Suppr超能文献

DNA损伤和热休克双重调控酿酒酵母中的基因。

DNA damage and heat shock dually regulate genes in Saccharomyces cerevisiae.

作者信息

McClanahan T, McEntee K

出版信息

Mol Cell Biol. 1986 Jan;6(1):90-6. doi: 10.1128/mcb.6.1.90-96.1986.

Abstract

Two Saccharomyces cerevisiae genes isolated in a differential hybridization screening for DNA damage regulation (DDR genes) were also transcriptionally regulated by heat shock treatment. A 0.45-kilobase transcript homologous to the DDRA2 gene and a 1.25-kilobase transcript homologous to the DDR48 gene accumulated after exposure of cells to 4-nitroquinoline-1-oxide (NQO; 1 to 1.5 microgram/ml) or brief heat shock (20 min at 37 degrees C). The DDRA2 transcript, which was undetectable in untreated cells, was induced to high levels by these treatments, and the DDR48 transcript increased more than 10-fold as demonstrated by Northern hybridization analysis. Two findings argue that dual regulation of stress-responsive genes is not common in S. cerevisiae. First, two members of the heat shock-inducible hsp70 family of S. cerevisiae, YG100 and YG102, were not induced by exposure to NQO. Second, at least one other DNA-damage-inducible gene, DIN1, was not regulated by heat shock treatment. We examined the structure of the induced RNA homologous to DDRA2 after heat shock and NQO treatments by S1 nuclease protection experiments. Our results demonstrated that the DDRA2 transcript initiates equally frequently at two sites separated by 5 base pairs. Both transcriptional start sites were utilized when cells were exposed to either NQO or heat shock treatment. These results indicate that DDRA2 and DDR48 are members of a unique dually regulated stress-responsive family of genes in S. cerevisiae.

摘要

在针对DNA损伤调控的差异杂交筛选中分离出的两个酿酒酵母基因(DDR基因),也受到热休克处理的转录调控。与DDRA2基因同源的0.45千碱基转录本和与DDR48基因同源的1.25千碱基转录本,在细胞暴露于4-硝基喹啉-1-氧化物(NQO;1至1.5微克/毫升)或短暂热休克(37℃处理20分钟)后积累。在未处理的细胞中无法检测到的DDRA2转录本,经这些处理后被诱导至高水平,并且通过Northern杂交分析表明DDR48转录本增加了10倍以上。有两个发现表明应激反应基因的双重调控在酿酒酵母中并不常见。第一,酿酒酵母热休克诱导型hsp70家族的两个成员YG100和YG102,在暴露于NQO后未被诱导。第二,至少一个其他的DNA损伤诱导基因DIN1,不受热休克处理的调控。我们通过S1核酸酶保护实验检查了热休克和NQO处理后与DDRA2同源的诱导RNA的结构。我们的结果表明,DDRA2转录本在相隔5个碱基对的两个位点起始频率相同。当细胞暴露于NQO或热休克处理时,两个转录起始位点均被利用。这些结果表明,DDRA2和DDR48是酿酒酵母中一个独特的双重调控应激反应基因家族的成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c39/367487/175a6bce24ea/molcellb00085-0112-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验