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酵母逆转录转座子Ty2-917的GCR1依赖性转录激活

GCR1-dependent transcriptional activation of yeast retrotransposon Ty2-917.

作者信息

Türkel S, Liao X B, Farabaugh P J

机构信息

Department of Biology, Faculty of Arts & Sciences, Abant izzet Baysal University, Bolu, Turkey.

出版信息

Yeast. 1997 Aug;13(10):917-30. doi: 10.1002/(SICI)1097-0061(199708)13:10<917::AID-YEA148>3.0.CO;2-G.

Abstract

Transcription of Saccharomyces cerevisiae Ty2-917 retrotransposon depends on regulatory elements both upstream and downstream of the transcription initiation site. An upstream activation sequence (UAS) and a downstream enhancer stimulate transcription synergistically. Here we show that activation by both of these sites depends on the GCR1 product, a transcription factor which also regulates the genes encoding yeast glycolytic enzymes. Eliminating GCR1 causes a 100-fold decrease in transcription of Ty2-917. Activation by the isolated Ty2-917 UAS also strongly depends on GCR1. Unexpectedly, GCR1-dependent activation by the Ty2-917 enhancer is strongly position-dependent. Activation by the enhancer in its normal position within the transcription unit depended strongly on GCR1, but eliminating GCR1 reduced activation only three-fold when the enhancer was moved upstream of the transcribed region. Gel mobility shift and DNaseI protection assays indicated that GCR1 binds specifically to multiple sites within the Ty2-917 UAS and enhancer regions.

摘要

酿酒酵母Ty2-917逆转座子的转录依赖于转录起始位点上游和下游的调控元件。一个上游激活序列(UAS)和一个下游增强子协同刺激转录。在这里,我们表明这两个位点的激活都依赖于GCR1产物,一种转录因子,它也调节编码酵母糖酵解酶的基因。消除GCR1会导致Ty2-917转录下降100倍。分离的Ty2-917 UAS的激活也强烈依赖于GCR1。出乎意料的是,Ty2-917增强子的GCR1依赖性激活强烈依赖于位置。增强子在转录单元内正常位置的激活强烈依赖于GCR1,但当增强子移至转录区域上游时,消除GCR1仅使激活降低三倍。凝胶迁移率变动分析和DNaseI保护分析表明,GCR1特异性结合Ty2-917 UAS和增强子区域内的多个位点。

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