DNA repair and recovery of RNA synthesis following exposure to ultraviolet light are delayed in long genes

被引:66
作者
Andrade-Lima, Leonardo C. [1 ,2 ,3 ]
Veloso, Artur [1 ,2 ,4 ]
Paulsen, Michelle T. [1 ,2 ]
Menck, Carlos F. M. [3 ]
Ljungman, Mats [1 ,2 ,5 ]
机构
[1] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Translat Oncol Program, Ann Arbor, MI 48109 USA
[3] Univ Sao Paulo, Inst Biomed Sci, Dept Microbiol, Sao Paulo, Brazil
[4] Univ Michigan, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Environm Hlth Sci, Ann Arbor, MI 48109 USA
基金
巴西圣保罗研究基金会;
关键词
POLYMERASE-II; TRANSCRIBED STRAND; DHFR GENE; SACCHAROMYCES-CEREVISIAE; INDUCED UBIQUITINATION; PYRIMIDINE DIMERS; INDUCED APOPTOSIS; EXCISION-REPAIR; DAMAGE; REMOVAL;
D O I
10.1093/nar/gkv148
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
The kinetics of DNA repair and RNA synthesis recovery in human cells following UV-irradiation were assessed using nascent RNA Bru-seq and quantitative long PCR. It was found that UV light inhibited transcription elongation and that recovery of RNA synthesis occurred as a wave in the 5'-3' direction with slow recovery and TC-NER at the 3' end of long genes. RNA synthesis resumed fully at the 3'-end of genes after a 24 h recovery in wild-type fibroblasts, but not in cells deficient in transcription-coupled nucleotide excision repair (TC-NER) or global genomic NER (GG-NER). Different transcription recovery profiles were found for individual genes but these differences did not fully correlate to differences in DNA repair of these genes. Our study gives the first genomewide view of how UV-induced lesions affect transcription and how the recovery of RNA synthesis of large genes are particularly delayed by the apparent lack of resumption of transcription by arrested polymerases.
引用
收藏
页码:2744 / 2756
页数:13
相关论文
共 36 条
[1]   Transcription Recovery after DNA Damage Requires Chromatin Priming by the H3.3 Histone Chaperone HIRA [J].
Adam, Salome ;
Polo, Sophie E. ;
Almouzni, Genevieve .
CELL, 2013, 155 (01) :94-106
[2]   Strand-specific PCR of UV radiation-damaged genomic DNA revealed an essential role of DNA-PKcs in the transcription-coupled repair [J].
An, Jing ;
Yang, Tianyi ;
Huang, Yuecheng ;
Liu, Feng ;
Sun, Jingfen ;
Wang, Yu ;
Xu, Qingzhi ;
Wu, Dechang ;
Zhou, Pingkun .
BMC BIOCHEMISTRY, 2011, 12
[3]  
[Anonymous], 2005, DNA REPAIR MUTAGENES
[4]   DNA-REPAIR IN AN ACTIVE GENE - REMOVAL OF PYRIMIDINE DIMERS FROM THE DHFR GENE OF CHO CELLS IS MUCH MORE EFFICIENT THAN IN THE GENOME OVERALL [J].
BOHR, VA ;
SMITH, CA ;
OKUMOTO, DS ;
HANAWALT, PC .
CELL, 1985, 40 (02) :359-369
[5]   UV-induced ubiquitination of RNA polymerase II: A novel modification deficient in cockayne syndrome cells [J].
Bregman, DB ;
Halaban, R ;
vanGool, AJ ;
Henning, KA ;
Friedberg, EC ;
Warren, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) :11586-11590
[6]   CPD damage recognition by transcribing RNA polymerase II [J].
Brueckner, Florian ;
Hennecke, Ulrich ;
Carell, Thomas ;
Cramer, Patrick .
SCIENCE, 2007, 315 (5813) :859-862
[7]  
Furda Amy M, 2012, Methods Mol Biol, V920, P111, DOI 10.1007/978-1-61779-998-3_9
[8]   Transcription-coupled DNA repair: two decades of progress and surprises [J].
Hanawalt, Philip C. ;
Spivak, Graciela .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (12) :958-970
[9]   Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources [J].
Huang, Da Wei ;
Sherman, Brad T. ;
Lempicki, Richard A. .
NATURE PROTOCOLS, 2009, 4 (01) :44-57
[10]   NER Factors Are Recruited to Active Promoters and Facilitate Chromatin Modification for Transcription in the Absence of Exogenous Genotoxic Attack [J].
Le May, Nicolas ;
Mota-Fernandes, David ;
Velez-Cruz, Renier ;
Iltis, Izarn ;
Biard, Denis ;
Egly, Jean Marc .
MOLECULAR CELL, 2010, 38 (01) :54-66