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Acetylation-Dependent Recruitment of the FACT Complex and Its Role in Regulating Pol II Occupancy Genome-Wide in Saccharomyces cerevisiae .

Authors :
Pathak R
Singh P
Ananthakrishnan S
Adamczyk S
Schimmel O
Govind CK
Source :
Genetics [Genetics] 2018 Jul; Vol. 209 (3), pp. 743-756. Date of Electronic Publication: 2018 Apr 25.
Publication Year :
2018

Abstract

Histone chaperones, chromatin remodelers, and histone modifying complexes play a critical role in alleviating the nucleosomal barrier for DNA-dependent processes. Here, we have examined the role of two highly conserved yeast ( Saccharomyces cerevisiae ) histone chaperones, facilitates chromatin transcription (FACT) and Spt6, in regulating transcription. We show that the H3 tail contributes to the recruitment of FACT to coding sequences in a manner dependent on acetylation. We found that deleting a H3 histone acetyltransferase Gcn5 or mutating lysines on the H3 tail impairs FACT recruitment at ADH1 and ARG1 genes. However, deleting the H4 tail or mutating the H4 lysines failed to dampen FACT occupancy in coding regions. Additionally, we show that FACT depletion reduces RNA polymerase II (Pol II) occupancy genome-wide. Spt6 depletion leads to a reduction in Pol II occupancy toward the 3'-end, in a manner dependent on the gene length. Severe transcription and histone-eviction defects were also observed in a strain that was impaired for Spt6 recruitment ( spt6 Δ202) and depleted of FACT. Importantly, the severity of the defect strongly correlated with wild-type Pol II occupancies at these genes, indicating critical roles for Spt6 and Spt16 in promoting high-level transcription. Collectively, our results show that both FACT and Spt6 are important for transcription globally and may participate during different stages of transcription.<br /> (Copyright © 2018 by the Genetics Society of America.)

Details

Language :
English
ISSN :
1943-2631
Volume :
209
Issue :
3
Database :
MEDLINE
Journal :
Genetics
Publication Type :
Academic Journal
Accession number :
29695490
Full Text :
https://doi.org/10.1534/genetics.118.300943