苜蓿MsLEA3-1 ihpRNA表达载体的构建及其在烟草中的遗传转化

Q3 Agricultural and Biological Sciences Acta Agronomica Sinica Pub Date : 2010-09-01 DOI:10.1016/S1875-2780(09)60073-0
Yong-Qin BAI , Jun-Mei KANG , Yan SUN , Qing-Chuan YANG , Yan LI
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引用次数: 1

摘要

晚期胚胎发生丰富蛋白(LEA)是植物胁迫生理学研究的热点之一。本研究构建了含紫花苜蓿MsLEA3-1基因片段的RNAi表达载体。根据MsLEA3-1 (GenBank登录号EU665182)序列设计两对不同酶位点的特异性引物。构建PMD-LEA质粒模板,获得正义链和反义链,分别插入表达载体pART27中。通过酶切证实了RNAi载体pART-F-R的发夹结构。通过农杆菌介导的转化体系将pART-F-R转化为烟草,经PCR验证获得16株转基因植株。
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Construction of ihpRNA Expression Vector of MsLEA3-1 from Medicago sativa L. and Genetic Transformation in Tobacco

Late embriogenesis abundant (LEA) protein is one of the hot topics in plant stress physiology. In this study, an RNAi expression vector harboring MsLEA3-1 gene fragment from alfalfa (Medicago sativa L.) was constructed. Two pairs of specific primers with different enzyme sites were designed based on the sequence of MsLEA3-1 (GenBank accession number EU665182). With the template of PMD-LEA plasmid constructed, positive-sense strand and antisense strand were obtained, which were separately inserted into the expression vector pART27. A hairpin structure in the RNAi vector pART-F-R was confirmed by the digestion of restriction enzymes. pART-F-R was transformed into tobacco via Agrobacterium-mediated transformation system, and 16 transgenic plants were obtained after PCR validation.

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30 weeks
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