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H3K36甲基化通过增强转录保真度调控酿酒酵母中的营养应激反应。

H3K36 Methylation Regulates Nutrient Stress Response in Saccharomyces cerevisiae by Enforcing Transcriptional Fidelity.

作者信息

McDaniel Stephen L, Hepperla Austin J, Huang Jie, Dronamraju Raghuvar, Adams Alexander T, Kulkarni Vidyadhar G, Davis Ian J, Strahl Brian D

机构信息

Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Biochemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Cell Rep. 2017 Jun 13;19(11):2371-2382. doi: 10.1016/j.celrep.2017.05.057.

Abstract

Set2-mediated histone methylation at H3K36 regulates diverse activities, including DNA repair, mRNA splicing, and suppression of inappropriate (cryptic) transcription. Although failure of Set2 to suppress cryptic transcription has been linked to decreased lifespan, the extent to which cryptic transcription influences other cellular functions is poorly understood. Here, we uncover a role for H3K36 methylation in the regulation of the nutrient stress response pathway. We found that the transcriptional response to nutrient stress was dysregulated in SET2-deleted (set2Δ) cells and was correlated with genome-wide bi-directional cryptic transcription that originated from within gene bodies. Antisense transcripts arising from these cryptic events extended into the promoters of the genes from which they arose and were associated with decreased sense transcription under nutrient stress conditions. These results suggest that Set2-enforced transcriptional fidelity is critical to the proper regulation of inducible and highly regulated transcription programs.

摘要

Set2介导的H3K36组蛋白甲基化调控多种活动,包括DNA修复、mRNA剪接以及抑制不适当(隐蔽)转录。尽管Set2无法抑制隐蔽转录与寿命缩短有关,但隐蔽转录对其他细胞功能的影响程度仍知之甚少。在此,我们揭示了H3K36甲基化在营养应激反应途径调控中的作用。我们发现,在缺失SET2(set2Δ)的细胞中,对营养应激的转录反应失调,且与源自基因体内的全基因组双向隐蔽转录相关。这些隐蔽事件产生的反义转录本延伸至其产生基因的启动子区域,并与营养应激条件下正义转录的减少相关。这些结果表明,Set2维持的转录保真度对于诱导型且高度受调控的转录程序的正确调控至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa64/5528882/3b6a96aaccc9/nihms880075f1.jpg

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本文引用的文献

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Shaping the cellular landscape with Set2/SETD2 methylation.通过Set2/SETD2甲基化塑造细胞格局。
Cell Mol Life Sci. 2017 Sep;74(18):3317-3334. doi: 10.1007/s00018-017-2517-x. Epub 2017 Apr 6.
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Protein Abundance Control by Non-coding Antisense Transcription.非编码反义转录对蛋白质丰度的调控
Cell Rep. 2016 Jun 21;15(12):2625-36. doi: 10.1016/j.celrep.2016.05.043. Epub 2016 Jun 9.
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Histone exchange, chromatin structure and the regulation of transcription.组蛋白交换、染色质结构和转录调控。
Nat Rev Mol Cell Biol. 2015 Mar;16(3):178-89. doi: 10.1038/nrm3941. Epub 2015 Feb 4.

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