Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential

Detalhes bibliográficos
Autor(a) principal: Pereira, L
Data de Publicação: 2014
Outros Autores: Soares, P, Triska, P, Rito, T, Waerden, Avd, Li, B, Radivojac, P, Samuels, DC
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10216/109251
Resumo: Mitochondrial proteins are coded by nuclear (nDNA) and mitochondrial (mtDNA) genes, implying a complex cross-talk between the two genomes. Here we investigated the diversity displayed in 104 nuclear-coded mitochondrial proteins from 1,092 individuals from the 1000 Genomes dataset, in order to evaluate if these genes are under the effects of purifying selection and how that selection compares with their mitochondrial encoded counterparts. Only the very rare variants (frequency < 0.1%) in these nDNA genes are indistinguishable from a random set from all possible variants in terms of predicted pathogenicity score, but more frequent variants display distinct signs of purifying selection. Comparisons of selection strength indicate stronger selection in the mtDNA genes compared to this set of nDNA genes, accounted for by the high hydrophobicity of the proteins coded by the mtDNA. Most of the predicted pathogenic variants in the nDNA genes were restricted to a single continental population. The proportion of individuals having at least one potential pathogenic mutation in this gene set was significantly lower in Europeans than in Africans and Asians. This difference may reflect demographic asymmetries, since African and Asian populations experienced main expansions in middle Holocene, while in Europeans the main expansions occurred earlier in the post-glacial period.
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spelling Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potentialAfrican Continental Ancestry Group/geneticsAsian Continental Ancestry Group/geneticsCell Nucleus/geneticsDNA/geneticsDNA/metabolismDNA Mitochondrial/geneticsDNA Mitochondrial/metabolismDatabases GeneticEuropean Continental Ancestry Group/geneticsGenetic VariationHumansHydrophobic and Hydrophilic InteractionsMitochondrial Proteins/chemistryMitochondrial Proteins/immunologyMitochondrial Proteins/metabolismPolymorphism GeneticMitochondrial proteins are coded by nuclear (nDNA) and mitochondrial (mtDNA) genes, implying a complex cross-talk between the two genomes. Here we investigated the diversity displayed in 104 nuclear-coded mitochondrial proteins from 1,092 individuals from the 1000 Genomes dataset, in order to evaluate if these genes are under the effects of purifying selection and how that selection compares with their mitochondrial encoded counterparts. Only the very rare variants (frequency < 0.1%) in these nDNA genes are indistinguishable from a random set from all possible variants in terms of predicted pathogenicity score, but more frequent variants display distinct signs of purifying selection. Comparisons of selection strength indicate stronger selection in the mtDNA genes compared to this set of nDNA genes, accounted for by the high hydrophobicity of the proteins coded by the mtDNA. Most of the predicted pathogenic variants in the nDNA genes were restricted to a single continental population. The proportion of individuals having at least one potential pathogenic mutation in this gene set was significantly lower in Europeans than in Africans and Asians. This difference may reflect demographic asymmetries, since African and Asian populations experienced main expansions in middle Holocene, while in Europeans the main expansions occurred earlier in the post-glacial period.Nature Publishing Group20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfhttp://hdl.handle.net/10216/109251eng2045-232210.1038/srep07155Pereira, LSoares, PTriska, PRito, TWaerden, AvdLi, BRadivojac, PSamuels, DCinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T12:27:59Zoai:repositorio-aberto.up.pt:10216/109251Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:20:48.671222Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
title Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
spellingShingle Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
Pereira, L
African Continental Ancestry Group/genetics
Asian Continental Ancestry Group/genetics
Cell Nucleus/genetics
DNA/genetics
DNA/metabolism
DNA Mitochondrial/genetics
DNA Mitochondrial/metabolism
Databases Genetic
European Continental Ancestry Group/genetics
Genetic Variation
Humans
Hydrophobic and Hydrophilic Interactions
Mitochondrial Proteins/chemistry
Mitochondrial Proteins/immunology
Mitochondrial Proteins/metabolism
Polymorphism Genetic
title_short Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
title_full Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
title_fullStr Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
title_full_unstemmed Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
title_sort Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
author Pereira, L
author_facet Pereira, L
Soares, P
Triska, P
Rito, T
Waerden, Avd
Li, B
Radivojac, P
Samuels, DC
author_role author
author2 Soares, P
Triska, P
Rito, T
Waerden, Avd
Li, B
Radivojac, P
Samuels, DC
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pereira, L
Soares, P
Triska, P
Rito, T
Waerden, Avd
Li, B
Radivojac, P
Samuels, DC
dc.subject.por.fl_str_mv African Continental Ancestry Group/genetics
Asian Continental Ancestry Group/genetics
Cell Nucleus/genetics
DNA/genetics
DNA/metabolism
DNA Mitochondrial/genetics
DNA Mitochondrial/metabolism
Databases Genetic
European Continental Ancestry Group/genetics
Genetic Variation
Humans
Hydrophobic and Hydrophilic Interactions
Mitochondrial Proteins/chemistry
Mitochondrial Proteins/immunology
Mitochondrial Proteins/metabolism
Polymorphism Genetic
topic African Continental Ancestry Group/genetics
Asian Continental Ancestry Group/genetics
Cell Nucleus/genetics
DNA/genetics
DNA/metabolism
DNA Mitochondrial/genetics
DNA Mitochondrial/metabolism
Databases Genetic
European Continental Ancestry Group/genetics
Genetic Variation
Humans
Hydrophobic and Hydrophilic Interactions
Mitochondrial Proteins/chemistry
Mitochondrial Proteins/immunology
Mitochondrial Proteins/metabolism
Polymorphism Genetic
description Mitochondrial proteins are coded by nuclear (nDNA) and mitochondrial (mtDNA) genes, implying a complex cross-talk between the two genomes. Here we investigated the diversity displayed in 104 nuclear-coded mitochondrial proteins from 1,092 individuals from the 1000 Genomes dataset, in order to evaluate if these genes are under the effects of purifying selection and how that selection compares with their mitochondrial encoded counterparts. Only the very rare variants (frequency < 0.1%) in these nDNA genes are indistinguishable from a random set from all possible variants in terms of predicted pathogenicity score, but more frequent variants display distinct signs of purifying selection. Comparisons of selection strength indicate stronger selection in the mtDNA genes compared to this set of nDNA genes, accounted for by the high hydrophobicity of the proteins coded by the mtDNA. Most of the predicted pathogenic variants in the nDNA genes were restricted to a single continental population. The proportion of individuals having at least one potential pathogenic mutation in this gene set was significantly lower in Europeans than in Africans and Asians. This difference may reflect demographic asymmetries, since African and Asian populations experienced main expansions in middle Holocene, while in Europeans the main expansions occurred earlier in the post-glacial period.
publishDate 2014
dc.date.none.fl_str_mv 2014
2014-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10216/109251
url http://hdl.handle.net/10216/109251
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2045-2322
10.1038/srep07155
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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