CN110714010B - 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA - Google Patents

一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA Download PDF

Info

Publication number
CN110714010B
CN110714010B CN201911186091.1A CN201911186091A CN110714010B CN 110714010 B CN110714010 B CN 110714010B CN 201911186091 A CN201911186091 A CN 201911186091A CN 110714010 B CN110714010 B CN 110714010B
Authority
CN
China
Prior art keywords
rice
gene
waxy
ala
gly
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
CN201911186091.1A
Other languages
English (en)
Other versions
CN110714010A (zh
Inventor
杨远柱
周延彪
赵新辉
唐倩莹
唐晓丹
廖雪
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.)
Hunan Ava Seeds Co ltd
Hunan Longping Gaoke Seed Science Research Institute Co ltd
Yuan Longping High Tech Agriculture Co ltd
Original Assignee
Hunan Ava Seeds Co ltd
Hunan Longping Gaoke Seed Science Research Institute Co ltd
Yuan Longping High Tech Agriculture Co ltd
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 Hunan Ava Seeds Co ltd, Hunan Longping Gaoke Seed Science Research Institute Co ltd, Yuan Longping High Tech Agriculture Co ltd filed Critical Hunan Ava Seeds Co ltd
Priority to CN201911186091.1A priority Critical patent/CN110714010B/zh
Publication of CN110714010A publication Critical patent/CN110714010A/zh
Application granted granted Critical
Publication of CN110714010B publication Critical patent/CN110714010B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/415Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8216Methods for controlling, regulating or enhancing expression of transgenes in plant cells
    • C12N15/8218Antisense, co-suppression, viral induced gene silencing [VIGS], post-transcriptional induced gene silencing [PTGS]
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8242Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
    • C12N15/8243Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine
    • C12N15/8245Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine involving modified carbohydrate or sugar alcohol metabolism, e.g. starch biosynthesis
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/20Type of nucleic acid involving clustered regularly interspaced short palindromic repeats [CRISPRs]

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Microbiology (AREA)
  • Plant Pathology (AREA)
  • Cell Biology (AREA)
  • Nutrition Science (AREA)
  • Botany (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Virology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)

Abstract

本发明公开了一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA,属于生物技术领域,包括如下步骤:抑制水稻中所述Waxy基因的表达;所述Waxy基因为编码Waxy蛋白的基因。本发明利用CRISPR/Cas9技术,定点编辑水稻Waxy基因,通过造成移码突变,敲除了水稻Waxy基因,获得了直链淀粉含量明显降低的新一代水稻新种质。获得的Waxy定点编辑株系与野生型相比,直链淀粉含量均显著降低。

