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一种编码EF-1αS(延伸因子1α的体细胞形式)的非洲爪蟾基因:胚胎转录所需调控元件的序列、结构及鉴定。

A Xenopus laevis gene encoding EF-1 alpha S, the somatic form of elongation factor 1 alpha: sequence, structure, and identification of regulatory elements required for embryonic transcription.

作者信息

Johnson A D, Krieg P A

机构信息

Department of Zoology, University of Texas at Austin 78712, USA.

出版信息

Dev Genet. 1995;17(3):280-90. doi: 10.1002/dvg.1020170313.

Abstract

Transcription of the Xenopus laevis EF-1 alpha S gene commences at the mid-blastula stage of embryonic development and then continues constitutively in all somatic tissues. The EF-1 alpha S promoter is extremely active in the early Xenopus embryo where EF-1 alpha S transcripts account for as much as 40% of all new polyadenylated transcripts. We have isolated the Xenopus EF-1 alpha S gene and used microinjection techniques to identify promoter elements responsible for embryonic transcription. These in vivo expression studies have identified an enhancer fragment, located approximately 4.4 kb upstream of the transcription start site, that is required for maximum expression from the EF-1 alpha S promoter. The enhancer fragment contains both an octamer and a G/C box sequence, but mutation studies indicate that the octamer plays no significant role in regulation of EF-1 alpha S expression in the embryo. The presence of a G/C element in the enhancer and of multiple G/C boxes in the proximal promoter region suggests that the G/C box binding protein, Sp1, plays a major role in the developmental regulation of EF-1 alpha S promoter activity.

摘要

非洲爪蟾EF-1α S基因的转录在胚胎发育的囊胚中期开始,然后在所有体细胞组织中持续进行。EF-1α S启动子在早期非洲爪蟾胚胎中极其活跃,其中EF-1α S转录本占所有新的多聚腺苷酸化转录本的40%之多。我们分离出了非洲爪蟾EF-1α S基因,并使用显微注射技术来鉴定负责胚胎转录的启动子元件。这些体内表达研究确定了一个增强子片段,位于转录起始位点上游约4.4 kb处,它是EF-1α S启动子实现最大表达所必需的。该增强子片段同时包含一个八聚体和一个G/C盒序列,但突变研究表明,八聚体在胚胎中EF-1α S表达的调控中不起重要作用。增强子中存在一个G/C元件以及近端启动子区域中存在多个G/C盒,这表明G/C盒结合蛋白Sp1在EF-1α S启动子活性的发育调控中起主要作用。

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