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转录共激活因子p300和CBP的基因组占据情况

Genomic occupancy of the transcriptional co-activators p300 and CBP.

作者信息

Holmqvist Per-Henrik, Mannervik Mattias

机构信息

The Wenner-Gren Institute, Developmental Biology, Stockholm University, Arrheniuslaboratories E3, SE-106 91 Stockholm, Sweden.

出版信息

Transcription. 2013 Jan-Feb;4(1):18-23. doi: 10.4161/trns.22601. Epub 2012 Nov 6.

Abstract

The p300 and CBP co-activators are histone acetylases and central regulators of transcription in metazoans. The genomic occupancy of p300/CBP detected by ChIP-seq experiments can be used to identify transcriptional enhancers. However, studies in Drosophila embryos suggest that there is a preference for some transcription factors in directing p300/CBP to the genome. Although p300/CBP occupancy in general correlates with gene activation, they can also be found at silent genomic regions, which does not result in histone acetylation. Polycomb-mediated H3K27me3 is associated with repression, but does not preclude p300/CBP binding. An antagonism between H3K27ac and H3K27me3 indicates that p300/CBP may be involved in switching between repressed and active chromatin states.

摘要

p300和CBP共激活因子是组蛋白乙酰转移酶,也是后生动物转录的核心调节因子。通过ChIP-seq实验检测到的p300/CBP在基因组中的占位可用于识别转录增强子。然而,对果蝇胚胎的研究表明,在引导p300/CBP进入基因组方面,某些转录因子存在偏好性。虽然p300/CBP的占位通常与基因激活相关,但在沉默的基因组区域也能发现它们,这并不会导致组蛋白乙酰化。多梳蛋白介导的H3K27me3与基因抑制有关,但并不排除p300/CBP的结合。H3K27ac和H3K27me3之间的拮抗作用表明,p300/CBP可能参与了染色质抑制状态和激活状态之间的转换。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e615/3644037/ae9d6af675c1/tran-4-18-g1.jpg

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