Description

一种通过基因编辑降低水稻直链淀粉含量的方法及其专用 sgRNA
技术领域
本发明属于生物技术领域,涉及一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA。
背景技术
稻米胚乳的主要成分是淀粉,一般占米粉干重的76%,以不规则多角形颗粒状存在胚乳中。淀粉分为直链淀粉(Amylose)和支链淀粉(Amylopectin)两类,均是由葡萄糖结合而成的多糖物质,并且包被少量的脂肪和蛋白。糯稻中直链淀粉含量低于2%,非糯性粳稻品种直链淀粉含量一般低于籼稻品种。
水稻胚乳中的直链淀粉主要由水稻蜡质基因(Waxy)编码的颗粒结合淀粉合成酶(granule bound starch synthaseⅠ,GBSSⅠ)催化合成,是控制直链淀粉合成的主效基因。国内外对Wx基因的结构和功能已进行了广泛的研究。水稻Wx基因由Wang等(1990)成功克隆,Wx基因位于水稻第6号染色体短臂上,共含有14个外显子和13个内含子,全长6185bp,编码的GBSSⅠ蛋白含有609个氨基酸。该基因基因具有较长的第1内含子,且内含子内有增强基因表达的功能。
直链淀粉是由α-1,4糖苷键连接成的数千单位长的、极少分支的多聚葡萄糖链状线性分子。直链淀粉占总淀粉含量的0~30%,含有很少量的分支结构。一般而言,直链淀粉主要以单螺旋或随机缠绕的方式分布在淀粉颗粒的无定形层中。直链淀粉能溶于水,但不稳定。支链淀粉是由α-1,4糖苷键相连的葡萄糖链和分支点上α-1,6糖苷键共同连接成的高度分支的多聚合体,一般占总淀粉含量的70%以上。支链淀粉每个分子上大约含有220-1050个分支,每个分支链长一般为12dp-60dp。支链淀粉主要以螺旋结构存在于淀粉粒的晶体片层中,不易被酶水解。直链淀粉含量(Amylose content,AC)为直链淀粉占精米粉干重的百分比,是决定稻米蒸煮与食味品质的关键因素之一。根据其含量高低,可将稻米直链淀粉含量分为极低(2%~9%)、低(10%~20%)、中(20%~25%)和高(>25%)四类,糯稻直链淀粉含量一般低于2%。稻米胚乳中直链淀粉含量能影响蒸煮后米饭柔软性,直链淀粉含量过低,膨胀性小,米饭粘;直链淀粉含量过高,膨胀性大,变冷后质地较硬;中等直链淀粉含量的稻米煮后比较松软,蒸煮品质相对好。
近年来,水稻生产模式和消费取向正在不断进行适应性调整,水稻生产已从以单一的数量型增长为目标转变为以数量和质量并重为目标,高营养、高品质的功能型稻米越来越受到人们喜爱。糯米和糯米制品的市场需求也逐渐扩大,人们对糯稻资源的利用研究和糯米产品的开发利用也不断加强,以糯米为原料,研制开发各种滋补、保健特色食品和饮料供应市场,深受消费者的欢迎,并获得显著的经济效益。糯米虽不适宜作为主食长期食用,但它是酿造、节日食品(如粽子等)、糕点制作以及许多传统副食品(如八宝粥等)生产的主要原料,也是食品加工业的重要原料,因而有着广泛而重要的用途。同时糯米富含蛋白质和脂肪,营养价值较高。它还是东南亚某些地区的人们喜爱的传统食粮。因此,在当前粮食种植结构调整优化的新时期,糯稻的研究和利用尤为重要。
随着CRISPR/Cas9技术在人类与动物细胞系中建立并应用,经过改造的CRISPR/Cas9系统也迅速地被应用到水稻、玉米、小麦和高粱等不同作物基因组的定向编辑研究中,并且获得较高的诱导突变率和可稳定遗传的基因组编辑植株,为作物的快速育种提供了一条新的途径。
发明内容
本发明的目的在于提供一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA。其具体技术方案为:
一种通过基因编辑降低水稻种子直链淀粉含量的方法,包括以下步骤:
抑制水稻中Waxy基因的表达;所述Waxy基因为编码Waxy蛋白的基因。
所述Waxy蛋白为如下(1)或(2):(1)由SEQ:ID:NO:3所示的氨基酸序列组成的蛋白质;(2)将序列3的氨基酸序列经过一个至十个氨基酸残基的取代和/或缺失和/或添加且具有相同功能的其衍生的蛋白质。
所述Waxy基因为如下(1)或(2)或(3)或(4)的DNA序列:(1)由SEQ:ID:NO:1和由SEQ:ID:NO:2所示的DNA序列;(2)编码序列表中由SEQ:ID:NO:3所示的蛋白质序列的多核苷酸;(3)在严格条件下可与序列表中序列1和序列2限定的DNA序列杂交且编码所述Waxy蛋白的DNA序列;(4)与序列表中序列1和序列2限定的DNA序列至少具有90%以上同源性,且编码所述Waxy蛋白的DNA序列。
所述抑制水稻Waxy基因的表达是通过对水稻Waxy基因进行基因编辑实现的。所述基因编辑是通过CRISPR/Cas9系统实现的。所述CRISPR/Cas9系统中,sgRNA的靶标序列如下:ATCCACAACATCTCCTACCA。所述sgRNA的编码基因如SEQ:ID:NO:5所示。
所述抑制水稻中Waxy基因的表达是通过在水稻中导入含有Cas9蛋白的编码基因和sgRNA的编码基因的特异DNA分子实现的。所述抑制水稻中Waxy基因的表达是通过在水稻中导入含有Cas9蛋白的编码基因的DNA分子和含有sgRNA的编码基因的DNA分子实现的。所述sgRNA的编码基因如序列表的由SEQ:ID:NO:4核苷酸所示。所述Cas9蛋白的编码基因具体可为序列表的由SEQ:ID:NO:5核苷酸所示。
所述水稻具体可为水稻品种638S和华占。
本发明还保护一种特异sgRNA,其靶标序列如下:ATCCACAACATCTCCTACCA。所述sgRNA的编码基因如序列表的由SEQ:ID:NO:4核苷酸所示。
还包括如下步骤:抑制水稻中所述Waxy蛋白的活性。所述水稻具体可为水稻品种638S和华占。
本发明还保护一种抑制水稻中Waxy基因的表达的方法,包括如下步骤:借助CRISPR/Cas9系统通过对水稻Waxy基因进行基因编辑从而抑制水稻Waxy基因的表达。所述CRISPR/Cas9系统中,sgRNA的靶标序列如下:ATCCACAACATCTCCTACCA。所述水稻具体可为水稻品种638S和华占。
本发明利用CRISPR/Cas9技术,定点编辑水稻Waxy基因,通过造成移码突变,敲除了水稻Waxy基因,获得了直链淀粉含量明显降低的新一代水稻新种质。获得的Waxy定点编辑株系与野生型相比,直链淀粉含量均显著降低。
附图说明
图1 Waxy基因的CRISPR/Cas9载体构建。A:Waxy基因的靶点及CRISPR/Cas9载体构建;B:农杆菌的PCR检测。
图2 T0代waxy突变体的纯合突变类型;
图3 waxy突变体的稻米表型和直链淀粉含量。A:638S-waxy的稻米表型;B:638S-waxy的直链淀粉含量;C:华占-waxy的稻米表型;D:华占-waxy的直链淀粉含量。
具体实施方式
下面结合附图和实施例对本发明的技术方案作进一步详细地说明。
下述实施例中所用的材料、试剂等,如无特殊说明,均可从商业途径得到。
1.基因编辑载体的构建
为了获得638S和华占直链淀粉含量降低的植株,根据CRISPR/Cas9系统识别特点设计靶位点,在Waxy基因的第7外显子区域设计20bp的sgRNA靶点序列ATCCACAACATCTCCTACCA,PAM序列GGG位于靶序列3’末端,通过KpnI和HindIII双酶切方式构建CRISPR/Cas9重组载体(图1A),重组载体经电击转化农杆菌EHA105。利用重组载体上的GUS报告基因,设计特异性检测正向引物GUS-F:5'CGTCCGTCCTGTAGAAACCC 3'和反向引物GUS-R:5'GTGCGGATTCACCACTTGC 3'进行农杆菌菌液检测,扩增产物大小为718bp,能扩增出目的片段大小的菌液为阳性菌株(图1B)。
2.水稻转化
将检测有目的条带的阳性农杆菌侵染638S和华占成熟胚的愈伤组织,将浸染后的愈伤组织共培养3天(避光,28℃),再经过含有50mg/L潮霉素的筛选培养基上进行抗性愈伤的筛选以及分化培养基分化出T0代抗性幼苗,然后将分化出的水稻植株在阴凉处水培炼苗1周,用于转基因检测。
3.转基因植株的获得及突变位点分析
通过载体上特异性引物GUS-F/GUS-R对T0代组培苗进行PCR检测,筛选阳性转基因植株。为了检测阳性转基因植株的靶位点突变情况,在Waxy基因靶点两端分别设计测序引物Wx-CX-F:5'CCTAAACCTCAACAACAACCCAT 3'和Wx-CX-R:5'CGTGGTTGCGTCGTACTTGG 3'。通过PCR扩增目的片段送测序公司测序,分析突变类型。638S和华占的waxy基因纯合突变类型如图2所示。638S的waxy突变体命名为638S-waxy和华占的waxy突变体命名为华占-waxy,它们在靶位点都有单碱基A的插入,使mRNA移码导致翻译提前终止。
4.直链淀粉含量的检测
将638S-waxy和华占-waxy纯合突变类型的植株移栽大田,直至成熟收种。种子去壳打成精米观察稻米外形。638S-waxy和华占-waxy稻米的粒形与对照相比无显著差异,但是638S-waxy和华占-waxy的稻米呈现乳白色,典型的糯米特征(图3A,C)。进一步对638S-waxy和华占-waxy的稻米进行直链淀粉含量的测定。通过检测,638S-waxy和华占-waxy稻米的直链淀粉含量分别为1.6%和1.8%,而对照638S和华占的直链淀粉含量分别为13.0%和13.6%(图3B,D)。结果说明,通过CRISPR/Cas9基因编辑技术敲除Waxy基因后,突变体植株的种子直链淀粉含量显著低于对照品种。
以上所述,仅为本发明较佳的具体实施方式,本发明的保护范围不限于此,任何熟悉本技术领域的技术人员在本发明披露的技术范围内,可显而易见地得到的技术方案的简单变化或等效替换均落入本发明的保护范围内。
