Duffy Erin E, Assad Elena G, Kalish Brian T, Greenberg Michael E
Department of Neurobiology, Harvard Medical School, Boston, MA, United States.
Program in Neuroscience and Mental Health, SickKids Research Institute, Toronto, ON, Canada.
Front Mol Neurosci. 2024 May 14;17:1386219. doi: 10.3389/fnmol.2024.1386219. eCollection 2024.
The mammalian central nervous system coordinates a network of signaling pathways and cellular interactions, which enable a myriad of complex cognitive and physiological functions. While traditional efforts to understand the molecular basis of brain function have focused on well-characterized proteins, recent advances in high-throughput translatome profiling have revealed a staggering number of proteins translated from non-canonical open reading frames (ncORFs) such as 5' and 3' untranslated regions of annotated proteins, out-of-frame internal ORFs, and previously annotated non-coding RNAs. Of note, microproteins < 100 amino acids (AA) that are translated from such ncORFs have often been neglected due to computational and biochemical challenges. Thousands of putative microproteins have been identified in cell lines and tissues including the brain, with some serving critical biological functions. In this perspective, we highlight the recent discovery of microproteins in the brain and describe several hypotheses that have emerged concerning microprotein function in the developing and mature nervous system.
哺乳动物的中枢神经系统协调着一个信号通路和细胞相互作用的网络,这些信号通路和细胞相互作用使得无数复杂的认知和生理功能得以实现。虽然传统上理解脑功能分子基础的努力主要集中在特征明确的蛋白质上,但高通量翻译组分析的最新进展揭示了从非规范开放阅读框(ncORFs)翻译而来的大量蛋白质,如注释蛋白质的5'和3'非翻译区、移码内部开放阅读框以及先前注释的非编码RNA。值得注意的是,由于计算和生化方面的挑战,从这些ncORFs翻译而来的小于100个氨基酸(AA)的微蛋白常常被忽视。在包括大脑在内的细胞系和组织中已经鉴定出数千种假定的微蛋白,其中一些具有关键的生物学功能。从这个角度来看,我们强调了最近在大脑中发现的微蛋白,并描述了关于微蛋白在发育中和成熟神经系统中功能的几种假说。