R Loops Are Linked to Histone H3 S10 Phosphorylation and Chromatin Condensation

被引:210
作者
Castellano-Pozo, Maikel [1 ]
Santos-Pereira, Jose M. [1 ]
Rondon, Ana G. [1 ]
Barroso, Sonia [1 ]
Andujar, Eloisa [2 ]
Perez-Alegre, Monica [2 ]
Garcia-Muse, Tatiana [1 ]
Aguilera, Andres [1 ,2 ]
机构
[1] Univ Sevilla CS1C, Dept Mol Biol, Seville 41092, Spain
[2] Univ Sevilla CS1C, Ctr Andaluz Biol Mol & Med Regenerat CABIMER, Genom Unit, Seville 41092, Spain
关键词
REPLICATION FORK PROGRESSION; GENOME INSTABILITY; SACCHAROMYCES-CEREVISIAE; RNA/DNA HYBRIDS; TRANSCRIPTION; RNA; YEAST; PHOSPHATASE; IMPAIRMENT; STABILITY;
D O I
10.1016/j.molcel.2013.10.006
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
R loops are transcription byproducts that constitute a threat to genome integrity. Here we show that R loops are tightly linked to histone H3 S10 phosphorylation (H3S10P), a mark of chromatin condensation. Chromatin immunoprecipitation (ChIP)-on-chip (ChIP-chip) analyses reveal H3S10P accumulation at centromeres, pericentromeric chromatin, and a large number of active open reading frames (ORFs) in R-loop-accumulating yeast cells, better observed in G1. Histone H3S10 plays a key role in maintaining genome stability, as scored by ectopic recombination and plasmid loss, Rad52 foci, and Rad53 checkpoint activation. H3S10P coincides with the presence of DNA-RNA hybrids, is suppressed by ribonuclease H overexpression, and causes reduced accessibility of restriction endonucleases, implying a tight connection between R loops, H3S10P, and chromatin compaction. Such histone modifications were also observed in R-loop-accumulating Caenorhabditis elegans and He La cells. We therefore provide a role of RNA in chromatin structure essential to understand how R loops modulate genome dynamics.
引用
收藏
页码:583 / 590
页数:8
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