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酿酒酵母MET3基因:核苷酸序列以及5'非编码区与MET25基因5'非编码区的关系。

The Saccharomyces cerevisiae MET3 gene: nucleotide sequence and relationship of the 5' non-coding region to that of MET25.

作者信息

Cherest H, Kerjan P, Surdin-Kerjan Y

机构信息

Laboratoire d'Enzymologie du C.N.R.S., Gif-sur-Yvette, France.

出版信息

Mol Gen Genet. 1987 Dec;210(2):307-13. doi: 10.1007/BF00325699.

Abstract

In Saccharomyces cerevisiae, the expression of several genes implicated in methionine biosynthesis is co-regulated by a specific negative control. To elucidate the molecular basis of this regulation, we have cloned two of these genes, MET3 and MET25. The sequence of MET25 has already been determined (Kerjan et al. 1986). Here, we report the nucleotide sequence of the MET3 gene along with its 5' and 3' flanking regions. Plasmids bearing different deletions upstream of the transcribed region of MET3 were constructed. They were introduced into yeast cells and tested for their ability to complement met3 mutations and to respond to regulation by exogenous methionine. The regulatory region was located within a 100 bp region. The sequence of this regulatory region was compared with that of MET25. A short common sequence which occurs 250-280 bp upstream of the translation initiation codon of the gene was found. This sequence is a good candidate for the cis-acting regulatory element.

摘要

在酿酒酵母中,几个与甲硫氨酸生物合成相关的基因的表达受一种特定的负调控共同调节。为了阐明这种调控的分子基础,我们克隆了其中两个基因,MET3和MET25。MET25的序列已经确定(Kerjan等人,1986年)。在此,我们报告MET3基因的核苷酸序列及其5'和3'侧翼区域。构建了携带MET3转录区上游不同缺失的质粒。将它们导入酵母细胞,并测试其互补met3突变以及对外源甲硫氨酸调控作出反应的能力。调控区域位于一个100 bp的区域内。将该调控区域的序列与MET25的序列进行了比较。发现在该基因翻译起始密码子上游250 - 280 bp处有一个短的共有序列。这个序列是顺式作用调控元件的一个很好的候选者。

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