp Tyr Leu Tyr Asn Leu Val Lys Glu Lys Pro Lys
1330 1335 1340
Phe Glu Pro Ser Gln Leu Arg Ser Val Val Lys Tyr Ala Val Asp Met
1345 1350 1355 1360
Lys Ile Leu Thr Gly Asn Ser Ser Cys Leu Ile Pro Tyr Val Leu Glu
1365 1370 1375
Asp Val Leu Thr Asn Gln Gln Ser Gln Val Arg Ile Pro Ile Val Pro
1380 1385 1390
Arg Val Val Arg Glu Gly Asp Tyr Asp Lys Glu Val Ile Gln Ser Met
1395 1400 1405
Ile Val Lys Cys Lys Lys Ile His Lys Glu Leu Ile Ile Tyr Leu Ser
1410 1415 1420
Gln Gln Val Thr Glu Glu Tyr Ala Lys Gln Met Ile Asp Ile Ala Ile
1425 1430 1435 1440
Glu Lys Tyr Asp Asn Tyr Ser Leu His Asp Ile Asn Ser Leu Gln Pro
1445 1450 1455
Thr Val Phe Ile Tyr Lys Asn Gly Tyr Val Asn Asp Ser Asp Val Asp
1460 1465 1470
Ser Leu Tyr Tyr Asp Ser Ile Ile Asn Gln Pro Ser Thr Ser His Glu
1475 1480 1485
Val Gln Pro Glu Gly Phe Ala Asp Phe Met Asp His Thr Pro Ala Val
1490 1495 1500
Val Ser Thr Ser Ile Ile Ala Ile Leu Gly Ile Leu Lys Val Gly Lys
1505 1510 1515 1520
Ser Thr Leu Lys Trp Asn Cys Ile Pro Asp Phe Gly Lys Thr Leu Leu
1525 1530 1535
His Asp Ile Lys Asp Phe Ser Leu Thr Ala Asn His Leu Phe Ile Phe
1540 1545 1550
Phe Arg Asn Thr Ala Ser Met Phe Lys Asp Met Phe Leu Trp Ile Ser
1555 1560 1565
Arg Lys Cys Cys Pro Glu Asn Arg Phe Leu Ser Ser Leu Val His Asp
1570 1575 1580
Lys Gln His Ile Cys Gln Trp Ile Glu Glu Ala Asn Trp Val Leu Asp
1585 1590 1595 1600
Glu Ala Asn Asp Lys Leu Ile Arg Ser Asn Pro Arg Tyr Thr Leu Arg
1605 1610 1615
Val Tyr Tyr Ala Ala Phe Phe Ala Glu Gln Leu Arg Lys Gln Tyr Ile
1620 1625 1630
Thr Ala Asp Ser Ser Thr Leu Thr Arg Leu Arg Cys Leu Glu Gln Leu
1635 1640 1645
Phe Lys Ala Val Ile Asn Lys Arg Asn Glu Leu Gln Thr Asp Arg Leu
1650 1655 1660
Cys Pro Glu Val Arg Glu Glu Pro Phe Val Leu Ser Leu Asp Gly Asp
1665 1670 1675 1680
Thr Asn Val Gly Lys Ser His Leu Gly Ser Thr Ile Ser Tyr His Leu
1685 1690 1695
Ala Lys Lys Tyr Lys Trp Cys Thr Gly Gly Glu Ile Ile Tyr Val Lys
1700 1705 1710
Ala Pro Asn Asn Lys Tyr Tyr Asn Gly Leu Lys Asn Gln Pro Val Leu
1715 1720 1725
Leu Phe Asp Asp Phe Ala Gln Ile Asn Glu Glu Asn Pro Tyr Leu Leu
1730 1735 1740
Asp Gln Ile Thr Asp Leu Phe Asn Leu Lys Ser Ser Ala Ile Tyr Asn
1745 1750 1755 1760
Pro Pro Met Ala Ala Val Glu Glu Lys Asn Leu Arg Tyr Asn Pro Lys
1765 1770 1775
Leu Val Val Leu Cys Thr Asn Thr Pro Tyr Pro Val Pro Gln Gly Ile
1780 1785 1790
Ala Ser Val Ser Ala Phe His Arg Arg Arg Asp Met Met Ile Ser Ile
1795 1800 1805
Arg Trp Lys Lys Glu Phe Lys Asp Lys Thr Val Leu Thr Leu Pro Ser
1810 1815 1820
Ile Ile Lys Asn Thr Tyr Gln His Leu Gln Phe Ala Ile Arg Ala Ser
1825 1830 1835 1840
Ser Thr Lys Asn Asp Val Ile Pro Glu Asp Ala Trp Leu Asp Ser Leu
1845 1850 1855
Glu Glu Leu Tyr Glu Lys Ile Glu Glu Arg Tyr Asp Ala Phe Tyr Glu
1860 1865 1870
Asn Glu Ser Asn Asn Phe Gln Met Arg Leu Asn Arg Leu Arg Ser Val
1875 1880 1885
Gln Glu Glu Asn Leu Asp Ile Leu Ser Leu Asn Ala Ile Lys Glu Glu
1890 1895 1900
Tyr His Ala Val Ile Ala Leu Ala Ala Ser Gln Gly Thr Tyr Asp Tyr
1905 1910 1915 1920
Ala Pro Leu Lys Gln Gln Val Met Glu Thr Tyr Ser Gly Tyr Asn Ile
1925 1930 1935
