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Modulation of mRNA and lncRNA expression dynamics by the Set2-Rpd3S pathway

Title
Modulation of mRNA and lncRNA expression dynamics by the Set2-Rpd3S pathway
Author(s)
Kim, Ji HyunLee, Bo BaeOh, Young MiZhu, ChenchenSteinmetz, Lars M.Lee, YookyeongKim, Wan KyuLee, Sung BaeBuratowski, StephenKim, TaeSoo
Issued Date
2016-11
Citation
Nature Communications, v.7
Type
Article
Keywords
ChromatinDEACETYLATIONHISTONE MODIFICATIONSLONG NONCODING RNASMETHYLTRANSFERASEPOLYMERASE-IISACCHAROMYCES-CEREVISIAESET2 METHYLATIONTRANSCRIPTIONAL ELONGATIONYEAST
ISSN
2041-1723
Abstract
H3K36 methylation by Set2 targets Rpd3S histone deacetylase to transcribed regions of mRNA genes, repressing internal cryptic promoters and slowing elongation. Here we explore the function of this pathway by analysing transcription in yeast undergoing a series of carbon source shifts. Approximately 80 mRNA genes show increased induction upon SET2 deletion. A majority of these promoters have overlapping lncRNA transcription that targets H3K36me3 and deacetylation by Rpd3S to the mRNA promoter. We previously reported a similar mechanism for H3K4me2-mediated repression via recruitment of the Set3C histone deacetylase. Here we show that the distance between an mRNA and overlapping lncRNA promoter determines whether Set2-Rpd3S or Set3C represses. This analysis also reveals many previously unreported cryptic ncRNAs induced by specific carbon sources, showing that cryptic promoters can be environmentally regulated. Therefore, in addition to repression of cryptic transcription and modulation of elongation, H3K36 methylation maintains optimal expression dynamics of many mRNAs and ncRNAs. © The Author(s) 2016.
URI
http://hdl.handle.net/20.500.11750/2122
DOI
10.1038/ncomms13534
Publisher
Nature Publishing Group
Related Researcher
  • 이성배 Lee, Sung Bae
  • Research Interests Cellular mechanism of neurodegenerative diseases; Neuronal maintenance and remodeling; 퇴행성 뇌질환의 세포기전; 신경계 유지 및 리모델링 연구
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10.1038_ncomms13534.pdf

10.1038_ncomms13534.pdf

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Appears in Collections:
Department of Brain Sciences Laboratory of Neurodegenerative Diseases and Aging 1. Journal Articles

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