Yong-Qin BAI , Jun-Mei KANG , Yan SUN , Qing-Chuan YANG , Yan LI
{"title":"苜蓿MsLEA3-1 ihpRNA表达载体的构建及其在烟草中的遗传转化","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":"{\"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}","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}
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.