Physiological functions of programmed DNA breaks in signal-induced transcription

被引:48
作者
Puc, Janusz [1 ,2 ]
Aggarwal, Aneel K. [3 ]
Rosenfeld, Michael G. [2 ]
机构
[1] EMD Serono Res & Dev Inst, Billerica, MA 01821 USA
[2] Univ Calif San Diego, Sch Med, Howard Hughes Med Inst, Dept Med, La Jolla, CA 92093 USA
[3] Icahn Sch Med Mt Sinai, Dept Pharmacol Sci, New York, NY 10029 USA
关键词
DOUBLE-STRAND BREAKS; RNA-POLYMERASE-II; DEPENDENT PROTEIN-KINASE; ESTROGEN-RECEPTOR-ALPHA; NEURAL STEM/PROGENITOR CELLS; TOPOISOMERASE-I; PROSTATE-CANCER; POLY(ADP-RIBOSE) POLYMERASE; ANDROGEN RECEPTOR; SUPER-ENHANCERS;
D O I
10.1038/nrm.2017.43
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The idea that signal-dependent transcription might involve the generation of transient DNA nicks or even breaks in the regulatory regions of genes, accompanied by activation of DNA damage repair pathways, would seem to be counterintuitive, as DNA damage is usually considered harmful to cellular integrity. However, recent studies have generated a substantial body of evidence that now argues that programmed DNA single-or double-strand breaks can, at least in specific cases, have a role in transcription regulation. Here, we discuss the emerging functions of DNA breaks in the relief of DNA torsional stress and in promoter and enhancer activation.
引用
收藏
页码:471 / 476
页数:6
相关论文
共 77 条
[1]   Temporal activation of XRCC1-mediated DNA repair is essential for muscle differentiation [J].
Al-Khalaf, Mohammad H. ;
Blake, Leanne E. ;
Larsen, Brian D. ;
Bell, Ryan A. ;
Brunette, Steve ;
Parks, Robin J. ;
Rudnicki, Michael A. ;
McKinnon, Peter J. ;
Dilworth, F. Jeffrey ;
Megeney, Lynn A. .
CELL DISCOVERY, 2016, 2
[2]   Topoisomerase-mediated chromosomal break repair: an emerging player in many games [J].
Ashour, Mohamed E. ;
Atteya, Reham ;
El-Khamisy, Sherif F. .
NATURE REVIEWS CANCER, 2015, 15 (03) :137-151
[3]   The transcriptional regulator Aire binds to and activates super-enhancers [J].
Bansal, Kushagra ;
Yoshida, Hideyuki ;
Benoist, Christophe ;
Mathis, Diane .
NATURE IMMUNOLOGY, 2017, 18 (03) :263-273
[4]   RNA Polymerase II Regulates Topoisomerase 1 Activity to Favor Efficient Transcription [J].
Baranello, Laura ;
Wojtowicz, Damian ;
Cui, Kairong ;
Devaiah, Ballachanda N. ;
Chung, Hye-Jung ;
Chan-Salis, Ka Yim ;
Guha, Rajarshi ;
Wilson, Kelli ;
Zhang, Xiaohu ;
Zhang, Hongliang ;
Piotrowski, Jason ;
Thomas, Craig J. ;
Singer, Dinah S. ;
Pugh, B. Franklin ;
Pommier, Yves ;
Przytycka, Teresa M. ;
Kouzine, Fedor ;
Lewis, Brian A. ;
Zhao, Keji ;
Levens, David .
CELL, 2016, 165 (02) :357-371
[5]   Transcription blockage by homopurine DNA sequences: role of sequence composition and single-strand breaks [J].
Belotserkovskii, Boris P. ;
Neil, Alexander J. ;
Saleh, Syed Shayon ;
Shin, Jane Hae Soo ;
Mirkin, Sergei M. ;
Hanawalt, Philip C. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (03) :1817-1828
[6]   NKX3.1 homeodomain protein binds to topoisomerase I and enhances its activity [J].
Bowen, Cai ;
Stuart, August ;
Ju, Jeong-Ho ;
Tuan, Jenny ;
Blonder, Josip ;
Conrads, Thomas P. ;
Veenstra, Timothy D. ;
Gelmann, Edward P. .
CANCER RESEARCH, 2007, 67 (02) :455-464
[7]   NKX3.1 Activates Cellular Response to DNA Damage [J].
Bowen, Cai ;
Gelmann, Edward P. .
CANCER RESEARCH, 2010, 70 (08) :3089-3097
[8]   Transcriptional elongation requires DNA break-induced signalling [J].
Bunch, Heeyoun ;
Lawney, Brian P. ;
Lin, Yu-Fen ;
Asaithamby, Aroumougame ;
Murshid, Ayesha ;
Wang, Yaoyu E. ;
Chen, Benjamin P. C. ;
Calderwood, Stuart K. .
NATURE COMMUNICATIONS, 2015, 6
[9]   DNA topoisomerases: Structure, function, and mechanism [J].
Champoux, JJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :369-413
[10]   Deletion of Individual Ku Subunits in Mice Causes an NHEJ-Independent Phenotype Potentially by Altering Apurinic/Apyrimidinic Site Repair [J].
Choi, Yong Jun ;
Li, Han ;
Son, Mi Young ;
Wang, Xiao-hong ;
Fornsaglio, Jamie L. ;
Sobol, Robert W. ;
Lee, Moonsook ;
Vijg, Jan ;
Imholz, Sandra ;
Dolle, Martijn E. T. ;
van Steeg, Harry ;
Reiling, Erwin ;
Hasty, Paul .
PLOS ONE, 2014, 9 (01)