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基础转录复合体成分TAF3将核磷酸肌醇的变化转化为转录输出。

The basal transcription complex component TAF3 transduces changes in nuclear phosphoinositides into transcriptional output.

作者信息

Stijf-Bultsma Yvette, Sommer Lilly, Tauber Maria, Baalbaki Mai, Giardoglou Panagiota, Jones David R, Gelato Kathy A, van Pelt Jason, Shah Zahid, Rahnamoun Homa, Toma Clara, Anderson Karen E, Hawkins Philip, Lauberth Shannon M, Haramis Anna-Pavlina G, Hart Daniel, Fischle Wolfgang, Divecha Nullin

机构信息

The Inositide Laboratory, Centre for Biological Sciences, Highfield Campus, University of Southampton, Southampton SO171BJ, UK; The Inositide Laboratory, the CRUK Manchester Institute, the University of Manchester, Wilmslow Road, Manchester M204BX, UK.

The Inositide Laboratory, the CRUK Manchester Institute, the University of Manchester, Wilmslow Road, Manchester M204BX, UK.

出版信息

Mol Cell. 2015 May 7;58(3):453-67. doi: 10.1016/j.molcel.2015.03.009. Epub 2015 Apr 9.

Abstract

Phosphoinositides (PI) are important signaling molecules in the nucleus that influence gene expression. However, if and how nuclear PI directly affects the transcriptional machinery is not known. We report that the lipid kinase PIP4K2B regulates nuclear PI5P and the expression of myogenic genes during myoblast differentiation. A targeted screen for PI interactors identified the PHD finger of TAF3, a TATA box binding protein-associated factor with important roles in transcription regulation, pluripotency, and differentiation. We show that the PI interaction site is distinct from the known H3K4me3 binding region of TAF3 and that PI binding modulates association of TAF3 with H3K4me3 in vitro and with chromatin in vivo. Analysis of TAF3 mutants indicates that TAF3 transduces PIP4K2B-mediated alterations in PI into changes in specific gene transcription. Our study reveals TAF3 as a direct target of nuclear PI and further illustrates the importance of basal transcription components as signal transducers.

摘要

磷酸肌醇(PI)是细胞核中影响基因表达的重要信号分子。然而,核PI是否以及如何直接影响转录机制尚不清楚。我们报告,脂质激酶PIP4K2B在成肌细胞分化过程中调节核PI5P和肌源性基因的表达。对PI相互作用分子的靶向筛选鉴定出TAF3的PHD结构域,TAF3是一种与TATA盒结合蛋白相关的因子,在转录调控、多能性和分化中起重要作用。我们表明,PI相互作用位点与TAF3已知的H3K4me3结合区域不同,并且PI结合在体外调节TAF3与H3K4me3的结合以及在体内调节TAF3与染色质的结合。对TAF3突变体的分析表明,TAF3将PIP4K2B介导的PI变化转化为特定基因转录的变化。我们的研究揭示TAF3是核PI的直接靶点,并进一步说明了基础转录成分作为信号转导分子的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77f8/4429956/8d75f4e57b31/fx1.jpg

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