Yong-Qin BAI , Jun-Mei KANG , Yan SUN , Qing-Chuan YANG , Yan LI
{"title":"Construction of ihpRNA Expression Vector of MsLEA3-1 from Medicago sativa L. and Genetic Transformation in Tobacco","authors":"Yong-Qin BAI , Jun-Mei KANG , Yan SUN , Qing-Chuan YANG , Yan LI","doi":"10.1016/S1875-2780(09)60073-0","DOIUrl":null,"url":null,"abstract":"<div><p>Late embriogenesis abundant (LEA) protein is one of the hot topics in plant stress physiology. In this study, an RNAi expression vector harboring <em>MsLEA3-1</em> gene fragment from alfalfa (<em>Medicago sativa</em> L.) was constructed. Two pairs of specific primers with different enzyme sites were designed based on the sequence of <em>MsLEA3-1</em> (GenBank accession number <span>EU665182</span><svg><path></path></svg>). 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 <em>Agrobacterium</em>-mediated transformation system, and 16 transgenic plants were obtained after PCR validation.</p></div>","PeriodicalId":7085,"journal":{"name":"Acta Agronomica Sinica","volume":"36 9","pages":"Pages 1484-1489"},"PeriodicalIF":0.0000,"publicationDate":"2010-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1875-2780(09)60073-0","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Agronomica Sinica","FirstCategoryId":"1091","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1875278009600730","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 1
Abstract
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.