序列表
<110> 袁隆平农业高科技股份有限公司
湖南亚华种业科学研究院
湖南隆平高科种业科学研究院有限公司
<120> 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA
<160> 5
<170> SIPOSequenceListing 1.0
<210> 1
<211> 5035
<212> DNA
<213> 水稻属水稻(Oryza sativa L.)
<400> 1
accattcctt cagttctttg tctatctcaa gacacaaata actgcagtct ctctctctct 60
ctctctctct ctctctctct ctctgcttca cttctctgct tgtgttgttc tgttgttcat 120
caggaagaac atctgcaagt tatacatata tgtttataat tctttgtttc ccctcttatt 180
cagatcgatc acatgcatct ttcattgctc gtttttcctt acaagtagtc tcatacatgc 240
taatttctgt aaggtgttgg gctggaaatt aattaattaa ttaattgact tgccaagatc 300
catatatatg tcctgatatt aaatcttcgt tcgttatgtt tggttaggct gatcaatgtt 360
attctagagt ctagagaaac acacccaggg gttttccaac tagctccaca agatggtggg 420
ctagctgacc tagatttgaa gtctcactcc ttataattat tttatattag atcattttct 480
aatattcgtg tcttttttta ttctagagtc tagatcttgt gttcaactct cgttaaatca 540
tgtctctcgc cactggagaa acagatcagg agggtttatt ttgggtatag gtcaaagcta 600
agattgaaat tcacaaatag taaaatcaga atccaaccaa ttttagtagc cgagttggtc 660
aaaggaaaat gtatatagct agatttattg ttttggcaaa aaaaaatctg aatatgcaaa 720
atacttgtat atctttgtat taagaagatg aaaataagta gcagaaaatt aaaaaatgga 780
ttatatttcc tgggctaaaa gaattgttga tttggcacaa ttaaattcag tgtcaaggtt 840
ttgtgcaaga attcagtgtg aaggaataga ttctcttcaa aacaatttaa tcattcatct 900
gatctgctca aagctctgtg catctccggg tgcaacggcc aggatattta ttgtgcagta 960
aaaaaatgtc atatccccta gccacccaag aaactgctcc ttaagtcctt ataagcacat 1020
atggcattgt aatatatatg tttgagtttt agcgacaatt tttttaaaaa cttttggtcc 1080
tttttatgaa cgttttaagt ttcactgtct ttttttttcg aattttaaat gtagcttcaa 1140
attctaatcc ccaatccaaa ttgtaataaa cttcaattct cctaattaac atcttaattc 1200
atttatttga aaaccagttc aaattctttt aggctcacca aaccttaaac aattcaattc 1260
agtgcagaga tcttccacag caacagctag acaaccacca tgtcggctct caccacgtcc 1320
cagctcgcca cctcggccac cggcttcggc atcgccgaca ggtcggcgcc gtcgtcgctg 1380
ctccgccacg ggttccaggg cctcaagccc cgcagccccg ccggcggcga cgcgacgtcg 1440
ctcagcgtga cgaccagcgc gcgcgcgacg cccaagcagc agcggtcggt gcagcgtggc 1500
agccggaggt tcccctccgt cgtcgtgtac gccaccggcg ccggcatgaa cgtcgtgttc 1560
gtcggcgccg agatggcccc ctggagcaag accggcggcc tcggtgacgt cctcggtggc 1620
ctcccccctg ccatggctgt aagcacacac aaacttcgat cgctcgtcgt cgctgaccgt 1680
cgtcgtcttc aactgttctt gatcatcgca ttggatggat gtgtaatgtt gtgttcttgt 1740
gttctttgca ggcgaatggc cacagggtca tggtgatctc tcctcggtac gaccagtaca 1800
aggacgcttg ggataccagc gttgtggctg aggtaggagc atatgcgtga tcagatcatc 1860
acaagatcga ttagctttag atgatttgtt acatttcgca agattttaac ccaagttttt 1920
gtggtgcaat tcattgcaga tcaaggttgc agacaggtac gagagggtga ggtttttcca 1980
ttgctacaag cgtggagtcg accgtgtgtt catcgaccat ccgtcattcc tggagaaggt 2040
ggagtcatca ttagtttacc ttttttgttt ttactgaatt attaacagtg catttagcag 2100
ttggactgag cttagcttcc actggtgatt tcaggtttgg ggaaagaccg gtgagaagat 2160
ctacggacct gacactggag ttgattacaa agacaaccag atgcgtttca gccttctttg 2220
ccaggtcagt gattacttct atctgatgat ggttggaagc atcacgagtt taccatagta 2280
tgtatggatt cataactaat tcgtgtattg atgctacctg caggcagcac tcgaggctcc 2340
taggatccta aacctcaaca acaacccata cttcaaagga acttatggtg agttacaatt 2400
gatctcaaga tcttataact ttcttcgaag gaatccatga tgatcagact aattccttcc 2460
ggtttgttac tgacaacagg tgaggatgtt gtgttcgtct gcaacgactg gcacactggc 2520
ccactggcga gctacctgaa gaacaactac cagcccaatg gcatctacag gaatgcaaag 2580
gtctatgctt gttcttgcca taccaactca aatctgcatg cacactgcat tctgttcaga 2640
aactgactgt ctgaatcttt ttcactgcag gttgctttct gcatccacaa catctcctac 2700
cagggccgtt tcgctttcga ggattaccct gagctgaacc tctccgagag gttcaggtca 2760
tccttcgatt tcatcgacgg gtatgagtaa gattctaaga gtaacttact gtcaattcgc 2820
catatatcga ttcaatccaa gatccttttg agctgacaac cctgcactac tgtccatcgt 2880
tcaaatccgg ttaaatttca ggtatgacac gccggtggag ggcaggaaga tcaactggat 2940
gaaggccgga atcctggaag ccgacagggt gctcaccgtg agcccgtact acgccgagga 3000
gctcatctcc ggcatcgcca ggggatgcga gctcgacaac atcatgcggc tcaccggcat 3060
caccggcatc gtcaacggca tggacgtcag cgagtgggat cctagcaagg acaagtacat 3120
caccgccaag tacgacgcaa ccacggtaag aacgaatgca ttcttcacaa gatatgcaat 3180
ctgaattttc tttgaaaaag aaattatcat ctgtcacttc ttgattgatt ctgacaaggc 3240
aagaatgagt gacaaatttc aggcaatcga ggcgaaggcg ctgaacaagg aggcgttgca 3300
