A community-driven roadmap to advance research on translated open reading frames detected by Ribo-seq

Author:

Mudge Jonathan M.ORCID,Ruiz-Orera JorgeORCID,Prensner John R.ORCID,Brunet Marie A.ORCID,Gonzalez Jose ManuelORCID,Magrane MicheleORCID,Martinez ThomasORCID,Schulz Jana FelicitasORCID,Yang Yucheng T.ORCID,Albà M. MarORCID,Baranov Pavel V.ORCID,Bazzini ArielORCID,Bruford ElspethORCID,Martin Maria JesusORCID,Carvunis Anne-RuxandraORCID,Chen JinORCID,Couso Juan PabloORCID,Flicek PaulORCID,Frankish AdamORCID,Gerstein MarkORCID,Hubner NorbertORCID,Ingolia Nicholas T.ORCID,Menschaert GerbenORCID,Ohler UweORCID,Roucou XavierORCID,Saghatelian AlanORCID,Weissman JonathanORCID,van Heesch SebastiaanORCID

Abstract

ABSTRACTRibosome profiling (Ribo-seq) has catalyzed a paradigm shift in our understanding of the translational ‘vocabulary’ of the human genome, discovering thousands of translated open reading frames (ORFs) within long non-coding RNAs and presumed untranslated regions of protein-coding genes. However, reference gene annotation projects have been circumspect in their incorporation of these ORFs due to uncertainties about their experimental reproducibility and physiological roles. Yet, it is indisputable that certain Ribo-seq ORFs make stable proteins, others mediate gene regulation, and many have medical implications. Ultimately, the absence of standardized ORF annotation has created a circular problem: while Ribo-seq ORFs remain unannotated by reference biological databases, this lack of characterisation will thwart research efforts examining their roles. Here, we outline the initial stages of a community-led effort supported by GENCODE / Ensembl, HGNC and UniProt to produce a consolidated catalog of human Ribo-seq ORFs.

Publisher

Cold Spring Harbor Laboratory

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