Genome-wide function of THO/TREX in active genes prevents R-loop-dependent replication obstacles

被引:174
作者
Gomez-Gonzalez, Belen [1 ]
Garcia-Rubio, Maria [1 ,2 ]
Bermejo, Rodrigo [3 ,4 ]
Gaillard, Helene [1 ,2 ]
Shirahige, Katsuhiko [5 ]
Marin, Antonio [2 ]
Foiani, Marco [3 ,4 ]
Aguilera, Andres [1 ,2 ]
机构
[1] Univ Seville, CSIC, CABIMER, Seville 41092, Spain
[2] Univ Seville, Dept Genet, Seville, Spain
[3] Fdn Ist FIRC Oncol Mol, Milan, Italy
[4] Univ Milan, Milan, Italy
[5] Univ Tokyo, Res Ctr Epigenet Dis, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo, Japan
关键词
replication impairment; R-loops; Rrm3; THO/TREX; transcription; MESSENGER-RNA EXPORT; TRANSCRIPTION-ASSOCIATED RECOMBINATION; RICH DNA-SEQUENCES; SACCHAROMYCES-CEREVISIAE; FORK PROGRESSION; THO COMPLEX; MOLECULAR EVIDENCE; II TRANSCRIPTION; BUDDING YEAST; IN-VIVO;
D O I
10.1038/emboj.2011.206
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
THO/TREX is a conserved nuclear complex that functions in mRNP biogenesis and prevents transcription-associated recombination. Whether or not it has a ubiquitous role in the genome is unknown. Chromatin immunoprecipitation (ChIP)-chip studies reveal that the Hpr1 component of THO and the Sub2 RNA-dependent ATPase have genome-wide distributions at active ORFs in yeast. In contrast to RNA polymerase II, evenly distributed from promoter to termination regions, THO and Sub2 are absent at promoters and distributed in a gradual 5' -> 3' gradient. This is accompanied by a genome-wide impact of THO-Sub2 deletions on expression of highly expressed, long and high G + C-content genes. Importantly, ChIP-chips reveal an over-recruitment of Rrm3 in active genes in THO mutants that is reduced by RNaseH1 overexpression. Our work establishes a genome-wide function for THO-Sub2 in transcription elongation and mRNP biogenesis that function to prevent the accumulation of transcription-mediated replication obstacles, including R-loops. The EMBO Journal (2011) 30, 3106-3119. doi:10.1038/emboj.2011.206; Published online 24 June 2011
引用
收藏
页码:3106 / 3119
页数:14
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