|本期目录/Table of Contents|

[1]王雷,崔震海,张立军.玉米C4型PEPC全长基因的克隆与表达载体构建[J].江苏农业科学,2014,42(11):26-29.
 Wang Lei,et al().Cloning and expression vector construction of full-length C4 type PEPC gene in maize[J].Jiangsu Agricultural Sciences,2014,42(11):26-29.
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玉米C4PEPC全长基因的克隆与表达载体构建(PDF)
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《江苏农业科学》[ISSN:1002-1302/CN:32-1214/S]

卷:
第42卷
期数:
2014年11期
页码:
26-29
栏目:
生物技术
出版日期:
2014-11-25

文章信息/Info

Title:
Cloning and expression vector construction of full-length C4 type PEPC gene in maize
作者:
王雷 崔震海 张立军
沈阳农业大学生物科学技术学院/辽宁省植物基因工程技术研究中心,辽宁沈阳 110866
Author(s):
Wang Leiet al(26)
关键词:
玉米PEPC基因克隆序列分析表达载体构建
Keywords:
-
分类号:
Q786;S513.01
DOI:
-
文献标志码:
A
摘要:
以玉米自交系郑58基因组DNA为模板,设计了2对特异性引物,分别PCR扩增玉米C4型磷酸烯醇式丙酮酸羧化酶(PEPC)启动子及其全长编码序列,利用In-Fusion技术将两者定向克隆到载体pCAMBIA-1391Z上,并对重组子进行测序验证。结果表明,该PEPC启动子序列与GenBank中的玉米自交系B73的同源性为97.70%,片段长1 200 bp;全长编码序列同源性为97.90%,片段长6 330 bp。通过Hind Ⅲ和EcoRⅠ酶切载体pCAMBIA-1391Z,利用In-Fusion技术将线性载体与之前获得的2个PCR片段连接,测序结果与预期序列一致,表明成功构建了 pCAMBIA-1391Z-PEPC 植物表达载体。对克隆和载体构建中存在的问题进行了讨论,以期为该类型基因的高效克隆及表达载体的构建提供参考、为C4 PEPC基因功能研究和C3植物遗传转化提供可用的基因序列。
Abstract:
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参考文献/References:

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备注/Memo

备注/Memo:
收稿日期:2014-01-12
基金项目:国家自然科学基金(编号:31000673);教育部博士点基金(编号:20102103110001、20102103120001);辽宁省科技厅科技攻关项目(编号:201201238)。
作者简介:王雷(1987—),男,山东菏泽人,硕士研究生,研究方向为植物基因工程与分子生物学。E-mail:wanglei6399@126.com。
通信作者:张立军,博士,教授,主要从事植物发育与作物生物技术研究。Tel:(024) 88187613;E-mail:lijunzhang8@yahoo.com.cn。
更新日期/Last Update: 2014-11-25