TRIM28 regulates RNA polymerase II promoter-proximal pausing and pause release

被引:108
作者
Bunch, Heeyoun [1 ]
Zheng, Xiaofeng [2 ]
Burkholder, Adam [3 ]
Dillon, Simon T. [1 ,4 ]
Motola, Shmulik [5 ]
Birrane, Gabriel [1 ,6 ]
Ebmeier, Christopher C. [7 ]
Levine, Stuart [5 ]
Fargo, David [3 ]
Hu, Guang [2 ]
Taatjes, Dylan J. [7 ]
Calderwood, Stuart K. [1 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Radiat Oncol, Boston, MA 02215 USA
[2] NIEHS, Mol Carcinogenesis Lab, NIH, Res Triangle Pk, NC 27709 USA
[3] NIEHS, NIH, Res Triangle Pk, NC 27709 USA
[4] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Genom & Prote Ctr, Boston, MA 02215 USA
[5] MIT, BioMicro Ctr, Cambridge, MA 02139 USA
[6] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Med, Boston, MA 02215 USA
[7] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
POL-II; DROSOPHILA-EMBRYO; IN-VIVO; TRANSCRIPTION; GENOME; GENES; EXPRESSION; REVEALS; NELF; ATM;
D O I
10.1038/nsmb.2878
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
Promoter-proximal pausing of RNA polymerase II (Pol II) is a major checkpoint in transcription. An unbiased search for new human proteins that could regulate paused Pol II at the HSPA1B gene identified TRIM28. In vitro analyses indicated HSF1-dependent attenuation of Pol II pausing upon TRIM28 depletion, whereas in vivo data revealed de novo expression of HSPA1B and other known genes regulated by paused Pol II upon TRIM28 knockdown. These results were supported by genome-wide ChIP-sequencing analyses of Pol II occupancy that revealed a global role for TRIM28 in regulating Pol II pausing and pause release. Furthermore, in vivo and in vitro mechanistic studies suggest that transcription-coupled phosphorylation regulates Pol II pause release by TRIM28. Collectively, our findings identify TRIM28 as a new factor that modulates Pol II pausing and transcriptional elongation at a large number of mammalian genes.
引用
收藏
页码:876 / 883
页数:8
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