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Sub1在渗透调节以及RNA聚合酶II和III的转录过程中发挥作用。

Sub1 functions in osmoregulation and in transcription by both RNA polymerases II and III.

作者信息

Rosonina Emanuel, Willis Ian M, Manley James L

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Mol Cell Biol. 2009 Apr;29(8):2308-21. doi: 10.1128/MCB.01841-08. Epub 2009 Feb 9.

Abstract

Sub1 is implicated in transcriptional activation, elongation, and mRNA 3'-end formation in budding yeast. To gain more insight into its function, we performed a synthetic genetic array screen with SUB1 that uncovered genetic interactions with genes involved in the high-osmolarity glycerol (HOG) osmoresponse pathway. We find that Sub1 and the HOG pathway are redundant for survival in moderate osmolarity. Chromatin immunoprecipitation analysis shows that Sub1 is recruited to osmoresponse gene promoters during osmotic shock and is required for full recruitment of TBP, TFIIB, and RNA polymerase II (RNAP II) at a subset of these genes. Furthermore, we detect Sub1 at the promoter of every constitutively transcribed RNAP II and, unexpectedly, at every RNAP III gene tested, but not at the RNAP I-transcribed ribosomal DNA promoter. Significantly, deletion of SUB1 reduced levels of promoter-associated RNAP II or III at these genes, but not TBP levels. Together these data suggest that, in addition to a general role in polymerase recruitment at constitutive RNAP II and RNAP III genes, during osmotic shock, Sub1 facilitates osmoresponse gene transcription by enhancing preinitiation complex formation.

摘要

Sub1在芽殖酵母的转录激活、延伸和mRNA 3'端形成过程中发挥作用。为了更深入了解其功能,我们对SUB1进行了合成遗传阵列筛选,发现它与参与高渗甘油(HOG)渗透压反应途径的基因存在遗传相互作用。我们发现,在中等渗透压条件下,Sub1和HOG途径对于细胞存活是冗余的。染色质免疫沉淀分析表明,在渗透应激期间,Sub1被招募到渗透压反应基因的启动子上,并且在这些基因的一个子集中,它是TBP、TFIIB和RNA聚合酶II(RNAP II)完全招募所必需的。此外,我们在每个组成型转录的RNAP II的启动子处检测到Sub1,出乎意料的是,在每个测试的RNAP III基因处也检测到了Sub1,但在RNAP I转录的核糖体DNA启动子处未检测到。值得注意的是,SUB1的缺失降低了这些基因处与启动子相关的RNAP II或III的水平,但不影响TBP的水平。这些数据共同表明,除了在组成型RNAP II和RNAP III基因的聚合酶招募中发挥一般作用外,在渗透应激期间,Sub1通过增强起始前复合物的形成来促进渗透压反应基因的转录。

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