Consequences and Resolution of Transcription-Replication Conflicts

被引:20
|
作者
Lalonde, Maxime [1 ]
Trauner, Manuel [1 ]
Werner, Marcel [1 ]
Hamperl, Stephan [1 ]
机构
[1] Helmholtz Zentrum Munchen, Inst Epigenet & Stem Cells IES, D-81377 Munich, Germany
来源
LIFE-BASEL | 2021年 / 11卷 / 07期
基金
欧洲研究理事会;
关键词
transcription-replication conflicts; genomic instability; R-loops; torsional stress; common fragile sites; early replicating fragile sites; replication stress; chromatin; fork reversal; MIDAS; G-MiDS; COMMON FRAGILE SITES; POLYMERASE-II TRANSCRIPTION; R-LOOP FORMATION; DNA-REPLICATION; FACILITATES REPLICATION; RIBOSOMAL-RNA; S-PHASE; GENOMIC INSTABILITY; FORK PROGRESSION; MESSENGER-RNA;
D O I
10.3390/life11070637
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcription-replication conflicts occur when the two critical cellular machineries responsible for gene expression and genome duplication collide with each other on the same genomic location. Although both prokaryotic and eukaryotic cells have evolved multiple mechanisms to coordinate these processes on individual chromosomes, it is now clear that conflicts can arise due to aberrant transcription regulation and premature proliferation, leading to DNA replication stress and genomic instability. As both are considered hallmarks of aging and human diseases such as cancer, understanding the cellular consequences of conflicts is of paramount importance. In this article, we summarize our current knowledge on where and when collisions occur and how these encounters affect the genome and chromatin landscape of cells. Finally, we conclude with the different cellular pathways and multiple mechanisms that cells have put in place at conflict sites to ensure the resolution of conflicts and accurate genome duplication.
引用
收藏
页数:25
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