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酿酒酵母1号染色体DNA的分子克隆:MAK16基因的分离及对低温生长必需的一个相邻基因的分析

Molecular cloning of chromosome I DNA from Saccharomyces cerevisiae: isolation of the MAK16 gene and analysis of an adjacent gene essential for growth at low temperatures.

作者信息

Wickner R B, Koh T J, Crowley J C, O'Neil J, Kaback D B

机构信息

Section on Genetics of Simple Eukaryotes, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.

出版信息

Yeast. 1987 Mar;3(1):51-7. doi: 10.1002/yea.320030108.

Abstract

MAK16 is an essential gene on chromosome I defined by the thermosensitive lethal mak16-1 mutation. MAK16 is also necessary for M double-stranded RNA replication at the permissive temperature for cell growth. As part of an effort to clone all the DNA from chromosome I, plasmids that complemented both the temperature-sensitive growth defect, and the M1 replication defects of mak16-1 strains were isolated from a plasmid YCp50: Saccharomyces cerevisiae recombinant DNA library. The two plasmids analysed contained overlapping inserts that hybridized proportionally to strains carrying different dosages of chromosome I. Furthermore, integration of a fragment of one of these clones occurred at a site linked to ade 1, confirming that this clone was derived from the appropriate region of chromosome I. An open reading frame adjacent to MAK16 potentially coding for a 468 amino acid protein was defined by sequence analysis. 185 amino acids of this open reading frame were replaced with a 1.2 kb fragment carrying the S. cerevisiae URA3 gene by a one-step gene disruption. The resulting strains grew at a rate indistinguishable from the wild type at 20 degrees C, 30 degrees C, or 37 degrees C, but could not grow at 8 degrees C. The deleted region is thus essential only at 8 degrees C, and we name this gene LTE1 (low temperature essential).

摘要

MAK16是位于第一条染色体上的一个必需基因,由温度敏感致死突变体mak16-1所定义。在细胞生长的允许温度下,MAK16对于M双链RNA的复制也是必需的。作为从第一条染色体克隆所有DNA的工作的一部分,从质粒YCp50:酿酒酵母重组DNA文库中分离出了能够互补mak16-1菌株的温度敏感生长缺陷和M1复制缺陷的质粒。所分析的两个质粒含有重叠的插入片段,这些片段与携带不同剂量第一条染色体的菌株成比例地杂交。此外,其中一个克隆的片段整合发生在与ade 1连锁的位点,证实该克隆源自第一条染色体的适当区域。通过序列分析确定了一个与MAK16相邻的开放阅读框,其可能编码一个468个氨基酸的蛋白质。通过一步基因破坏,将该开放阅读框的185个氨基酸替换为携带酿酒酵母URA3基因的1.2 kb片段。所得菌株在20℃、30℃或37℃下的生长速率与野生型无明显差异,但在8℃下不能生长。因此,缺失区域仅在8℃时是必需的,我们将这个基因命名为LTE1(低温必需基因)。

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