[1]周晓婴,付三雄,陈松,等.甘蓝型油菜CRABS CLAW基因克隆及其RNA干扰载体的构建[J].江苏农业学报,2015,(04):737-742.[doi:10.3969/j.issn.1000-4440.2015.04.005]
 ZHOU Xiao-ying,FU San-xiong,CHEN Song,et al.Cloning of CRABS CLAW gene from Brassica napus and construction of its RNA interference vector[J].,2015,(04):737-742.[doi:10.3969/j.issn.1000-4440.2015.04.005]
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甘蓝型油菜CRABS CLAW基因克隆及其RNA干扰载体的构建()
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江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2015年04期
页码:
737-742
栏目:
遗传育种·生理生化
出版日期:
2015-08-31

文章信息/Info

Title:
Cloning of CRABS CLAW gene from Brassica napus and construction of its RNA interference vector
作者:
周晓婴123付三雄123陈松123张超3戚存扣123
(1.国家油菜改良中心南京分中心,江苏南京210014;2.农业部长江下游棉花与油菜重点实验室,江苏南京210014;3.江苏省农业科学院经济作物研究所,江苏南京210014)
Author(s):
ZHOU Xiao-ying123FU San-xiong123CHEN Song123ZHANG Chao3QI Cun-kou123
(1.Nanjing Sub-center of National Center of Rapeseed Crop Improvement /Key Laboratory of Cotton and Rapeseed, Nanjing 210014, China;2.Ministry of Agriculture /Institute of Industrial Crops, Nanjing 210014, China;3. Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China)
关键词:
油菜CRABS CLAW基因RNA干扰载体 
Keywords:
Brassica napus L.CRABS CLAW geneRNA interference vector
分类号:
S565.4
DOI:
10.3969/j.issn.1000-4440.2015.04.005
文献标志码:
A
摘要:
CRABS CLAW(CRC)转录因子是YABBY基因家族成员,在植物花器官发育过程中起重要作用。为进一步研究CRC转录因子在调控油菜花器官发育过程中的作用,本研究以甘蓝型油菜品种宁油10号花蕾RNA为材料,通过反转录PCR克隆到1个580 bp长度的CRC基因,并利用pHurricane中间载体构建CRC基因的反向重复序列表达框,将CRC基因片段以正向的方式连接在1个可剪切的内含子的5′末端,以反向的方式连接到该内含子的3′末端;然后将CaMV35S启动子序列和CRC基因的反向重复表达框再克隆到植物双元载体pCAMBIAI1390的pUC18多克隆位点,构建了干扰表达载体pA6-CRCi,经过酶切鉴定和测序分析,所构建的载体正确。
Abstract:
CRABS CLAW (CRC) is a member of the YABBYA transcription factor gene family and plays an important role in the development of plant flower organ. In order to study the CRC transcription factor’s function in regulating the rape flower organ development, a 580-bp segment was cloned by RT-PCR from the total RNA of rapeseed flower organ. An inverted repeated expression cassette was firstly constructed by cloning the 580-bp segment of CRC gene into an intermediate pHurrican vector. The fragment was then ligated to a spliceable fad2 intron sequence. Finally, both the inverted repeat cassette and CaMV35S promoter were inserted into the multiple clone site of binary vector pCAMBIA1390. The ihpRNA expression vector was named pA6-CRCi, and the construction of which was further confirmed by the digestion of restriction enzymes and sequencing.

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备注/Memo

备注/Memo:
收稿日期:2015-02-02 基金项目:江苏省农业科技自主创新基金项目[CX(11)4011];江苏省自然科学基金项目(BK2011668);国家“948”项目(2011-G23) 作者简介:周晓婴(1983-),女,福建宁德人,硕士,助理研究员,主要从事油菜遗传育种研究。(Tel)025-84390364;(E-mail)beibeinv@hotmail.com 通讯作者:陈松, (Tel)025-84390370;(E-mail)chensong1963@126.com
更新日期/Last Update: 2015-08-31