Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724.
Graduate Program in Molecular and Cellular Biology, Stony Brook University, Stony Brook, NY 11794.
Proc Natl Acad Sci U S A. 2024 May 21;121(21):e2322974121. doi: 10.1073/pnas.2322974121. Epub 2024 May 14.
SRSF1 is the founding member of the SR protein family. It is required-interchangeably with other SR proteins-for pre-mRNA splicing in vitro, and it regulates various alternative splicing events. Dysregulation of SRSF1 expression contributes to cancer and other pathologies. Here, we characterized SRSF1's interactome using proximity labeling and mass spectrometry. This approach yielded 190 proteins enriched in the SRSF1 samples, independently of the N- or C-terminal location of the biotin-labeling domain. The detected proteins reflect established functions of SRSF1 in pre-mRNA splicing and reveal additional connections to spliceosome proteins, in addition to other recently identified functions. We validated a robust interaction with the spliceosomal RNA helicase DDX23/PRP28 using bimolecular fluorescence complementation and in vitro binding assays. The interaction is mediated by the N-terminal RS-like domain of DDX23 and both RRM1 and the RS domain of SRSF1. During pre-mRNA splicing, DDX23's ATPase activity is essential for the pre-B to B spliceosome complex transition and for release of U1 snRNP from the 5' splice site. We show that the RS-like region of DDX23's N-terminal domain is important for spliceosome incorporation, while larger deletions in this domain alter subnuclear localization. We discuss how the identified interaction of DDX23 with SRSF1 and other SR proteins may be involved in the regulation of these processes.
SRSF1 是 SR 蛋白家族的创始成员。它与其他 SR 蛋白一起,在体外剪接前 mRNA 是必需的,并且它调节各种选择性剪接事件。SRSF1 表达的失调导致癌症和其他病理学。在这里,我们使用邻近标记和质谱法对 SRSF1 的相互作用组进行了表征。这种方法产生了 190 种在 SRSF1 样品中富集的蛋白质,而与生物素标记结构域的 N 或 C 末端位置无关。检测到的蛋白质反映了 SRSF1 在 pre-mRNA 剪接中的既定功能,并揭示了与剪接体蛋白的其他额外连接,以及其他最近确定的功能。我们使用双分子荧光互补和体外结合测定验证了与剪接体 RNA 解旋酶 DDX23/PRP28 的稳健相互作用。这种相互作用是由 DDX23 的 N 端 RS 样结构域以及 SRSF1 的两个 RRM1 和 RS 结构域介导的。在 pre-mRNA 剪接过程中,DDX23 的 ATP 酶活性对于 pre-B 到 B 剪接体复合物的转变以及 U1 snRNP 从 5' 剪接位点的释放是必需的。我们表明,DDX23 的 N 端结构域的 RS 样区域对于剪接体的掺入很重要,而该结构域中的较大缺失会改变亚核定位。我们讨论了 DDX23 与 SRSF1 和其他 SR 蛋白的鉴定相互作用如何参与这些过程的调节。