Chemical Biology Institute, Yale University, West Haven, CT 06516, USA.
Mol Omics. 2019 Apr 1;15(2):108-116. doi: 10.1039/c8mo00283e. Epub 2019 Feb 27.
Small open reading frames (smORFs) encoding polypeptides of less than 100 amino acids in eukaryotes (50 amino acids in prokaryotes) were historically excluded from genome annotation. However, recent advances in genomics, ribosome footprinting, and proteomics have revealed thousands of translated smORFs in genomes spanning evolutionary space. These smORFs can encode functional polypeptides, or act as cis-translational regulators. Herein we review evidence that some smORF-encoded polypeptides (SEPs) participate in stress responses in both prokaryotes and eukaryotes, and that some upstream ORFs (uORFs) regulate stress-responsive translation of downstream cistrons in eukaryotic cells. These studies provide insight into a regulated subclass of smORFs and suggest that at least some SEPs may participate in maintenance of cellular homeostasis under stress.
真核生物中的小开放阅读框(smORFs)编码小于 100 个氨基酸的多肽(原核生物中的 50 个氨基酸)在历史上被排除在基因组注释之外。然而,基因组学、核糖体足迹和蛋白质组学的最新进展揭示了跨越进化空间的基因组中数千个翻译的 smORFs。这些 smORFs 可以编码功能性多肽,或者作为顺反翻译调节因子。本文综述了一些证据表明,一些 smORF 编码的多肽(SEPs)参与原核生物和真核生物的应激反应,一些上游 ORF(uORF)调节真核细胞中下游顺式基因座的应激响应翻译。这些研究为调控的 smORF 亚类提供了线索,并表明至少一些 SEP 可能参与应激下细胞内稳态的维持。