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Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue

[Image: see text] The existence of nonannotated protein-coding human short open reading frames (sORFs) has been revealed through the direct detection of their sORF-encoded polypeptide (SEP) products. The discovery of novel SEPs increases the size of the genome and the proteome and provides insights...

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Autores principales: Ma, Jiao, Ward, Carl C., Jungreis, Irwin, Slavoff, Sarah A., Schwaid, Adam G., Neveu, John, Budnik, Bogdan A., Kellis, Manolis, Saghatelian, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993966/
https://www.ncbi.nlm.nih.gov/pubmed/24490786
http://dx.doi.org/10.1021/pr401280w
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author Ma, Jiao
Ward, Carl C.
Jungreis, Irwin
Slavoff, Sarah A.
Schwaid, Adam G.
Neveu, John
Budnik, Bogdan A.
Kellis, Manolis
Saghatelian, Alan
author_facet Ma, Jiao
Ward, Carl C.
Jungreis, Irwin
Slavoff, Sarah A.
Schwaid, Adam G.
Neveu, John
Budnik, Bogdan A.
Kellis, Manolis
Saghatelian, Alan
author_sort Ma, Jiao
collection PubMed
description [Image: see text] The existence of nonannotated protein-coding human short open reading frames (sORFs) has been revealed through the direct detection of their sORF-encoded polypeptide (SEP) products. The discovery of novel SEPs increases the size of the genome and the proteome and provides insights into the molecular biology of mammalian cells, such as the prevalent usage of non-AUG start codons. Through modifications of the existing SEP-discovery workflow, we discover an additional 195 SEPs in K562 cells and extend this methodology to identify novel human SEPs in additional cell lines and human tissue for a final tally of 237 new SEPs. These results continue to expand the human genome and proteome and demonstrate that SEPs are a ubiquitous class of nonannotated polypeptides that require further investigation.
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spelling pubmed-39939662015-02-03 Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue Ma, Jiao Ward, Carl C. Jungreis, Irwin Slavoff, Sarah A. Schwaid, Adam G. Neveu, John Budnik, Bogdan A. Kellis, Manolis Saghatelian, Alan J Proteome Res [Image: see text] The existence of nonannotated protein-coding human short open reading frames (sORFs) has been revealed through the direct detection of their sORF-encoded polypeptide (SEP) products. The discovery of novel SEPs increases the size of the genome and the proteome and provides insights into the molecular biology of mammalian cells, such as the prevalent usage of non-AUG start codons. Through modifications of the existing SEP-discovery workflow, we discover an additional 195 SEPs in K562 cells and extend this methodology to identify novel human SEPs in additional cell lines and human tissue for a final tally of 237 new SEPs. These results continue to expand the human genome and proteome and demonstrate that SEPs are a ubiquitous class of nonannotated polypeptides that require further investigation. American Chemical Society 2014-02-03 2014-03-07 /pmc/articles/PMC3993966/ /pubmed/24490786 http://dx.doi.org/10.1021/pr401280w Text en Copyright © 2014 American Chemical Society
spellingShingle Ma, Jiao
Ward, Carl C.
Jungreis, Irwin
Slavoff, Sarah A.
Schwaid, Adam G.
Neveu, John
Budnik, Bogdan A.
Kellis, Manolis
Saghatelian, Alan
Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue
title Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue
title_full Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue
title_fullStr Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue
title_full_unstemmed Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue
title_short Discovery of Human sORF-Encoded Polypeptides (SEPs) in Cell Lines and Tissue
title_sort discovery of human sorf-encoded polypeptides (seps) in cell lines and tissue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993966/
https://www.ncbi.nlm.nih.gov/pubmed/24490786
http://dx.doi.org/10.1021/pr401280w
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