ggcggaggcg ggtcttccgg tcgacaggaa aatcccactg atcgcgttca tcggcaggct 3360
ggaggaacag aagggccctg acgtcatggc cgccgccatc ccggagctca tgcaggagga 3420
cgtccagatc gttcttctgg tataatataa tacactacaa gacacacttg cacgatatgc 3480
caaaaattca gaacaaattc agtggcaaaa aaaaaactcg aatattaggg aaggacctaa 3540
taatatcaaa taattagaag gggtgaggct ttgaacccag atcgtctagt ccaccacctt 3600
gtggagttag ccggaagacc tctgagcatt tctcaattca gtggcaaatg atgtgtataa 3660
ttttgatccg tgtgtgtttc agggtactgg aaagaagaag ttcgagaagc tgctcaagag 3720
catggaggag aagtatccgg gcaaggtgag ggccgtggtg aagttcaacg cgccgcttgc 3780
tcatctcatc atggccggag ccgacgtgct cgccgtcccc agccgcttcg agccctgtgg 3840
actcatccag ctgcagggga tgagatacgg aacggtatac aatttccatc tatcaattcg 3900
attgttcgat ttcatctttg tgcaatgcaa tgcaattgca aatgcaaatg catgatgatt 3960
ttccttgttg atttctccag ccctgtgctt gcgcgtccac cggtgggctc gtggacacgg 4020
tcatcgaagg caagactggt ttccacatgg gccgtctcag cgtcgacgta agcctataca 4080
tttacataac aatcagatat gacacatcct aataccgata agtcggtaca ctactacaca 4140
tttacatggt tgctggttat atggtttttt tggcagtgca aggtggtgga gccaagcgac 4200
gtgaagaagg tggcggccac cctgaagcgc gccatcaagg tcgtcggcac gccggcgtac 4260
gaggagatgg tcaggaactg catgaaccag gacctctcct ggaaggtata aattacgaaa 4320
caaatttaac ccaaacatat actatatact ccctccgctt ctaaatattc aacgccgttg 4380
tcttttttaa atatgtttga ccattcgtct tattaaaaaa attaaataat tataaattct 4440
tttcctatca tttgattcat tgttaaatat acttatatgt atacatatag ttttacatat 4500
ttcataaaat tttttgaaca agacgaacgg tcaaacatgt gctaaaaagt taacggtgtc 4560
gaatattcag aaacggaggg agtataaacg tcttgttcag aagttcagag attcacctgt 4620
ctgatgctga tgatgattaa ttgtttgcaa catggatttc aggggcctgc gaagaactgg 4680
gagaatgtgc tcctgggcct gggcgtcgcc ggcagcgcgc cggggatcga aggcgacgag 4740
atcgcgccgc tcgccaagga gaacgtggct gctccttgaa gagcctgaga tctacatatg 4800
gagtgattaa ttaatatagc agtatatgga tgagagacga atgaaccagt ggtttgtttg 4860
ttgtagtgaa tttgtagcta tagccaatta tataggctaa taagtttgat gttgtactct 4920
tctgggtgtg cttaagtatc ttatcggacc ctgaatttat gtgtgtggct tattgccaat 4980
aatattaagt aataaagggt ttattatatt attatatatg ttatattata cttcc 5035
<210> 2
<211> 1830
<212> DNA
<213> 水稻属水稻(Oryza sativa L.)
<400> 2
atgtcggctc tcaccacgtc ccagctcgcc acctcggcca ccggcttcgg catcgccgac 60
aggtcggcgc cgtcgtcgct gctccgccac gggttccagg gcctcaagcc ccgcagcccc 120
gccggcggcg acgcgacgtc gctcagcgtg acgaccagcg cgcgcgcgac gcccaagcag 180
cagcggtcgg tgcagcgtgg cagccggagg ttcccctccg tcgtcgtgta cgccaccggc 240
gccggcatga acgtcgtgtt cgtcggcgcc gagatggccc cctggagcaa gaccggcggc 300
ctcggtgacg tcctcggtgg cctcccccct gccatggctg cgaatggcca cagggtcatg 360
gtgatctctc ctcggtacga ccagtacaag gacgcttggg ataccagcgt tgtggctgag 420
atcaaggttg cagacaggta cgagagggtg aggtttttcc attgctacaa gcgtggagtc 480
gaccgtgtgt tcatcgacca tccgtcattc ctggagaagg tttggggaaa gaccggtgag 540
aagatctacg gacctgacac tggagttgat tacaaagaca accagatgcg tttcagcctt 600
ctttgccagg cagcactcga ggctcctagg atcctaaacc tcaacaacaa cccatacttc 660
aaaggaactt atggtgagga tgttgtgttc gtctgcaacg actggcacac tggcccactg 720
gcgagctacc tgaagaacaa ctaccagccc aatggcatct acaggaatgc aaaggttgct 780
ttctgcatcc acaacatctc ctaccagggc cgtttcgctt tcgaggatta ccctgagctg 840
aacctctccg agaggttcag gtcatccttc gatttcatcg acgggtatga cacgccggtg 900
gagggcagga agatcaactg gatgaaggcc ggaatcctgg aagccgacag ggtgctcacc 960
gtgagcccgt actacgccga ggagctcatc tccggcatcg ccaggggatg cgagctcgac 1020
aacatcatgc ggctcaccgg catcaccggc atcgtcaacg gcatggacgt cagcgagtgg 1080
gatcctagca aggacaagta catcaccgcc aagtacgacg caaccacggc aatcgaggcg 1140
aaggcgctga acaaggaggc gttgcaggcg gaggcgggtc ttccggtcga caggaaaatc 1200
ccactgatcg cgttcatcgg caggctggag gaacagaagg gccctgacgt catggccgcc 1260
gccatcccgg agctcatgca ggaggacgtc cagatcgttc ttctgggtac tggaaagaag 1320
aagttcgaga agctgctcaa gagcatggag gagaagtatc cgggcaaggt gagggccgtg 1380
gtgaagttca acgcgccgct tgctcatctc atcatggccg gagccgacgt gctcgccgtc 1440
cccagccgct tcgagccctg tggactcatc cagctgcagg ggatgagata cggaacgccc 1500
tgtgcttgcg cgtccaccgg tgggctcgtg gacacggtca tcgaaggcaa gactggtttc 1560
cacatgggcc gtctcagcgt cgactgcaag gtggtggagc caagcgacgt gaagaaggtg 1620
gcggccaccc tgaagcgcgc catcaaggtc gtcggcacgc cggcgtacga ggagatggtc 1680
