Chromatin remodeling by Pol II primes efficient Pol III transcription

被引:6
|
作者
Yague-Sanz, Carlo [1 ]
Migeot, Valerie [1 ]
Larochelle, Marc [2 ]
Bachand, Francois [2 ]
Wery, Maxime [3 ]
Morillon, Antonin [3 ]
Hermand, Damien [1 ]
机构
[1] Univ Namur, URPHYM GEMO, Rue Bruxelles 61, B-5000 Namur, Belgium
[2] Univ Sherbrooke, Dept Biochem & Funct Genom, RNA Grp, Sherbrooke, PQ J1E 4K8, Canada
[3] Univ Paris 06, PSL Res Univ, CNRS UMR 3244, NcRNA,Epigenet & Genome Fluid,Inst Curie, Paris, France
关键词
RNA-POLYMERASE-III; HISTONE H3; TERMINAL DOMAIN; EXPRESSION; MAF1; RECRUITMENT; REVEALS; SUBUNIT; GENES; RSC;
D O I
10.1038/s41467-023-39387-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcription of RNA polymerase II is coupled with remodeling of chromatin. This study reports that transcription of RNA polymerase II is also required to prime and maintain nucleosome depletion at RNA polymerase III loci. The packaging of the genetic material into chromatin imposes the remodeling of this barrier to allow efficient transcription. RNA polymerase II activity is coupled with several histone modification complexes that enforce remodeling. How RNA polymerase III (Pol III) counteracts the inhibitory effect of chromatin is unknown. We report here a mechanism where RNA Polymerase II (Pol II) transcription is required to prime and maintain nucleosome depletion at Pol III loci and contributes to efficient Pol III recruitment upon re-initiation of growth from stationary phase in Fission yeast. The Pcr1 transcription factor participates in the recruitment of Pol II, which affects local histone occupancy through the associated SAGA complex and a Pol II phospho-S2 CTD / Mst2 pathway. These data expand the central role of Pol II in gene expression beyond mRNA synthesis.
引用
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页数:13
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