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酿酒酵母nin1-1的多拷贝抑制因子是黑腹果蝇双酚氧化酶A2基因Dox-A2的对应物。

A multicopy suppressor of nin1-1 of the yeast Saccharomyces cerevisiae is a counterpart of the Drosophila melanogaster diphenol oxidase A2 gene, Dox-A2.

作者信息

Kawamura M, Kominami K, Takeuchi J, Toh-e A

机构信息

Department of Biological Sciences, Graduate School of Science, University of Tokyo, Japan.

出版信息

Mol Gen Genet. 1996 May 23;251(2):146-52. doi: 10.1007/BF02172912.

Abstract

NIN1 is an essential gene for growth of the yeast Saccharomyces cerevisiae and was recently found to encode a component of the regulatory subunit of the 26S proteasome. The nin1-1 mutant is temperature sensitive and its main defect is in G1/S progression and G2/M progression at non-permissive temperatures. One of the two multicopy suppressors of nin1-1, SUN2 (SUppressor of Nin1-1), was found to encode a protein of 523 amino acids whose sequence is similar to those of Drosophila melanogaster diphenol oxidase A2 and the mouse mast-cell Tum(-) transplantation antigen, P91A. The C-terminal half of Sun2p was found to be functional as Sun2p at 25 degrees C, 30 degrees C, and 34 degrees C but not at 37 degrees C. The open reading frame (ORF) of the Drosophila diphenol oxidase A2 gene (Dox-A2) was obtained from a lambda phage cDNA library using the polymerase chain reaction technique. The Dox-A2 ORF driven by the TDH3 promoter complemented the phenotype of a strain deleted for sun2. This Dox-A2-dependent strain was temperature sensitive and accumulated dumb-bell-shaped cells, with an undivided nucleus at the isthmus, after temperature upshift. This morphology is similar to that of nin1-1 cells kept at a restrictive temperature. These results suggest that SUN2 is a functional counterpart of Dox-A2 and that these genes play a pivotal role in the cell cycle in each organism.

摘要

NIN1是酿酒酵母生长所必需的基因,最近发现它编码26S蛋白酶体调节亚基的一个组成部分。nin1-1突变体对温度敏感,其主要缺陷在于在非允许温度下的G1/S期进展和G2/M期进展。nin1-1的两个多拷贝抑制子之一SUN2(Nin1-1的抑制子)被发现编码一种由523个氨基酸组成的蛋白质,其序列与黑腹果蝇双酚氧化酶A2和小鼠肥大细胞Tum(-)移植抗原P91A的序列相似。发现Sun2p的C端一半在25℃、30℃和34℃时具有Sun2p的功能,但在37℃时则没有。使用聚合酶链反应技术从λ噬菌体cDNA文库中获得了果蝇双酚氧化酶A2基因(Dox-A2)的开放阅读框(ORF)。由TDH3启动子驱动的Dox-A2 ORF补充了缺失sun2的菌株的表型。这种依赖Dox-A2的菌株对温度敏感,在温度升高后积累哑铃形细胞,在峡部有一个未分裂的细胞核。这种形态与在限制温度下培养的nin1-1细胞的形态相似。这些结果表明SUN2是Dox-A2的功能对应物,并且这些基因在每个生物体的细胞周期中都起着关键作用。

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