Evidence map›Paper›PMID 38934859›Full record

ArticleGenome biology and evolution2024

High Polymorphism Levels of De Novo ORFs in a Yoruba Human Population.

Covadonga Vara, José Carlos Montañés, M Mar Albà

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Article in Genome biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Covadonga VaraResearch Programme on Biomedical Informatics (GRIB),Hospital del Mar Research Institute, Barcelona, Spain.ORCID 0000-0002-8264-9262
José Carlos MontañésResearch Programme on Biomedical Informatics (GRIB),Hospital del Mar Research Institute, Barcelona, Spain.ORCID 0000-0001-6453-9847
M Mar AlbàResearch Programme on Biomedical Informatics (GRIB),Hospital del Mar Research Institute, Barcelona, Spain.ORCID 0000-0002-7963-7375

Funding

canERDFEuropean Research Council 101052538European Union 2021SGR00042Generalitat de Catalunyanor
6 · The paper itself

Abstract

During evolution, new open reading frames (ORFs) with the potential to give rise to novel proteins continuously emerge. A recent compilation of noncanonical ORFs with translation signatures in humans has identified thousands of cases with a putative de novo origin. However, it is not known which is their distribution in the population. Are they universally translated? Here, we use ribosome profiling data from 65 lymphoblastoid cell lines from individuals of Yoruba origin to investigate this question. We identify 2,587 de novo ORFs translated in at least one of the cell lines. In line with their de novo origin, the encoded proteins tend to be smaller than 100 amino acids and encode positively charged proteins. We observe that the de novo ORFs are more polymorphic in the population than the set of canonical proteins, with a substantial fraction of them being translated in only some of the cell lines. Remarkably, this difference remains significant after controlling for differences in the translation levels. These results suggest that variations in the level translation of de novo ORFs could be a relevant source of intraspecies phenotypic diversity in humans.

Indexed as

Open Reading FramesPolymorphism, GeneticCell LineEvolution, MolecularHumansProtein BiosynthesisRibosomesde novo ORFhumanLCLpolymorphismtranslation

Identifiers

PMID38934859
PMCPMC11221430

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.