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首页> 外文期刊>National Academy Science Letters >PCR amplification, cloning and In-silico characterization of promoter regions of HMW-glutenin, alpha/beta-gliadin and triticin genes from wheat variety K-68
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PCR amplification, cloning and In-silico characterization of promoter regions of HMW-glutenin, alpha/beta-gliadin and triticin genes from wheat variety K-68

机译:小麦品种K-68的HMW-谷蛋白,α/β-gliadin和triticin基因的启动子区域的PCR扩增,克隆和计算机芯片鉴定

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摘要

HMW-glutenin and alpha/beta-gliadin promoter regions were amplified through PCR from wheat variety K-68 using primers designed on the basis of published nucleotide sequences of HMW-glutenin and alpha/beta-gliadin genes of wheat variety Chinese Spring.In addition, an 821 bp promoter'region of triticin gene was also amplified and cloned from K-68, using genome walking strategy. Nucleotide sequences of the cloned promoter regions were analyzed using promoter analysis softwares like PLACE and Promoter Scan which revealed the presence of several cw-acting regulatory motifs required for driving endosperm specific expression of the genes. Several promoter elements, having diverse functions, were also identified in the cloned promoter regions.
机译:使用基于中国春小麦HMW-谷蛋白和α/β-麦醇溶蛋白基因的公开核苷酸序列设计的引物,通过PCR扩增小麦K-68的HMW-谷蛋白和α/β-麦醇溶蛋白启动子区域。利用基因组步移策略,也从K-68中扩增并克隆了一个triticin基因的821 bp启动子区域。使用诸如PLACE和Promoter Scan的启动子分析软件分析了克隆的启动子区域的核苷酸序列,该软件揭示了驱动基因胚乳特异性表达所需的几个顺式作用调节基序的存在。在克隆的启动子区域中还鉴定了几种具有多种功能的启动子元件。

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