Suppr超能文献

蛋白质相互作用网络分析揭示了Prp19剪接因子在含内含子基因和无内含子基因转录中的作用。

Protein-interaction network analysis reveals a role of Prp19 splicing factor in transcription of both intron-containing and intron-lacking genes.

作者信息

Dwyer Katherine, Essak Mary-Ann, Awada Ahlam, Dhoondia Zuzer, Ansari Athar

出版信息

bioRxiv. 2025 Apr 1:2025.03.31.646471. doi: 10.1101/2025.03.31.646471.

Abstract

We have previously demonstrated that the transcription-dependent interaction of the promoter and terminator ends of a gene, which results in the formation of a gene loop, is facilitated by the interaction of the general transcription factor TFIIB with the CF1, CPF and Rat1 termination complexes. To further elucidate the protein-protein interactions that stabilize gene loop, we performed mass spectrometry of affinity purified termination complexes from chromatin fraction. Quantitative proteomic analysis revealed additional interactions of termination factors with TFIID and SAGA complex. Since gene looping of intron-containing genes involves additional contacts of the promoter and terminator with the intron, we examined if termination factors interact with the splicing factors as well. All three termination complexes displayed statistically significant interactions with Prp19, Prp43, Sub2, Snu114, Brr2 and Smb1 splicing factors. Since Prp43 and Prp19 consistently emerged as the interactor of both initiation and termination factors, we affinity-purified both and performed mass spectrometry. Prp19 exhibited interactions with subunits of TFIID, CPF complex, and the RSC chromatin remodeling complex. These interactions were observed exclusively in the chromatin context, thereby implicating the factor in transcription of protein coding genes. Since fewer than 4% of yeast genes contain introns, we hypothesized that Prp19 might have a broader role in RNAPII transcription cycle. Auxin-mediated depletion of Prp19 resulted in about two-fold decrease in transcription of a subset of both intron-containing and intron-lacking genes. Specifically, the promoter recruitment of TBP registered a significant decline in the absence of Prp19. Chromatin immunoprecipitation (ChIP) analysis revealed crosslinking of Prp19 to the promoter proximal as well as downstream regions of both intronic and non-intronic genes. These findings demonstrate that Prp19 has a novel role in the initiation step of transcription in yeast.

摘要

我们之前已经证明,基因启动子和终止子末端之间的转录依赖性相互作用会导致基因环的形成,而通用转录因子TFIIB与CF1、CPF和Rat1终止复合物的相互作用促进了这种相互作用。为了进一步阐明稳定基因环的蛋白质-蛋白质相互作用,我们对从染色质部分亲和纯化的终止复合物进行了质谱分析。定量蛋白质组学分析揭示了终止因子与TFIID和SAGA复合物的其他相互作用。由于含内含子基因的基因环化涉及启动子和终止子与内含子的额外接触,我们研究了终止因子是否也与剪接因子相互作用。所有三种终止复合物都与Prp19、Prp43、Sub2、Snu114、Brr2和Smb1剪接因子表现出统计学上显著的相互作用。由于Prp43和Prp19一直作为起始因子和终止因子的相互作用分子出现,我们对两者进行了亲和纯化并进行了质谱分析。Prp19与TFIID的亚基、CPF复合物和RSC染色质重塑复合物表现出相互作用。这些相互作用仅在染色质环境中观察到,从而表明该因子参与蛋白质编码基因的转录。由于酵母基因中只有不到4%含有内含子,我们推测Prp19可能在RNA聚合酶II转录周期中发挥更广泛的作用。生长素介导的Prp19缺失导致含内含子和不含内含子基因子集的转录下降约两倍。具体而言,在没有Prp19的情况下,TBP在启动子处的募集显著下降。染色质免疫沉淀(ChIP)分析揭示了Prp19与内含子和非内含子基因的启动子近端以及下游区域的交联。这些发现表明Prp19在酵母转录起始步骤中具有新的作用。

相似文献

10
Gene Architecture Facilitates Intron-Mediated Enhancement of Transcription.基因结构促进内含子介导的转录增强。
Front Mol Biosci. 2021 Apr 21;8:669004. doi: 10.3389/fmolb.2021.669004. eCollection 2021.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验