aggaactgca tgaaccagga cctctcctgg aaggggcctg cgaagaactg ggagaatgtg 1740
ctcctgggcc tgggcgtcgc cggcagcgcg ccggggatcg aaggcgacga gatcgcgccg 1800
ctcgccaagg agaacgtggc tgctccttga 1830
<210> 3
<211> 609
<212> PRT
<213> 水稻属水稻(Oryza sativa L.)
<400> 3
Met Ser Ala Leu Thr Thr Ser Gln Leu Ala Thr Ser Ala Thr Gly Phe
1 5 10 15
Gly Ile Ala Asp Arg Ser Ala Pro Ser Ser Leu Leu Arg His Gly Phe
20 25 30
Gln Gly Leu Lys Pro Arg Ser Pro Ala Gly Gly Asp Ala Thr Ser Leu
35 40 45
Ser Val Thr Thr Ser Ala Arg Ala Thr Pro Lys Gln Gln Arg Ser Val
50 55 60
Gln Arg Gly Ser Arg Arg Phe Pro Ser Val Val Val Tyr Ala Thr Gly
65 70 75 80
Ala Gly Met Asn Val Val Phe Val Gly Ala Glu Met Ala Pro Trp Ser
85 90 95
Lys Thr Gly Gly Leu Gly Asp Val Leu Gly Gly Leu Pro Pro Ala Met
100 105 110
Ala Ala Asn Gly His Arg Val Met Val Ile Ser Pro Arg Tyr Asp Gln
115 120 125
Tyr Lys Asp Ala Trp Asp Thr Ser Val Val Ala Glu Ile Lys Val Ala
130 135 140
Asp Arg Tyr Glu Arg Val Arg Phe Phe His Cys Tyr Lys Arg Gly Val
145 150 155 160
Asp Arg Val Phe Ile Asp His Pro Ser Phe Leu Glu Lys Val Trp Gly
165 170 175
Lys Thr Gly Glu Lys Ile Tyr Gly Pro Asp Thr Gly Val Asp Tyr Lys
180 185 190
Asp Asn Gln Met Arg Phe Ser Leu Leu Cys Gln Ala Ala Leu Glu Ala
195 200 205
Pro Arg Ile Leu Asn Leu Asn Asn Asn Pro Tyr Phe Lys Gly Thr Tyr
210 215 220
Gly Glu Asp Val Val Phe Val Cys Asn Asp Trp His Thr Gly Pro Leu
225 230 235 240
Ala Ser Tyr Leu Lys Asn Asn Tyr Gln Pro Asn Gly Ile Tyr Arg Asn
245 250 255
Ala Lys Val Ala Phe Cys Ile His Asn Ile Ser Tyr Gln Gly Arg Phe
260 265 270
Ala Phe Glu Asp Tyr Pro Glu Leu Asn Leu Ser Glu Arg Phe Arg Ser
275 280 285
Ser Phe Asp Phe Ile Asp Gly Tyr Asp Thr Pro Val Glu Gly Arg Lys
290 295 300
Ile Asn Trp Met Lys Ala Gly Ile Leu Glu Ala Asp Arg Val Leu Thr
305 310 315 320
Val Ser Pro Tyr Tyr Ala Glu Glu Leu Ile Ser Gly Ile Ala Arg Gly
325 330 335
Cys Glu Leu Asp Asn Ile Met Arg Leu Thr Gly Ile Thr Gly Ile Val
340 345 350
Asn Gly Met Asp Val Ser Glu Trp Asp Pro Ser Lys Asp Lys Tyr Ile
355 360 365
Thr Ala Lys Tyr Asp Ala Thr Thr Ala Ile Glu Ala Lys Ala Leu Asn
370 375 380
Lys Glu Ala Leu Gln Ala Glu Ala Gly Leu Pro Val Asp Arg Lys Ile
385 390 395 400
Pro Leu Ile Ala Phe Ile Gly Arg Leu Glu Glu Gln Lys Gly Pro Asp
405 410 415
Val Met Ala Ala Ala Ile Pro Glu Leu Met Gln Glu Asp Val Gln Ile
420 425 430
Val Leu Leu Gly Thr Gly Lys Lys Lys Phe Glu Lys Leu Leu Lys Ser
435 440 445
Met Glu Glu Lys Tyr Pro Gly Lys Val Arg Ala Val Val Lys Phe Asn
450 455 460
Ala Pro Leu Ala His Leu Ile Met Ala Gly Ala Asp Val Leu Ala Val
465 470 475 480
Pro Ser Arg Phe Glu Pro Cys Gly Leu Ile Gln Leu Gln Gly Met Arg
485 490 495
Tyr Gly Thr Pro Cys Ala Cys Ala Ser Thr Gly Gly Leu Val Asp Thr
500 505 510
Val Ile Glu Gly Lys Thr Gly Phe His Met Gly Arg Leu Ser Val Asp
515 520 525
Cys Lys Val Val Glu Pro Ser Asp Val Lys Lys Val Ala Ala Thr Leu
530 535 540
Lys Arg Ala Ile Lys Val Val Gly Thr Pro Ala Tyr Glu Glu Met Val
545 550 555 560
Arg Asn Cys Met Asn Gln Asp Leu Ser Trp Lys Gly Pro Ala Lys Asn
565 570 575
Trp Glu Asn Val Leu Leu Gly Leu Gly Val Ala Gly Ser Ala Pro Gly
580 585 590
Ile Glu Gly Asp Glu Ile Ala Pro Leu Ala Lys Glu Asn Val Ala Ala
595 600 605
Pro
<210> 4
<211> 94
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 4
gggtcttcga gaagacctgt tttagagcta gaaatagcaa gttaaaataa ggctagtccg 60
ttatcaactt gaaaaagtgg caccgagtcg gtgc 94
<210> 5
<211> 4101
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 5
gacaagaagt acagcatcgg cctggacatc ggcaccaact ctgtgggctg ggccgtgatc 60
accgacgagt acaaggtgcc cagcaagaaa ttcaaggtgc tgggcaacac cgaccggcac 120
agcatcaaga agaacctgat cggagccctg ctgttcgaca gcggcgaaac agccgaggcc 180
acccggctga agagaaccgc cagaagaaga tacaccagac ggaagaaccg gatctgctat 240
ctgcaagaga tcttcagcaa cgagatggcc aaggtggacg acagcttctt ccacagactg 300
gaagagtcct tcctggtgga agaggataag aagcacgagc ggcaccccat cttcggcaac 360
atcgtggacg aggtggccta ccacgagaag taccccacca tctaccacct gagaaagaaa 420
ctggtggaca gcaccgacaa ggccgacctg cggctgatct atctggccct ggcccacatg 480
atcaagttcc ggggccactt cctgatcgag ggcgacctga accccgacaa cagcgacgtg 540
gacaagctgt tcatccagct ggtgcagacc tacaaccagc tgttcgagga aaaccccatc 600
