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Cloning of high molecular weight gluten subunit promoter and study on its function in wheat

机译:高分子量面筋亚基启动子的克隆及其在小麦中的功能研究

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The aim of this work was to study the cloning and characterization of HMW-GS 1Dx2 promoter from Triticum aestivum. A 1050 bp partial promoter fragment including a putative TATA box and 5' encoding sequence of the gene was cloned by amplifying the upstream sequences using the nest-PCR with appropriate primers. The analysis of the promoter sequence against the PLACE (Plant cis-acting Regulatory DNA Elements) database showed the presence of certain putative endosperm-specific regulatory cis-elements in the sequence along with the TATA and CAAT boxes. The histochemical method detected the transient expressions of GUS in the seeds of wheat. The results showed that HMW-GS 1Dx2 promoter had the endosperm-specific transcription activity in the wheat seeds.
机译:这项工作的目的是研究小麦的HMW-GS 1Dx2启动子的克隆和鉴定。通过使用带有适当引物的巢式PCR扩增上游序列,克隆了一个1050 bp的部分启动子片段,其中包括一个推定的TATA盒和该基因的5'编码序列。针对PLACE(植物顺式作用调控DNA元件)数据库的启动子序列分析显示,该序列中存在某些推定的胚乳特异性调控顺式元件以及TATA和CAAT框。组织化学方法检测到GUS在小麦种子中的瞬时表达。结果表明,HMW-GS 1Dx2启动子在小麦种子中具有胚乳特异性转录活性。

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