Makarewich Catherine A, Olson Eric N
Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Hamon Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Hamon Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Trends Cell Biol. 2017 Sep;27(9):685-696. doi: 10.1016/j.tcb.2017.04.006. Epub 2017 May 18.
Advances in computational biology and large-scale transcriptome analyses have revealed that a much larger portion of the genome is transcribed than was previously recognized, resulting in the production of a diverse population of RNA molecules with both protein-coding and noncoding potential. Emerging evidence indicates that several RNA molecules have been mis-annotated as noncoding and in fact harbor short open reading frames (sORFs) that encode functional peptides and that have evaded detection until now due to their small size. sORF-encoded peptides (SEPs), or micropeptides, have been shown to have important roles in fundamental biological processes and in the maintenance of cellular homeostasis. These small proteins can act independently, for example as ligands or signaling molecules, or they can exert their biological functions by engaging with and modulating larger regulatory proteins. Given their small size, micropeptides may be uniquely suited to fine-tune complex biological systems.
计算生物学和大规模转录组分析的进展表明,基因组中被转录的部分比以前认为的要大得多,从而产生了具有蛋白质编码和非编码潜力的多种RNA分子群体。新出现的证据表明,一些RNA分子被错误地注释为非编码RNA,实际上含有短开放阅读框(sORF),这些短开放阅读框编码功能性肽,并且由于其尺寸小,至今仍未被检测到。短开放阅读框编码的肽(SEP)或微肽已被证明在基本生物学过程和细胞稳态维持中具有重要作用。这些小蛋白可以独立发挥作用,例如作为配体或信号分子,或者它们可以通过与更大的调节蛋白结合并调节它们来发挥生物学功能。鉴于其小尺寸,微肽可能特别适合微调复杂的生物系统。