aacgccagcg gcgtggacgc caaggccatc ctgtctgcca gactgagcaa gagcagacgg 660
ctggaaaatc tgatcgccca gctgcccggc gagaagaaga atggcctgtt cggcaacctg 720
attgccctga gcctgggcct gacccccaac ttcaagagca acttcgacct ggccgaggat 780
gccaaactgc agctgagcaa ggacacctac gacgacgacc tggacaacct gctggcccag 840
atcggcgacc agtacgccga cctgtttctg gccgccaaga acctgtccga cgccatcctg 900
ctgagcgaca tcctgagagt gaacaccgag atcaccaagg cccccctgag cgcctctatg 960
atcaagagat acgacgagca ccaccaggac ctgaccctgc tgaaagctct cgtgcggcag 1020
cagctgcctg agaagtacaa agagattttc ttcgaccaga gcaagaacgg ctacgccggc 1080
tacattgacg gcggagccag ccaggaagag ttctacaagt tcatcaagcc catcctggaa 1140
aagatggacg gcaccgagga actgctcgtg aagctgaaca gagaggacct gctgcggaag 1200
cagcggacct tcgacaacgg cagcatcccc caccagatcc acctgggaga gctgcacgcc 1260
attctgcggc ggcaggaaga tttttaccca ttcctgaagg acaaccggga aaagatcgag 1320
aagatcctga ccttccgcat cccctactac gtgggccctc tggccagggg aaacagcaga 1380
ttcgcctgga tgaccagaaa gagcgaggaa accatcaccc cctggaactt cgaggaagtg 1440
gtggacaagg gcgcttccgc ccagagcttc atcgagcgga tgaccaactt cgataagaac 1500
ctgcccaacg agaaggtgct gcccaagcac agcctgctgt acgagtactt caccgtgtat 1560
aacgagctga ccaaagtgaa atacgtgacc gagggaatga gaaagcccgc cttcctgagc 1620
ggcgagcaga aaaaggccat cgtggacctg ctgttcaaga ccaaccggaa agtgaccgtg 1680
aagcagctga aagaggacta cttcaagaaa atcgagtgct tcgactccgt ggaaatctcc 1740
ggcgtggaag atcggttcaa cgcctccctg ggcacatacc acgatctgct gaaaattatc 1800
aaggacaagg acttcctgga caatgaggaa aacgaggaca ttctggaaga tatcgtgctg 1860
accctgacac tgtttgagga cagagagatg atcgaggaac ggctgaaaac ctatgcccac 1920
ctgttcgacg acaaagtgat gaagcagctg aagcggcgga gatacaccgg ctggggcagg 1980
ctgagccgga agctgatcaa cggcatccgg gacaagcagt ccggcaagac aatcctggat 2040
ttcctgaagt ccgacggctt cgccaacaga aacttcatgc agctgatcca cgacgacagc 2100
ctgaccttta aagaggacat ccagaaagcc caggtgtccg gccagggcga tagcctgcac 2160
gagcacattg ccaatctggc cggcagcccc gccattaaga agggcatcct gcagacagtg 2220
aaggtggtgg acgagctcgt gaaagtgatg ggccggcaca agcccgagaa catcgtgatc 2280
gaaatggcca gagagaacca gaccacccag aagggacaga agaacagccg cgagagaatg 2340
aagcggatcg aagagggcat caaagagctg ggcagccaga tcctgaaaga acaccccgtg 2400
gaaaacaccc agctgcagaa cgagaagctg tacctgtact acctgcagaa tgggcgggat 2460
atgtacgtgg accaggaact ggacatcaac cggctgtccg actacgatgt ggaccatatc 2520
gtgcctcaga gctttctgaa ggacgactcc atcgacaaca aggtgctgac cagaagcgac 2580
aagaaccggg gcaagagcga caacgtgccc tccgaagagg tcgtgaagaa gatgaagaac 2640
tactggcggc agctgctgaa cgccaagctg attacccaga gaaagttcga caatctgacc 2700
aaggccgaga gaggcggcct gagcgaactg gataaggccg gcttcatcaa gagacagctg 2760
gtggaaaccc ggcagatcac aaagcacgtg gcacagatcc tggactcccg gatgaacact 2820
aagtacgacg agaatgacaa gctgatccgg gaagtgaaag tgatcaccct gaagtccaag 2880
ctggtgtccg atttccggaa ggatttccag ttttacaaag tgcgcgagat caacaactac 2940
caccacgccc acgacgccta cctgaacgcc gtcgtgggaa ccgccctgat caaaaagtac 3000
cctaagctgg aaagcgagtt cgtgtacggc gactacaagg tgtacgacgt gcggaagatg 3060
atcgccaaga gcgagcagga aatcggcaag gctaccgcca agtacttctt ctacagcaac 3120
atcatgaact ttttcaagac cgagattacc ctggccaacg gcgagatccg gaagcggcct 3180
ctgatcgaga caaacggcga aaccggggag atcgtgtggg ataagggccg ggattttgcc 3240
accgtgcgga aagtgctgag catgccccaa gtgaatatcg tgaaaaagac cgaggtgcag 3300
acaggcggct tcagcaaaga gtctatcctg cccaagagga acagcgataa gctgatcgcc 3360
agaaagaagg actgggaccc taagaagtac ggcggcttcg acagccccac cgtggcctat 3420
tctgtgctgg tggtggccaa agtggaaaag ggcaagtcca agaaactgaa gagtgtgaaa 3480
gagctgctgg ggatcaccat catggaaaga agcagcttcg agaagaatcc catcgacttt 3540
ctggaagcca agggctacaa agaagtgaaa aaggacctga tcatcaagct gcctaagtac 3600
tccctgttcg agctggaaaa cggccggaag agaatgctgg cctctgccgg cgaactgcag 3660
aagggaaacg aactggccct gccctccaaa tatgtgaact tcctgtacct ggccagccac 3720
tatgagaagc tgaagggctc ccccgaggat aatgagcaga aacagctgtt tgtggaacag 3780
cacaagcact acctggacga gatcatcgag cagatcagcg agttctccaa gagagtgatc 3840
ctggccgacg ctaatctgga caaagtgctg tccgcctaca acaagcaccg ggataagccc 3900
atcagagagc aggccgagaa tatcatccac ctgtttaccc tgaccaatct gggagcccct 3960
gccgccttca agtactttga caccaccatc gaccggaaga ggtacaccag caccaaagag 4020
gtgctggacg ccaccctgat ccaccagagc atcaccggcc tgtacgagac acggatcgac 4080
ctgtctcagc tgggaggcga c 4101

