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Ess2 通过不同的相互作用结构域连接转录调节因子和剪接体复合物。

Ess2 bridges transcriptional regulators and spliceosomal complexes via distinct interacting domains.

作者信息

Takada Ichiro, Tsuchiya Megumi, Yanaka Kaori, Hidano Shinya, Takahashi Sayuri, Kobayashi Takashi, Ogawa Hidesato, Nakagawa Sinichi, Makishima Makoto

机构信息

Division of Biochemistry, Department of Biomedical Sciences, School of Medicine, Nihon University, Itabashi-ku, Tokyo 173-8610, Japan.

Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita 565-0871, Japan.

出版信息

Biochem Biophys Res Commun. 2018 Mar 4;497(2):597-604. doi: 10.1016/j.bbrc.2018.02.110. Epub 2018 Feb 16.

Abstract

Transcription and pre-mRNA splicing are complex, coupled processes that involve transcriptional co-regulators. Ess2 (also termed Dgcr14) is a nuclear protein that enhances the transcriptional activity of retinoic acid receptor-related orphan receptor gamma/gamma-t (Rorγ/γt). Ess2 is also a component of the spliceosomal C complex (containing U2, U5 and U6 snRNAs). However, the domains in Ess2 that function in splicing and transcription have not been identified. To elucidate the roles of Ess2 in splicing and transcription, we performed RNA immunoprecipitation (RIP) assays to detect Ess2-interacting snRNAs. We found that Ess2 associated with U6 snRNA as well as U1 and U4 snRNAs. Experiments using Ess2 deletion mutants showed that a C-terminus deletion mutant of Ess2 (1-399 a. a.) lost its ability to associate with snRNAs, whereas the N-terminus domain of Ess2 (1-200 a. a.) associated with Rorγ/γt, but not with snRNAs. Interestingly, experiments using anti-ROR common antibody showed that Rors also associated with U4 and U6 snRNAs. Ess2 knockdown in a T cell hybridoma (68-41 cells) abrogated the interaction between spliceosomes and Rors. An Ess2-dependent association was also found between an lncRNA (Rmrp) and Rors. We thus propose that Ess2 associates with both transcriptional factors and spliceosomal complexes and modulates splicing reactions coupled with transcription factors.

摘要

转录和前体mRNA剪接是复杂的、相互偶联的过程,涉及转录共调节因子。Ess2(也称为Dgcr14)是一种核蛋白,可增强视黄酸受体相关孤儿受体γ/γt(Rorγ/γt)的转录活性。Ess2也是剪接体C复合物(包含U2、U5和U6 snRNA)的一个组分。然而,Ess2中在剪接和转录中发挥作用的结构域尚未确定。为了阐明Ess2在剪接和转录中的作用,我们进行了RNA免疫沉淀(RIP)试验以检测与Ess2相互作用的snRNA。我们发现Ess2与U6 snRNA以及U1和U4 snRNA相关联。使用Ess2缺失突变体的实验表明,Ess2的C末端缺失突变体(1 - 399个氨基酸)失去了与snRNA相关联的能力,而Ess2的N末端结构域(1 - 200个氨基酸)与Rorγ/γt相关联,但不与snRNA相关联。有趣的是,使用抗ROR通用抗体的实验表明,Rors也与U4和U6 snRNA相关联。在T细胞杂交瘤(68 - 41细胞)中敲低Ess2消除了剪接体与Rors之间的相互作用。在长链非编码RNA(Rmrp)和Rors之间也发现了一种Ess2依赖性关联。因此,我们提出Ess2与转录因子和剪接体复合物都相关联,并调节与转录因子偶联在一起的剪接反应。

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