High-Throughput Genetic and Gene Expression Analysis of the RNAPII-CTD Reveals Unexpected Connections to SRB10/CDK8

被引:19
作者
Aristizabal, Maria J. [1 ]
Negri, Gian Luca [2 ]
Benschop, Joris J. [3 ]
Holstege, Frank C. P. [3 ]
Krogan, Nevan J. [4 ]
Kobor, Michael S. [1 ]
机构
[1] Univ British Columbia, Dept Med Genet, Child & Family Res Inst, Ctr Mol Med & Therapeut, Vancouver, BC, Canada
[2] Univ Coll Dublin, Sch Med & Med Sci, Dublin 2, Ireland
[3] Univ Med Ctr Utrecht, Utrecht, Netherlands
[4] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
基金
加拿大自然科学与工程研究理事会; 爱尔兰科学基金会;
关键词
POLYMERASE-II CTD; CARBOXY-TERMINAL DOMAIN; SACCHAROMYCES-CEREVISIAE; LARGEST SUBUNIT; TRANSCRIPTION FACTORS; REPEAT DOMAIN; MEDIATOR; YEAST; PHOSPHATASE; PROTEIN;
D O I
10.1371/journal.pgen.1003758
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The C-terminal domain (CTD) of RNA polymerase II (RNAPII) is composed of heptapeptide repeats, which play a key regulatory role in gene expression. Using genetic interaction, chromatin immunoprecipitation followed by microarrays (ChIP-on-chip) and mRNA expression analysis, we found that truncating the CTD resulted in distinct changes to cellular function. Truncating the CTD altered RNAPII occupancy, leading to not only decreases, but also increases in mRNA levels. The latter were largely mediated by promoter elements and in part were linked to the transcription factor Rpn4. The mediator subunit Cdk8 was enriched at promoters of these genes, and its removal not only restored normal mRNA and RNAPII occupancy levels, but also reduced the abnormally high cellular amounts of Rpn4. This suggested a positive role of Cdk8 in relationship to RNAPII, which contrasted with the observed negative role at the activated INO1 gene. Here, loss of CDK8 suppressed the reduced mRNA expression and RNAPII occupancy levels of CTD truncation mutants.
引用
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页数:16
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