Glu Lys Lys Arg Lys Tyr Cys Thr Leu Leu Asn Lys Asn Ile Glu Met
1940 1945 1950
Glu Ser Ser Asn Ile Phe Glu Asp Ile Thr Ser Ala Leu Glu Ala Met
1955 1960 1965
Asp Leu Lys Val Gln Pro Glu Ala Asp Phe Ala Ile Glu Glu Asn Val
1970 1975 1980
Asp Cys Met His Leu Leu Cys Phe Pro Glu Thr Leu Lys Gly Phe Asp
1985 1990 1995 2000
Ile Thr Lys Leu Lys Asp Ser Ile Tyr Ile Ser Arg Lys Glu Val Glu
2005 2010 2015
Ser Cys Val Ser Pro Ala Leu Leu Asn Glu Glu Val Ser Glu Ile Tyr
2020 2025 2030
Arg Glu Met Phe Lys Gly Asn Thr Glu Trp Asn Leu Ser Ser Phe Asn
2035 2040 2045
Glu Gly Leu Phe Ile Leu Pro Gln Ser Lys Ser Phe Ile Pro Val Pro
2050 2055 2060
Val Ala Lys Cys Cys Lys Lys Gly Lys Gly Thr Thr Asp Cys Ile Met
2065 2070 2075 2080
His Asp Glu Leu Val Tyr Gln Ser Phe Arg Lys Ala Ile Lys Tyr Trp
2085 2090 2095
Phe Asp Asn Leu Val Glu Asp Glu Arg Gln Phe Leu Leu Arg Phe Ser
2100 2105 2110
Lys Gly Glu Lys Ala Glu Asp Asn His Leu Pro Phe Ile Leu Leu Lys
2115 2120 2125
Asp Leu Leu Phe Glu Lys Thr Pro Val Lys Ile Ser Lys Ala Phe Glu
2130 2135 2140
Glu Cys Val Gln Asn Ala Glu Lys Asp Val Thr Trp Leu Ser Lys Gly
2145 2150 2155 2160
Val Arg Tyr Ile Trp Thr Leu Ile Lys Gly Leu Thr Trp Val Leu Cys
2165 2170 2175
Lys Met Ala Ser Tyr Ala Val Phe Phe Gly Gly Met Ser Ala Leu Val
2180 2185 2190
Thr Phe Ser Asn Pro Leu Ser Glu Ser Asn Ile Arg Asn Gly Ile Asn
2195 2200 2205
Gly Ala Ile Val Lys Thr Thr Lys Asp Leu Thr Gly Ser Asn Ile Ala
2210 2215 2220
Ala Thr Ala Met Gly Leu Val Val His Lys Gly Asp Leu Gly Ser Ser
2225 2230 2235 2240
Leu Lys Ser Val Ile Gly Thr Glu Val Leu Trp Gly Gly Lys Lys Asn
2245 2250 2255
Pro Glu Met Ser Tyr Thr Gln Tyr Asn Thr Lys Ala Val Pro Thr Ile
2260 2265 2270
Gln Gly Ala Ile Lys Ile Ile Arg Pro Glu Met Ala Asp Glu Ile Tyr
2275 2280 2285
Ser Asn Leu Arg Arg Ile Ile Arg Arg Asn Thr Val Phe Ile Arg Val
2290 2295 2300
Gln Lys Val Asp Ser Tyr Ile Asp Met Arg Gly Ile Gly Leu Cys Gly
2305 2310 2315 2320
Thr Asn Ile Leu Val Val Asp His Met Val Asp Tyr Ile Arg Lys Ser
2325 2330 2335
Phe Asp Asp Asp Ser Val Glu Lys Ile Leu Val Phe Ile Asn Gly Met
2340 2345 2350
Ile Tyr Glu Ile Gln Gln Gly Asp Ile Asp Val Leu Leu Leu Glu Asp
2355 2360 2365
Ser Val Tyr Arg Ile Ile Asn Cys Lys Phe His Met Pro Lys Phe Lys
2370 2375 2380
Ser Leu Val Lys Tyr Met Gln Asn Gln Lys Ala Ser Gly Ala Cys Ala
2385 2390 2395 2400
Pro Asp Gly Tyr Leu Val Glu Pro Thr Leu Ile Ile Asp Lys Ala Lys
2405 2410 2415
Pro Ser Thr Tyr Thr Val Asp Ile Thr Ile His Arg Gln Ser Thr Leu
2420 2425 2430
Glu Val Ala His Asn Val Ala Ile Thr Gly Asp Lys Ser Lys Gly Ile
2435 2440 2445
Gln Pro Ser Cys Ala Arg Asp Cys Tyr Thr Tyr Gln Thr Ser Gly Leu
2450 2455 2460
Gly Lys Cys Met Ser Val Leu Leu Ala Asn Tyr Asn Thr Pro Ser Pro
2465 2470 2475 2480
Ile Ile Gly Phe His Val Ala Gly Leu Lys Ser Gly Asn Lys Gly Phe
2485 2490 2495
Ala Glu Leu Ile Val Ser Glu Ser Phe Gln Ser Leu Ile Asn Lys Asp
2500 2505 2510
Leu Asp Val Ile Glu Pro Glu Met Ala Pro Val Glu Phe Ala His Gln
2515 2520 2525
Gln Leu Asp Thr Asn Val Ile Gln Ile Gly Val Leu Ala Lys Glu Tyr
