HAN Zhao-Xue , QIAN Gang , PAN Zhi-Fen , DENG Guang-Bing , WU Fang , TANG Ya-Wei , QIANG Xiao-Lin , YU Mao-Qun
{"title":"西藏无壳大麦(Hordeum vulgare subsp) 4个b -苦苷基因的克隆与特性分析。)","authors":"HAN Zhao-Xue , QIAN Gang , PAN Zhi-Fen , DENG Guang-Bing , WU Fang , TANG Ya-Wei , QIANG Xiao-Lin , YU Mao-Qun","doi":"10.1016/S0379-4172(06)60128-5","DOIUrl":null,"url":null,"abstract":"<div><p>Four B-hordein genes, designated <em>BH1-BH4</em>, were cloned using PCR amplification from two hull-less barley cultivars, ZQ7239 and ZQ148, collected from Tibet. The results of sequencing indicated that <em>BH1-BH4</em> contained complete open reading frames (ORFs). Comparison of their predicted polypeptide sequences with the published sequences suggested that they all share the same basic protein structure. Phylogenetic analysis indicated that the deduced amino-acid sequences of <em>BH1-BH4</em> genes were more closely related to B-hordeins from cultivated barley (<em>Hordeum vulgare</em> L.) than to any other prolamins from wild barley and <em>Aegilops tauschii</em>. Comparison of the coding regions of <em>BH1-BH4</em> genes showed that <em>BH1</em> had a lower sequence identity to other previously published B-hordeins than the other three B-hordeins obtained in this study. <em>BH1</em> was then cloned in a bacterial expression vector based on bacteriophage T7 RNA polymerase. The resulting plasmid produced a 28.15 kDa protein in <em>Escherichia coli</em>. The potential value of B-hordein genes in grain quality improvement of hull-less barley has been discussed.</p></div>","PeriodicalId":100017,"journal":{"name":"Acta Genetica Sinica","volume":"33 10","pages":"Pages 937-947"},"PeriodicalIF":0.0000,"publicationDate":"2006-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60128-5","citationCount":"3","resultStr":"{\"title\":\"Cloning and Characterization of Four B-hordein Genes from Tibetan Hull-less Barley (Hordeum vulgare subsp. vulgare)\",\"authors\":\"HAN Zhao-Xue , QIAN Gang , PAN Zhi-Fen , DENG Guang-Bing , WU Fang , TANG Ya-Wei , QIANG Xiao-Lin , YU Mao-Qun\",\"doi\":\"10.1016/S0379-4172(06)60128-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Four B-hordein genes, designated <em>BH1-BH4</em>, were cloned using PCR amplification from two hull-less barley cultivars, ZQ7239 and ZQ148, collected from Tibet. The results of sequencing indicated that <em>BH1-BH4</em> contained complete open reading frames (ORFs). Comparison of their predicted polypeptide sequences with the published sequences suggested that they all share the same basic protein structure. Phylogenetic analysis indicated that the deduced amino-acid sequences of <em>BH1-BH4</em> genes were more closely related to B-hordeins from cultivated barley (<em>Hordeum vulgare</em> L.) than to any other prolamins from wild barley and <em>Aegilops tauschii</em>. Comparison of the coding regions of <em>BH1-BH4</em> genes showed that <em>BH1</em> had a lower sequence identity to other previously published B-hordeins than the other three B-hordeins obtained in this study. <em>BH1</em> was then cloned in a bacterial expression vector based on bacteriophage T7 RNA polymerase. The resulting plasmid produced a 28.15 kDa protein in <em>Escherichia coli</em>. The potential value of B-hordein genes in grain quality improvement of hull-less barley has been discussed.</p></div>\",\"PeriodicalId\":100017,\"journal\":{\"name\":\"Acta Genetica Sinica\",\"volume\":\"33 10\",\"pages\":\"Pages 937-947\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60128-5\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Genetica Sinica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0379417206601285\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Genetica Sinica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0379417206601285","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cloning and Characterization of Four B-hordein Genes from Tibetan Hull-less Barley (Hordeum vulgare subsp. vulgare)
Four B-hordein genes, designated BH1-BH4, were cloned using PCR amplification from two hull-less barley cultivars, ZQ7239 and ZQ148, collected from Tibet. The results of sequencing indicated that BH1-BH4 contained complete open reading frames (ORFs). Comparison of their predicted polypeptide sequences with the published sequences suggested that they all share the same basic protein structure. Phylogenetic analysis indicated that the deduced amino-acid sequences of BH1-BH4 genes were more closely related to B-hordeins from cultivated barley (Hordeum vulgare L.) than to any other prolamins from wild barley and Aegilops tauschii. Comparison of the coding regions of BH1-BH4 genes showed that BH1 had a lower sequence identity to other previously published B-hordeins than the other three B-hordeins obtained in this study. BH1 was then cloned in a bacterial expression vector based on bacteriophage T7 RNA polymerase. The resulting plasmid produced a 28.15 kDa protein in Escherichia coli. The potential value of B-hordein genes in grain quality improvement of hull-less barley has been discussed.