Suppr超能文献

酵母spp81/ded1突变的一个抑制子编码一种非常相似的假定的ATP依赖性RNA解旋酶。

A suppressor of yeast spp81/ded1 mutations encodes a very similar putative ATP-dependent RNA helicase.

作者信息

Jamieson D J, Beggs J D

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, UK.

出版信息

Mol Microbiol. 1991 Apr;5(4):805-12. doi: 10.1111/j.1365-2958.1991.tb00753.x.

Abstract

The spp81/ded1 mutations were isolated as suppressors of a Saccharomyces cerevisiae pre-mRNA splicing mutation, prp8-1. The SPP81/DED1 gene encodes a putative ATP-dependent RNA helicase. While attempting to clone the wild-type SPP81/DED1 gene we isolated plasmids which were able to suppress the cold-sensitive growth defect of spp81 mutants. These plasmids encoded a gene (named DBP1) which mapped to chromosome XVI and not to the SPP81/DED1 locus on chromosome XV. The cloned gene suppressed the defect of spp81/ded1 mutants when present on both high and low copy-number plasmids but complemented spp81/ded1 null mutants only when present on high copy-number plasmids. In contrast to the SPP81/DED1 gene the DBP1 gene was not essential for cell viability. The nucleotide sequence of the DBP1 gene revealed that it also encoded a putative ATP-dependent RNA helicase which showed considerable similarity at the amino acid level to the SPP81/DED1 protein.

摘要

spp81/ded1突变体是作为酿酒酵母前体mRNA剪接突变体prp8-1的抑制子而分离得到的。SPP81/DED1基因编码一种假定的ATP依赖性RNA解旋酶。在试图克隆野生型SPP81/DED1基因时,我们分离出了能够抑制spp81突变体冷敏感生长缺陷的质粒。这些质粒编码一个基因(命名为DBP1),该基因定位于第十六号染色体,而非第十五号染色体上的SPP81/DED1基因座。当克隆基因存在于高拷贝数和低拷贝数质粒上时,均可抑制spp81/ded1突变体的缺陷,但只有当存在于高拷贝数质粒上时,才能互补spp81/ded1缺失突变体。与SPP81/DED1基因不同,DBP1基因对细胞活力并非必需。DBP1基因的核苷酸序列显示,它也编码一种假定的ATP依赖性RNA解旋酶,该酶在氨基酸水平上与SPP81/DED1蛋白具有相当大的相似性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验