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酵母剪接因子Fyv6对3'剪接位点选择的调控

Control of 3' splice site selection by the yeast splicing factor Fyv6.

作者信息

Senn Katherine A, Lipinski Karli A, Zeps Natalie J, Griffin Amory F, Wilkinson Max E, Hoskins Aaron A

机构信息

Department of Biochemistry, University of Wisconsin-Madison, Madison, United States.

Department of Chemistry, University of Wisconsin-Madison, Madison, United States.

出版信息

Elife. 2024 Dec 17;13:RP100449. doi: 10.7554/eLife.100449.

Abstract

Pre-mRNA splicing is catalyzed in two steps: 5' splice site (SS) cleavage and exon ligation. A number of proteins transiently associate with spliceosomes to specifically impact these steps (first and second step factors). We recently identified Fyv6 (FAM192A in humans) as a second step factor in ; however, we did not determine how widespread Fyv6's impact is on the transcriptome. To answer this question, we have used RNA sequencing (RNA-seq) to analyze changes in splicing. These results show that loss of Fyv6 results in activation of non-consensus, branch point (BP) proximal 3' SS transcriptome-wide. To identify the molecular basis of these observations, we determined a high-resolution cryo-electron microscopy (cryo-EM) structure of a yeast product complex spliceosome containing Fyv6 at 2.3 Å. The structure reveals that Fyv6 is the only second step factor that contacts the Prp22 ATPase and that Fyv6 binding is mutually exclusive with that of the first step factor Yju2. We then use this structure to dissect Fyv6 functional domains and interpret results of a genetic screen for suppressor mutations. The combined transcriptomic, structural, and genetic studies allow us to propose a model in which Yju2/Fyv6 exchange facilitates exon ligation and Fyv6 promotes usage of consensus, BP distal 3' SS.

摘要

前体mRNA剪接分两步进行催化:5'剪接位点(SS)切割和外显子连接。许多蛋白质与剪接体瞬时结合,以特异性影响这些步骤(第一步和第二步因子)。我们最近将Fyv6(人类中的FAM192A)鉴定为第二步因子;然而,我们尚未确定Fyv6对转录组的影响有多广泛。为了回答这个问题,我们使用RNA测序(RNA-seq)来分析剪接变化。这些结果表明,Fyv6的缺失导致全转录组范围内非共识、分支点(BP)近端3' SS的激活。为了确定这些观察结果的分子基础,我们确定了一个含有Fyv6的酵母产物复合剪接体在2.3 Å分辨率下的高分辨率冷冻电子显微镜(cryo-EM)结构。该结构表明,Fyv6是唯一与Prp22 ATP酶接触的第二步因子,并且Fyv6的结合与第一步因子Yju2的结合相互排斥。然后,我们利用这个结构剖析Fyv6功能域,并解释抑制突变基因筛选的结果。综合的转录组学、结构和遗传学研究使我们能够提出一个模型,其中Yju2/Fyv6交换促进外显子连接,而Fyv6促进共识、BP远端3' SS的使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25c4/11651659/ac897766d2a3/elife-100449-fig1.jpg

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