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酿酒酵母中粟酒裂殖酵母ADH基因转录起始所需的DNA序列元件。

DNA sequence elements required for transcription initiation of the Schizosaccharomyces pombe ADH gene in Saccharomyces cerevisiae.

作者信息

Furter-Graves E M, Hall B D

机构信息

Department of Genetics SK-50, University of Washington, Seattle 98195.

出版信息

Mol Gen Genet. 1990 Sep;223(3):407-16. doi: 10.1007/BF00264447.

Abstract

The roles of the TATA element and sequences near the mRNA initiation site in specifying the location of initiation sites in Saccharomyces cerevisiae were examined, using the Schizosaccharomyces pombe ADH gene. The importance of spacing was demonstrated by analysis of a series of deletions that removed from 8-50 bp between the TATA element and ATG translation initiation site of this gene. Primer extension mapping showed that increasing deletion length is associated with a progressive shift downstream in the location of the initiation sites. The distance of a given site from the promoter affected the relative ability of the site to be utilized for initiation. For this gene, a permissive region for transcription initiation exists between 55 and 125 bases downstream of the TATA element, and a zone of 75-115 bases allows maximal usage of an initiation site. The presence of a TATA sequence was shown to be necessary in S. cerevisiae for maintaining the location of this "window" of initiation. The TATA sequence is essential for function of the gene in S. pombe. This gene, as well as the majority of the 63 S. cerevisiae genes surveyed, uses initiation sites which fit a PyAA/T(Pu) consensus. Cis-acting mutations were recovered which restored ADH activity to a deletion allele that initiates its mRNAs downstream of the ATG. DNA sequence and transcript analysis with these mutants confirmed the requirement of proper spacing and conformity of initiation sites to the PyAA/T(Pu) consensus for efficient transcript initiation.

摘要

利用粟酒裂殖酵母ADH基因,研究了酿酒酵母中TATA元件和mRNA起始位点附近序列在确定起始位点位置方面的作用。通过分析一系列缺失突变,这些突变从该基因的TATA元件与ATG翻译起始位点之间去除了8 - 50个碱基对,证明了间隔的重要性。引物延伸图谱显示,缺失长度增加与起始位点位置逐渐向下游移动有关。给定位点与启动子的距离影响该位点用于起始的相对能力。对于该基因,转录起始的允许区域存在于TATA元件下游55至125个碱基之间,75 - 115个碱基的区域允许起始位点的最大利用。在酿酒酵母中,TATA序列的存在被证明对于维持这个起始“窗口”的位置是必要的。TATA序列对于粟酒裂殖酵母中该基因的功能至关重要。该基因以及所检测的63个酿酒酵母基因中的大多数,使用符合PyAA/T(Pu)共有序列的起始位点。分离到了顺式作用突变,这些突变恢复了一个缺失等位基因的ADH活性,该缺失等位基因在ATG下游起始其mRNA。对这些突变体的DNA序列和转录本分析证实了适当间隔以及起始位点符合PyAA/T(Pu)共有序列对于有效转录起始的必要性。

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