Transcriptional elongation requires DNA break-induced signalling

被引:154
作者
Bunch, Heeyoun [1 ]
Lawney, Brian P. [2 ]
Lin, Yu-Fen [3 ]
Asaithamby, Aroumougame [3 ]
Murshid, Ayesha [1 ]
Wang, Yaoyu E. [2 ]
Chen, Benjamin P. C. [3 ]
Calderwood, Stuart K. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Radiat Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Ctr Canc Computat Biol, Boston, MA 02130 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, Dallas, TX 75390 USA
关键词
DEPENDENT PROTEIN-KINASE; DOUBLE-STRAND BREAKS; TOPOISOMERASE-II; RNA-POLYMERASE; POL II; H2AX PHOSPHORYLATION; EXPRESSION; PROMOTER; GAMMA-H2AX; CHROMATIN;
D O I
10.1038/ncomms10191
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have previously shown that RNA polymerase II (Pol II) pause release and transcriptional elongation involve phosphorylation of the factor TRIM28 by the DNA damage response (DDR) kinases ATM and DNA-PK. Here we report a significant role for DNA breaks and DDR signalling in the mechanisms of transcriptional elongation in stimulus-inducible genes in humans. Our data show the enrichment of TRIM28 and gamma H2AX on serum-induced genes and the important function of DNA-PK for Pol II pause release and transcriptional activation-coupled DDR signalling on these genes. gamma H2AX accumulation decreases when P-TEFb is inhibited, confirming that DDR signalling results from transcriptional elongation. In addition, transcriptional elongation-coupled DDR signalling involves topoisomerase II because inhibiting this enzyme interferes with Pol II pause release and gamma H2AX accumulation. Our findings propose that DDR signalling is required for effective Pol II pause release and transcriptional elongation through a novel mechanism involving TRIM28, DNA-PK and topoisomerase II.
引用
收藏
页数:12
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