2530 2535 2540
His Gln Arg Ile Thr Lys Glu Ser Lys Gln Arg His Ser Val Ile Tyr
2545 2550 2555 2560
Asn Lys Phe His Glu Ser Thr Tyr Asp Phe Pro Val Leu Thr Arg Thr
2565 2570 2575
Asp Glu Arg Ile Lys Asn Asp Pro Phe Ser Pro Leu Leu Glu Gly Cys
2580 2585 2590
Lys Leu His Gly Lys Val Pro His Glu Phe Asp Lys Asp Leu Leu Asp
2595 2600 2605
Ile Cys Ala Lys Asp Leu Ser His Thr Leu Lys Thr Lys Cys Pro Pro
2610 2615 2620
Ile Arg Lys Tyr Ala Gln Leu Leu Thr Asp Gln Val Ala Val Cys Gly
2625 2630 2635 2640
Asp Pro Met Ala Ser Asp Leu Tyr Gln Pro Ile Asp Leu Ser Thr Ser
2645 2650 2655
Glu Gly Phe Pro Tyr Ser Lys Phe Arg Pro Gln Gly Phe Ser Ser Lys
2660 2665 2670
Arg Trp Leu Phe Asp Ile Asn Tyr Asn Ser Asn Tyr Pro Gln Leu Ile
2675 2680 2685
Ser Ile His Pro Met Val Gln Glu Ile Arg Asp Ile Lys Lys Ile Gln
2690 2695 2700
Arg Leu Asn Asn Gln Ile Pro Phe Thr Leu Phe Thr Asp Ser Leu Lys
2705 2710 2715 2720
Asp Leu Lys Met Pro Ala Glu Lys Cys Ile Ile Pro Gly Lys Thr Arg
2725 2730 2735
Val Phe Ser Leu Cys Pro Val Asp Phe Leu Leu Asp Val Arg Val Tyr
2740 2745 2750
Phe Gly Asp Phe Val Ala Ser Tyr Thr Lys Ala Arg Leu Ser Ala Glu
2755 2760 2765
His Ala Val Gly Ile Asn Val Asn Ser Tyr Glu Trp Thr Asp Leu Ala
2770 2775 2780
Asn Tyr Leu Leu Ser Asn Ser Glu His Ile Val Thr Gly Asp Tyr Lys
2785 2790 2795 2800
Asn Phe Gly Pro Thr Leu Met Ala Ala Cys Val Ser Lys Ala Phe Glu
2805 2810 2815
Ile Ile Arg Glu Trp Tyr His Phe Asn Ser Lys Asp Phe Lys Val Asp
2820 2825 2830
Pro Asn Asp Asp Leu Ile Arg Tyr Ile Leu Gly Tyr Glu Met Thr Tyr
2835 2840 2845
Ser Tyr His Leu Met Glu Asp Leu Val Tyr Gln Val Cys Cys Gly Ala
2850 2855 2860
Pro Ser Gly Ser Pro Leu Thr Val Val Leu Asn Asn Leu Val Asn Gly
2865 2870 2875 2880
Leu Tyr Ile Arg Tyr Ala Trp Leu Cys Leu Met Lys Asn Thr Gly Ile
2885 2890 2895
Tyr Ser Ser Leu Lys Asp Phe His Asp Asn Val Arg Val Ile Phe Tyr
2900 2905 2910
Gly Asp Asp Ile Ile Met Ser Val Lys Glu Cys Val Leu Glu Tyr Phe
2915 2920 2925
Asn Ala Lys Lys Ile Ser Asp Leu Phe Ala Gln Tyr Asn Ile Ile Phe
2930 2935 2940
Thr Asp Ser Ala Lys Ser Asn Cys Ile Lys Pro Ser Ser Ser Leu Tyr
2945 2950 2955 2960
Asp Glu Glu Thr Thr Phe Leu Lys Cys His Phe Val Pro His Pro Tyr
2965 2970 2975
Arg Ser Gly Thr Ile Leu Pro Arg Ile Asp Lys Arg Ala Ile Leu Glu
2980 2985 2990
Val Pro Asn Trp Ile Phe Lys Thr Lys Asp Glu Tyr Ala Ala Thr Ala
2995 3000 3005
Gln Ala Ile Gln Ser Met Phe Val Gly Leu Tyr Gly His Gly Glu Glu
3010 3015 3020
Phe Tyr Glu His Asn Lys Glu Lys Ile Ile Arg Ile Leu Lys Glu Asn
3025 3030 3035 3040
Glu Met Leu Tyr His Pro Ser Phe Arg Asn Leu Asn Ile Pro Ser Trp
3045 3050 3055
Arg Asp Val Asp Leu Lys Asn Leu Gly Met
3060 3065
<210> 3
<211> 17
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 3
ctttggtgga atgtctg 17
<210> 4
<211> 17
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 4
aatcccatag cagtagc 17
<210> 5
<211> 22
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 5
aacttcccga cggtcaagtc at 22
<210> 6
<211> 22
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 6
tgttggcgta caagtcctta cg 22

