European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Collaboration for joint Ph.D. degree between EMBL and Heidelberg University, Faculty of Biosciences, Heidelberg, Germany.
RNA. 2022 May;28(5):742-755. doi: 10.1261/rna.079129.122. Epub 2022 Feb 24.
Cellular processes can be regulated at multiple levels, including transcriptional, post-transcriptional, and post-translational mechanisms. We have recently shown that the small, noncoding vault RNA1-1 negatively riboregulates p62 oligomerization in selective autophagy through direct interaction with the autophagic receptor. This function is highly specific for this Pol III transcript, but the determinants of this specificity and a mechanistic explanation of how vault RNA1-1 inhibits p62 oligomerization are lacking. Here, we combine biochemical and functional experiments to answer these questions. We show that the PB1 domain and adjacent linker region of p62 (aa 1-122) are necessary and sufficient for specific vault RNA1-1 binding, and we identify lysine 7 and arginine 21 as key hinges for p62 riboregulation. Chemical structure probing of vault RNA1-1 further reveals a central flexible loop within vault RNA1-1 that is required for the specific interaction with p62. Overall, our data provide molecular insight into how a small RNA riboregulates protein-protein interactions critical to the activation of specific autophagy.
细胞过程可以在多个水平上进行调节,包括转录、转录后和翻译后机制。我们最近表明,小的非编码 vault RNA1-1 通过与自噬受体的直接相互作用,负调控选择性自噬中的 p62 寡聚化。该功能高度特异于该 Pol III 转录物,但特异性的决定因素以及 vault RNA1-1 如何抑制 p62 寡聚化的机制解释尚不清楚。在这里,我们结合生化和功能实验来回答这些问题。我们表明,p62(aa 1-122)的 PB1 结构域和相邻的连接区是与 vault RNA1-1 特异性结合所必需和充分的,并且我们鉴定出赖氨酸 7 和精氨酸 21 是 p62 核糖调控的关键铰链。对 vault RNA1-1 的化学结构探测进一步揭示了 vault RNA1-1 中的中央柔性环,该环是与 p62 特异性相互作用所必需的。总的来说,我们的数据提供了分子见解,说明小分子 RNA 如何调节对特定自噬的激活至关重要的蛋白质-蛋白质相互作用。