Street Lena, Rothamel Katherine, Brannan Kristopher, Jin Wenhao, Bokor Benjamin, Dong Kevin, Rhine Kevin, Madrigal Assael, Al-Azzam Norah, Kim Jenny Kim, Ma Yanzhe, Abdou Ahmed, Wolin Erica, Doron-Mandel Ella, Ahdout Joshua, Mujumdar Mayuresh, Jovanovic Marko, Yeo Gene W
These authors contributed equally.
Department of Biological Sciences, Columbia University, New York, NY, USA.
bioRxiv. 2023 Jun 8:2023.06.08.544225. doi: 10.1101/2023.06.08.544225.
Messenger RNAs (mRNAs) interact with RNA-binding proteins (RBPs) in diverse ribonucleoprotein complexes (RNPs) during distinct life-cycle stages for their processing and maturation. While substantial attention has focused on understanding RNA regulation by assigning proteins, particularly RBPs, to specific RNA substrates, there has been considerably less exploration leveraging protein-protein interaction (PPI) methodologies to identify and study the role of proteins in mRNA life-cycle stages. To address this gap, we generated an RNA-aware RBP-centric PPI map across the mRNA life-cycle by immunopurification (IP-MS) of ~100 endogenous RBPs across the life-cycle in the presence or absence of RNase, augmented by size exclusion chromatography (SEC-MS). Aside from confirming 8,700 known and discovering 20,359 novel interactions between 1125 proteins, we determined that 73% of our IP interactions are regulated by the presence of RNA. Our PPI data enables us to link proteins to life-cycle stage functions, highlighting that nearly half of the proteins participate in at least two distinct stages. We show that one of the most highly interconnected proteins, ERH, engages in multiple RNA processes, including via interactions with nuclear speckles and the mRNA export machinery. We also demonstrate that the spliceosomal protein SNRNP200 participates in distinct stress granule-associated RNPs and occupies different RNA target regions in the cytoplasm during stress. Our comprehensive RBP-focused PPI network is a novel resource for identifying multi-stage RBPs and exploring RBP complexes in RNA maturation.
信使核糖核酸(mRNA)在不同的生命周期阶段与多种核糖核蛋白复合物(RNP)中的RNA结合蛋白(RBP)相互作用,以进行加工和成熟。虽然大量研究集中在通过将蛋白质(特别是RBP)与特定RNA底物进行匹配来理解RNA调控,但利用蛋白质-蛋白质相互作用(PPI)方法来识别和研究蛋白质在mRNA生命周期阶段中的作用的探索却少得多。为了填补这一空白,我们通过在有或没有核糖核酸酶的情况下,对整个生命周期中的约100种内源性RBP进行免疫纯化(IP-MS),并辅以尺寸排阻色谱法(SEC-MS),生成了一个贯穿mRNA生命周期的以RNA感知的RBP为中心的PPI图谱。除了确认8700种已知相互作用并发现1125种蛋白质之间的20359种新相互作用外,我们还确定我们的IP相互作用中有73%受RNA的存在调控。我们的PPI数据使我们能够将蛋白质与生命周期阶段功能联系起来,突出显示近一半的蛋白质参与至少两个不同阶段。我们表明,相互连接程度最高的蛋白质之一ERH参与多种RNA过程,包括通过与核斑点和mRNA输出机制的相互作用。我们还证明,剪接体蛋白SNRNP200参与不同的应激颗粒相关RNP,并在应激期间在细胞质中占据不同的RNA靶区域。我们全面的以RBP为重点的PPI网络是识别多阶段RBP和探索RNA成熟过程中RBP复合物的新资源。