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粟酒裂殖酵母中区域特异性减数分裂重组:rec11基因

Region-specific meiotic recombination in Schizosaccharomyces pombe: the rec11 gene.

作者信息

Li Y F, Numata M, Wahls W P, Smith G R

机构信息

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

出版信息

Mol Microbiol. 1997 Mar;23(5):869-78. doi: 10.1046/j.1365-2958.1997.2691632.x.

Abstract

Mutations in the rec11 gene of Schizosaccharomyces pombe reduce meiotic recombinant frequencies by as much as a factor of 300 on chromosome III but less than a factor of 4 in the intervals tested on chromosomes I and II. To gain insight into the function of this region- (or chromosome-) specific activator of recombination, we have cloned and sequenced the rec11 gene. Meiotic crosses with rec11 disruption mutations placed the rec11 gene 6 cM from ade6 on chromosome III. Transcripts of rec11 accumulated transiently at 2-3 h after induction of melosis in a pat1-114 (Ts) mutant. Reverse transcriptase/polymerase chain reaction (RT-PCR) analysis of these transcripts revealed eight introns. The spliced RNA is predicted to encode a polypeptide of 923 amino acids with only very limited homology to reported proteins. The transient accumulation of rec11 transcripts and the phenotype of rec11 mutations suggest that the novel rec11 gene product acts early in meiosis to activate recombination preferentially on chromosome III.

摘要

粟酒裂殖酵母rec11基因的突变使III号染色体上的减数分裂重组频率降低多达300倍,但在I号和II号染色体上测试的区间内,重组频率降低不到4倍。为深入了解这个区域(或染色体)特异性重组激活因子的功能,我们克隆并测序了rec11基因。用rec11破坏突变进行的减数分裂杂交将rec11基因定位在III号染色体上距ade6基因6厘摩处。在pat1-114(Ts)突变体中,rec11的转录本在减数分裂诱导后2 - 3小时短暂积累。对这些转录本进行逆转录酶/聚合酶链反应(RT-PCR)分析发现了8个内含子。预测剪接后的RNA编码一个923个氨基酸的多肽,与已报道的蛋白质只有非常有限的同源性。rec11转录本的短暂积累以及rec11突变的表型表明,新的rec11基因产物在减数分裂早期起作用,优先激活III号染色体上的重组。

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