Claims (5)

1.一种通过基因编辑降低水稻直链淀粉含量的方法,其特征在于,包括以下步骤:
抑制水稻中Waxy基因的表达;所述Waxy基因为编码Waxy蛋白的基因,所述Waxy蛋白由序列1所示的DNA序列编码,所述抑制水稻Waxy基因的表达是通过对水稻Waxy基因进行基因编辑实现的;所述基因编辑是通过CRISPR/Cas9系统实现的;所述CRISPR/Cas9系统中,sgRNA的靶标序列如下:ATCCACAACATCTCCTACCA 。
2.根据权利要求1所述的通过基因编辑降低水稻直链淀粉含量的方法,其特征在于,所述抑制水稻中Waxy基因的表达是通过在水稻中导入含有Cas9蛋白的编码基因和sgRNA的编码基因的特异DNA分子实现的;所述抑制水稻中Waxy基因的表达是通过在水稻中导入含有Cas9蛋白的编码基因的DNA分子和含有sgRNA的编码基因的DNA分子实现的;所述sgRNA的编码基因如序列表的由SEQ:ID:NO:4核苷酸所示;所述Cas9蛋白的编码基因具体可为序列表的由SEQ:ID:NO:5核苷酸所示。
3.根据权利要求1所述的通过基因编辑降低水稻直链淀粉含量的方法,其特征在于,所述水稻为水稻品种638S和华占。
4.一种特异sgRNA,其特征在于,其靶标序列如下:ATCCACAACATCTCCTACCA。
5.一种抑制水稻中Waxy基因的表达的方法,其特征在于,包括如下步骤:借助CRISPR/Cas9系统通过对水稻Waxy基因进行基因编辑从而抑制水稻Waxy基因的表达;所述CRISPR/Cas9系统中,sgRNA的靶标序列如下:ATCCACAACATCTCCTACCA;所述水稻具体可为水稻品种638S和华占。
CN201911186091.1A 2019-11-28 2019-11-28 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA Active CN110714010B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201911186091.1A CN110714010B (zh) 2019-11-28 2019-11-28 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201911186091.1A CN110714010B (zh) 2019-11-28 2019-11-28 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA

