4.8 Article

RECQL5 Controls Transcript Elongation and Suppresses Genome Instability Associated with Transcription Stress

期刊

CELL
卷 157, 期 5, 页码 1037-1049

出版社

CELL PRESS
DOI: 10.1016/j.cell.2014.03.048

关键词

-

资金

  1. Association for International Cancer Research
  2. European Research Council
  3. Cancer Research UK
  4. Cancer Research UK [11567] Funding Source: researchfish
  5. Worldwide Cancer Research [09-0730] Funding Source: researchfish

向作者/读者索取更多资源

RECQL5 is the solemember of theRECQfamily of helicases associated with RNA polymerase II ( RNAPII). We now show that RECQL5 is a general elongation factor that is important for preserving genome stability during transcription. Depletion or overexpression of RECQL5 results in corresponding shifts in the genome- wide RNAPII density profile. Elongation is particularly affected, with RECQL5 depletion causing a striking increase in the average rate, concurrent with increased stalling, pausing, arrest, and/ or backtracking ( transcription stress). RECQL5 therefore controls the movement of RNAPII across genes. Loss of RECQL5 also results in the loss or gain of genomic regions, with the breakpoints of lost regions located in genes and common fragile sites. The chromosomal breakpoints overlap with areas of elevated transcription stress, suggesting thatRECQL5 suppresses such stress and its detrimental effects, and thereby prevents genome instability in the transcribed region of genes.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据