The Cryptic Bacterial Microproteome

Abstract

Microproteins encoded by small open reading frames (smORFs) comprise the "dark matter" of proteomes. Although functional microproteins were identified in diverse organisms from all three domains of life, bacterial smORFs remain poorly characterized. In this comprehensive study of intergenic smORFs (ismORFs, 15-70 codons) in 5,668 bacterial genomes of the family Enterobacteriaceae, we identified 67,297 clusters of ismORFs subject to purifying selection. The ismORFs mainly code for hydrophobic, potentially transmembrane, unstructured, or minimally structured microproteins. Using AlphaFold Multimer, we predicted interactions of some of the predicted microproteins encoded by transcribed ismORFs with proteins encoded by neighboring genes, revealing the potential of microproteins to regulate the activity of various proteins, particularly, under stress. We compiled a catalog of predicted microprotein families with different levels of evidence from synteny analysis, structure prediction, and transcription and translation data. This study offers a resource for investigation of biological functions of microproteins. HighlightsO_LIThousands of previously unknown bacterial microproteins predicted C_LIO_LIMost microproteins belong to lineage-specific families, revealing unexplored diversity of bacterial proteomes C_LIO_LIComparative genome analysis suggests de novo emergence of numerous microproteins C_LIO_LIInteractions between stress-induced microproteins and known functional proteins predicted C_LIO_LIThis study provides a resource to investigate cryptic bacterial microproteomes C_LI