Publications (2)

Publication Number Publication Date
CN110714010A CN110714010A (zh) 2020-01-21
CN110714010B true CN110714010B (zh) 2022-11-04

Family

ID=69216516

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201911186091.1A Active CN110714010B (zh) 2019-11-28 2019-11-28 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA

Country Status (1)

Country Link
CN (1) CN110714010B (zh)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111424036B (zh) * 2020-03-16 2021-11-02 华中农业大学 水稻新Wx等位基因及其在育种中的应用
CN111560395B (zh) * 2020-04-09 2022-10-04 华南农业大学 一种调控作物种子直链淀粉含量和胶稠度的方法及应用
WO2021254268A1 (zh) * 2020-06-15 2021-12-23 山东舜丰生物科技有限公司 一种改变植物直链淀粉含量的多肽、核酸及其应用
CN113174379B (zh) * 2020-06-15 2021-11-26 山东舜丰生物科技有限公司 一种提高植物直链淀粉含量的多肽、核酸及其应用
CN113462702B (zh) * 2020-06-22 2023-06-27 山东舜丰生物科技有限公司 一种突变型waxy基因及其应用
CN112175905B (zh) * 2020-09-30 2022-07-22 上海中医药大学 一种高效敲除nk细胞中cd96基因的方法
CN112126661B (zh) * 2020-09-30 2022-07-22 上海中医药大学 一种高效敲除nk细胞中tigit基因的方法
CN113637688B (zh) * 2021-09-23 2023-10-13 上海师范大学 水稻稻米直链淀粉含量调控基因OsACF1及其应用
CN114058639B (zh) * 2021-10-29 2023-11-07 中国种子集团有限公司 利用单碱基基因编辑技术突变OsWaxy基因改良水稻直链淀粉含量的方法
CN114085853B (zh) * 2021-11-25 2024-05-17 湖南省核农学与航天育种研究所 Waxy突变体及其筛选方法和用途

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109207513A (zh) * 2018-10-22 2019-01-15 中国科学院遗传与发育生物学研究所 Dcm1蛋白及其编码基因在调控植物雄性育性中的应用
CN109355304A (zh) * 2018-11-15 2019-02-19 中国农业科学院作物科学研究所 一种创制玉米甜糯籽粒种质的方法
CN109705198A (zh) * 2019-01-25 2019-05-03 扬州大学 OsCKX7蛋白质及其编码基因在调控植物纹枯病抗性中的应用

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109207513A (zh) * 2018-10-22 2019-01-15 中国科学院遗传与发育生物学研究所 Dcm1蛋白及其编码基因在调控植物雄性育性中的应用
CN109355304A (zh) * 2018-11-15 2019-02-19 中国农业科学院作物科学研究所 一种创制玉米甜糯籽粒种质的方法
CN109705198A (zh) * 2019-01-25 2019-05-03 扬州大学 OsCKX7蛋白质及其编码基因在调控植物纹枯病抗性中的应用

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Targeted mutagenesis using the Agrobacterium tumefaciens-mediated CRISPR-Cas9 system in common wheat;Zhang Shujuan等;《BMC Plant Biology》;20181231;第18卷(第1期);全文 *

Also Published As

Publication number Publication date
CN110714010A (zh) 2020-01-21

Similar Documents

Publication Publication Date Title
CN110714010B (zh) 一种通过基因编辑降低水稻直链淀粉含量的方法及其专用sgRNA
JP5562295B2 (ja) 分枝酵素の活性を改変した小麦、ならびにそれから得たデンプンおよびデンプン含有品
RU2619636C2 (ru) Высокоамилозная пшеница
CN111197034B (zh) 基于基因编辑技术的Wx突变型蛋白及其基因在植物育种中的应用
CN102933072A (zh) 大麦及其用途
JP2009509509A (ja) コーヒー中のスクロース分解と関連している核酸及びタンパク質
US20080201807A1 (en) Gelatinization Temperature Manipulation
CN102250226B (zh) 一种与水稻产量相关蛋白及其编码基因与应用
Elkonin et al. Development of sorghum mutants with improved in vitro protein digestibility by CRISPR/Cas9 editing of kafirin genes
CN113862265A (zh) 一种改良水稻粒型和外观品质的方法
US11576326B2 (en) Wheat with new alleles of Rht-B1
CN104450757B (zh) 调控水稻穗型和粒型的sl基因及其应用
JP7410030B2 (ja) 高められた加水分解酵素活性を有する大麦
JP4711762B2 (ja) スターチシンターゼIIIa型の機能解明と新規デンプン作出法
CN110092819A (zh) 玉米苞叶宽度调控蛋白arf2及其编码基因与应用
CN114107322A (zh) 调控番茄果实可溶性固形物含量的基因的用途
US7619134B2 (en) Starches produced by the expression of heterologous granule bound starch synthase genes
JP3513192B2 (ja) 新規なイネ澱粉枝つけ酵素遺伝子
CN114231557B (zh) 水稻种子休眠性调控基因及其用途
CN1330719A (zh) 影响植物的开花行为的手段和方法
CN111849974B (zh) 一种水稻Wx基因的启动子Wxb7及用途
CN111849975B (zh) 一种水稻Wx基因的启动子Wxb2及用途
US20150044349A1 (en) Methods of controlling fructan synthesis in plants
US6881433B1 (en) Food products containing altered starch
CN117660495A (zh) OsMDH基因在提高稻米品质中的应用

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