Claims (7)

1.一种用精巢特异蛋白基因评价昆虫种群质量的方法,其特征在于,包括以下步骤:检测精巢特异蛋白基因的表达水平;精巢特异蛋白基因的核苷酸序列如SEQ ID NO:1所示;昆虫为大草蛉。
2.根据权利要求1所述方法,其特征在于,包括以下步骤:采用荧光定量PCR方法检测精巢特异蛋白基因的表达水平;荧光定量PCR方法采用的引物的核苷酸序列如SEQ ID NO:3所示和SEQ ID NO:4所示。
3.一种精巢特异蛋白基因,其特征在于,精巢特异蛋白基因的核苷酸序列如SEQ IDNO:1所示。
4.一种精巢特异蛋白,其特征在于,精巢特异蛋白的氨基酸序列如SEQ ID NO:2所示。
5.精巢特异蛋白基因的表达水平在评价昆虫种群质量中的应用,其特征在于,精巢特异蛋白基因的核苷酸序列如SEQ ID NO:1所示;昆虫为大草蛉。
6.根据权利要求5所述应用,其特征在于,精巢特异蛋白基因的核苷酸序列如SEQ IDNO:1所示;和/或精巢特异蛋白基因编码的蛋白质的氨基酸序列如SEQ ID NO:2。
7.用于检测精巢特异蛋白基因的表达水平的物质在评价昆虫种群质量中的应用,其特征在于,精巢特异蛋白基因的核苷酸序列如SEQ ID NO:1所示;昆虫为大草蛉;所述物质为试剂,试剂包括引物,引物的核苷酸序列如SEQ ID NO:3所示和SEQ ID NO:4所示。
CN202111337551.3A 2021-11-10 2021-11-10 一种用精巢特异蛋白基因评价昆虫种群质量的方法 Active CN113957156B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111337551.3A CN113957156B (zh) 2021-11-10 2021-11-10 一种用精巢特异蛋白基因评价昆虫种群质量的方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111337551.3A CN113957156B (zh) 2021-11-10 2021-11-10 一种用精巢特异蛋白基因评价昆虫种群质量的方法

