Suppr超能文献

酿酒酵母DNA聚合酶δ基因中温度敏感突变的抑制子

Suppressors of thermosensitive mutations in the DNA polymerase delta gene of Saccharomyces cerevisiae.

作者信息

Giot L, Simon M, Dubois C, Faye G

机构信息

Institut Curie-Biologie, Centre Universitaire, Orsay, France.

出版信息

Mol Gen Genet. 1995 Jan 20;246(2):212-22. doi: 10.1007/BF00294684.

Abstract

DNA polymerases (Pol) alpha, delta and epsilon are necessary for replication of nuclear DNA. Pol delta interacts permanently or transiently with numerous accessory proteins whose identification may shed light on the function(s) of Pol delta. In vitro mutagenesis was used to induce thermosensitive (ts) mutations in the DNA polymerase delta gene (POL3). We have attempted to clone two recessive extragenic suppressors of such ts mutants (sdp1 for mutation pol3-14 and sdp5-1 for mutation pol3-11) by transforming thermoresistant haploid strains pol3-14 sdp1 and pol3-11 sdp5-1 with wild-type genomic libraries in singlecopy or multicopy vectors. None of the thermosensitive transformants so obtained was identified as being sdp1 or sdp5-1. Instead, three genes were cloned whose products interfere with the activity of suppressors. One of them is the type 1 protein phosphatase gene, DIS2. Another is a novel gene, ASM4, whose gene product is rich in asparagine and glutamine residues.

摘要

DNA聚合酶(Pol)α、δ和ε是核DNA复制所必需的。Pol δ与众多辅助蛋白永久或短暂相互作用,对这些辅助蛋白的鉴定可能有助于揭示Pol δ的功能。体外诱变用于在DNA聚合酶δ基因(POL3)中诱导温度敏感(ts)突变。我们试图通过用单拷贝或多拷贝载体中的野生型基因组文库转化耐热单倍体菌株pol3-14 sdp1和pol3-11 sdp5-1,来克隆此类ts突变体的两个隐性基因外抑制子(pol3-14突变的sdp1和pol3-11突变的sdp5-1)。如此获得的温度敏感转化体均未被鉴定为sdp1或sdp5-1。相反,克隆了三个基因,其产物会干扰抑制子的活性。其中一个是1型蛋白磷酸酶基因DIS2。另一个是新基因ASM4,其基因产物富含天冬酰胺和谷氨酰胺残基。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验