Double stranded DNA breaks and genome editing trigger loss of ribosomal protein RPS27A

被引:17
作者
Riepe, Celeste [1 ]
Zelin, Elena [2 ]
Frankino, Phillip A. [1 ]
Meacham, Zuriah A. [1 ]
Fernandez, Samantha G. [1 ]
Ingolia, Nicholas T. [1 ]
Corn, Jacob E. [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, 16 Barker Hall 3202, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Innovat Genom Inst, Berkeley, CA 94720 USA
[3] ETH, Dept Biol, HPL J 36,Otto Stern Weg 7, CH-8093 Zurich, Switzerland
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
DNA damage response; genome editing; ribosomes; translation; TRANSLATION INITIATION; SPECIALIZED RIBOSOMES; MESSENGER-RNAS; ACTIVATION; RECRUITMENT; CANCER;
D O I
10.1111/febs.16321
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
DNA damage activates a robust transcriptional stress response, but much less is known about how DNA damage impacts translation. The advent of genome editing with Cas9 has intensified interest in understanding cellular responses to DNA damage. Here, we find that DNA double-strand breaks (DSBs), including those induced by Cas9, trigger the loss of ribosomal protein RPS27A from ribosomes via p53-independent proteasomal degradation. Comparisons of Cas9 and dCas9 ribosome profiling and mRNA-seq experiments reveal a global translational response to DSBs that precedes changes in transcript abundance. Our results demonstrate that even a single DSB can lead to altered translational output and ribosome remodeling, suggesting caution in interpreting cellular phenotypes measured immediately after genome editing.
引用
收藏
页码:3101 / 3114
页数:14
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