Publications (2)

Publication Number Publication Date
CN113957156A CN113957156A (zh) 2022-01-21
CN113957156B true CN113957156B (zh) 2023-10-13

Family

ID=79470215

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111337551.3A Active CN113957156B (zh) 2021-11-10 2021-11-10 一种用精巢特异蛋白基因评价昆虫种群质量的方法

Country Status (1)

Country Link
CN (1) CN113957156B (zh)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108251535A (zh) * 2018-01-15 2018-07-06 中国农业科学院植物保护研究所 一种用保幼激素基因检测昆虫产卵量的应用及方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108251535A (zh) * 2018-01-15 2018-07-06 中国农业科学院植物保护研究所 一种用保幼激素基因检测昆虫产卵量的应用及方法

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
GenBank: ON125909.1;Liu,X.;Genbank;1-4页 *
大草蛉雄虫卵黄蛋白功能研究;冯彦姣;中国优秀硕士学位论文全文数据库农业科技辑(第1期);D043-301 *

Also Published As

Publication number Publication date
CN113957156A (zh) 2022-01-21

Similar Documents

Publication Publication Date Title
CN109734798B (zh) 飞蝗丝氨酸蛋白酶抑制剂7及其编码基因与应用
CN108610427B (zh) 飞蝗滞育激素基因及其在调控昆虫滞育中的应用
CN109161550A (zh) 一种调控番茄果实抗坏血酸含量的SlbHLH59基因及应用方法
CN112575000B (zh) 青虾sdhb基因及其编码的蛋白和应用
CN110042167A (zh) 热激蛋白基因作为分子标记物检测昆虫温度耐受性的方法
CN109680072A (zh) 检测猪肌内脂肪含量的分子标志物及应用
CN113957156B (zh) 一种用精巢特异蛋白基因评价昆虫种群质量的方法
CN111763252B (zh) 烟粉虱MED隐种染色质重塑因子Btbrm2及其编码基因和应用
CN109734789B (zh) 飞蝗fk506结合蛋白46及其编码基因与应用
CN106471008A (zh) 棕榈Mantle表型检测
CN112048506A (zh) BmKRP基因的dsRNA及其在害虫防治中的应用
CN116463374A (zh) GhSTP18基因在调控植物耐盐性中的应用
CN110106175B (zh) 一种dsRNA及其在害虫防治中的应用
CN114058618B (zh) 谷氨酸脱氢酶作为靶点在防治害虫中的应用
CN107384939B (zh) MtUNUSUAL FLORAL ORGANS基因在调控小叶数量和叶茎比中的应用
CN108753926B (zh) 一种猪背部脂肪厚度的分子标记方法
CN111378670A (zh) 一种分离的中黑盲蝽Taiman基因及其编码的蛋白
CN113373252B (zh) 大豆低硫胁迫特异响应基因、检测引物及其在大豆低硫养分胁迫诊断中的应用
CN114107335B (zh) 泥鳅cdk1基因及其在不育多倍体泥鳅分子育种中的应用
CN109810993B (zh) 一种蝗虫β-D-葡萄糖苷水解酶基因及其应用
CN108610426B (zh) 飞蝗节律基因clk、cyc和per及其在调控昆虫滞育中的应用
CN111321150B (zh) 一种LvCTL4基因及编码的蛋白质、蛋白质的获取方法、表达载体、重组菌和应用
CN109438565B (zh) 飞蝗叉头转录因子LmFoxO及其编码基因与应用
NL2030574B1 (en) Differentially expressed genes (degs) of paeonia ostii waterlogging tolerance and mining method based on rna sequencing (rna-seq)
CN115261502B (zh) 抗赤霉病小麦-纤毛鹅观草4bs·4bl-7sl易位系及选育方法、分子标记和用途

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant