| Literature DB >> 33468658 |
Minseob Koh1,2, Insha Ahmad1, Yeonjin Ko1, Yuxiang Zhang1, Thomas F Martinez3, Jolene K Diedrich3, Qian Chu3, James J Moresco3, Michael A Erb1, Alan Saghatelian4, Peter G Schultz5, Michael J Bollong5.
Abstract
Recent technological advances have expanded the annotated protein coding content of mammalian genomes, as hundreds of previously unidentified, short open reading frame (ORF)-encoded peptides (SEPs) have now been found to be translated. Although several studies have identified important physiological roles for this emerging protein class, a general method to define their interactomes is lacking. Here, we demonstrate that genetic incorporation of the photo-crosslinking noncanonical amino acid AbK into SEP transgenes allows for the facile identification of SEP cellular interaction partners using affinity-based methods. From a survey of seven SEPs, we report the discovery of short ORF-encoded histone binding protein (SEHBP), a conserved microprotein that interacts with chromatin-associated proteins, localizes to discrete genomic loci, and induces a robust transcriptional program when overexpressed in human cells. This work affords a straightforward method to help define the physiological roles of SEPs and demonstrates its utility by identifying SEHBP as a short ORF-encoded transcription factor.Entities:
Keywords: expanded genetic code; photo-crosslinking; short open reading frame-encoded peptide; transcriptional regulation
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Year: 2021 PMID: 33468658 PMCID: PMC7848545 DOI: 10.1073/pnas.2021943118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 12.779