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粟酒裂殖酵母rec16基因产物调控多个减数分裂事件。

The Schizosaccharomyces pombe rec16 gene product regulates multiple meiotic events.

作者信息

Li Y F, Smith G R

机构信息

Fred Hutchinson Cancer Research Center, Seattle, Washington 98104, USA.

出版信息

Genetics. 1997 May;146(1):57-67. doi: 10.1093/genetics/146.1.57.

Abstract

Previously isolated meiotic recombination (rec) mutants of Schizosaccharomyces pombe define 16 complementation groups. The rec genes cloned and sequenced to date reveal little amino acid sequence identity to other reported proteins. We examined the rec mutants for alterations in meiotic events other than recombination to gain insight into the rec gene functions and to assess whether they affect recombination directly or indirectly. While mutations in the rec6-12, 14, 15 and 19 genes appeared to affect only meiotic recombination, a mutation in rec16 delayed meiotic DNA synthesis and, in some instances, reduced its amount; mitotic DNA synthesis was not detectably altered, indicating that the rec16 effect is limited to meiosis. In the rec16 mutant some meiotically induced transcripts (e.g., rec7 and 15) were significantly reduced in abundance, whereas others (e.g., rec10 and exo1) were induced and degraded with normal timing and extent during meiosis, indicating that the rec16 mutation leaves the basic meiotic program intact. These results indicate that the rec genes other than rec16 have their primary effect on meiotic recombination. In contrast, the rec16 gene product is essential for normal meiotic replication, recombination, and induction of some transcripts. These meiotic events may be coupled via a dependence of recombination and transcription on replication or via a cascade of gene expression.

摘要

先前分离得到的粟酒裂殖酵母减数分裂重组(rec)突变体可分为16个互补群。迄今为止克隆并测序的rec基因与其他已报道的蛋白质几乎没有氨基酸序列同源性。我们研究了rec突变体在除重组之外的减数分裂事件中的变化,以深入了解rec基因的功能,并评估它们是直接还是间接影响重组。虽然rec6 - 12、14、15和19基因的突变似乎仅影响减数分裂重组,但rec16基因的突变延迟了减数分裂DNA合成,并且在某些情况下减少了其合成量;有丝分裂DNA合成未检测到明显变化,这表明rec16的作用仅限于减数分裂。在rec16突变体中,一些减数分裂诱导的转录本(如rec7和15)的丰度显著降低,而其他转录本(如rec10和exo1)在减数分裂期间正常时间和程度地被诱导和降解,这表明rec16突变并未破坏基本的减数分裂程序。这些结果表明,除rec16外的rec基因主要影响减数分裂重组。相比之下,rec16基因产物对于正常的减数分裂复制、重组以及一些转录本的诱导是必需的。这些减数分裂事件可能通过重组和转录对复制的依赖性或通过基因表达的级联反应而相互关联。

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