Transcription and chromatin-based surveillance mechanism controls suppression of cryptic antisense transcription
Author(s) -
Donghyuk Heo,
Krzysztof Kuś,
Pawel Grzechnik,
Sue Mei TanWong,
Adrien Birot,
Tea Kecman,
Søren Nielsen,
Nikolay Zenkin,
Lidia Vasiljeva
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.109671
Subject(s) - rna polymerase ii , biology , transcription (linguistics) , chromatin , antisense rna , microbiology and biotechnology , transcription factor ii d , transcription preinitiation complex , eukaryotic transcription , general transcription factor , rna polymerase ii holoenzyme , transcription factor ii b , genetics , rna , gene expression , gene , rna polymerase , promoter , linguistics , philosophy
Summary Phosphorylation of the RNA polymerase II C-terminal domain Y 1 S 2 P 3 T 4 S 5 P 6 S 7 consensus sequence coordinates key events during transcription, and its deregulation leads to defects in transcription and RNA processing. Here, we report that the histone deacetylase activity of the fission yeast Hos2/Set3 complex plays an important role in suppressing cryptic initiation of antisense transcription when RNA polymerase II phosphorylation is dysregulated due to the loss of Ssu72 phosphatase. Interestingly, although single Hos2 and Set3 mutants have little effect, loss of Hos2 or Set3 combined with ssu72 Δ results in a synergistic increase in antisense transcription globally and correlates with elevated sensitivity to genotoxic agents. We demonstrate a key role for the Ssu72/Hos2/Set3 mechanism in the suppression of cryptic antisense transcription at the 3′ end of convergent genes that are most susceptible to these defects, ensuring the fidelity of gene expression within dense genomes of simple eukaryotes.
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