Suppr超能文献

酿酒酵母DNA链转移蛋白β基因DST2的克隆与特性分析

Cloning and characterization of DST2, the gene for DNA strand transfer protein beta from Saccharomyces cerevisiae.

作者信息

Dykstra C C, Kitada K, Clark A B, Hamatake R K, Sugino A

机构信息

Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.

出版信息

Mol Cell Biol. 1991 May;11(5):2583-92. doi: 10.1128/mcb.11.5.2583-2592.1991.

Abstract

The gene encoding the 180-kDa DNA strand transfer protein beta from the yeast Saccharomyces cerevisiae was identified and sequenced. This gene, DST2 (DNA strand transferase 2), was located on chromosome VII. dst2 gene disruption mutants exhibited temperature-sensitive sporulation and a 50% longer generation time during vegetative growth than did the wild type. Spontaneous mitotic recombination in the mutants was reduced severalfold for both intrachromosomal recombination and intragenic gene conversion. The mutants also had reduced levels of the intragenic recombination that is induced during meiosis. Meiotic recombinants were, however, somewhat unstable in the mutants, with a decrease in recombinants and survival upon prolonged incubation in sporulation media. spo13 or spo13 rad50 mutations did not relieve the sporulation defect of dst2 mutations. A dst1 dst2 double mutant has the same phenotype as a dst2 single mutant. All phenotypes associated with the dst2 mutations could be complemented by a plasmid containing DST2.

摘要

编码来自酿酒酵母的180-kDa DNA链转移蛋白β的基因被鉴定并测序。该基因,即DST2(DNA链转移酶2),位于第七条染色体上。dst2基因破坏突变体表现出温度敏感的孢子形成,并且在营养生长期间的代时比野生型长50%。对于染色体内重组和基因内基因转换,突变体中的自发有丝分裂重组减少了几倍。突变体中减数分裂期间诱导的基因内重组水平也降低。然而,减数分裂重组体在突变体中有些不稳定,在孢子形成培养基中长时间孵育后重组体减少且存活率降低。spo13或spo13 rad50突变不能缓解dst2突变的孢子形成缺陷。dst1 dst2双突变体与dst2单突变体具有相同的表型。与dst2突变相关的所有表型都可以被含有DST2的质粒互补。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b6c/360028/77e8c3a775a3/molcellb00139-0264-a.jpg

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