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Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection.
Zhang, Chao; Verma, Anurag; Feng, Yuanqing; Melo, Marcelo C R; McQuillan, Michael; Hansen, Matthew; Lucas, Anastasia; Park, Joseph; Ranciaro, Alessia; Thompson, Simon; Rubel, Meagan A; Campbell, Michael C; Beggs, William; Hirbo, Jibril; Wata Mpoloka, Sununguko; George Mokone, Gaonyadiwe; Nyambo, Thomas; Wolde Meskel, Dawit; Belay, Gurja; Fokunang, Charles; Njamnshi, Alfred K; Omar, Sabah A; Williams, Scott M; Rader, Daniel J; Ritchie, Marylyn D; de la Fuente-Nunez, Cesar; Sirugo, Giorgio; Tishkoff, Sarah A.
Afiliação
  • Zhang C; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Verma A; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Feng Y; Division of Translational Medicine and Human Genetics, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104.
  • Melo MCR; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • McQuillan M; Machine Biology Group, Departments of Psychiatry and Microbiology, Institute for Biomedical Informatics, Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Hansen M; Departments of Bioengineering and Chemical and Biomolecular Engineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA 19104.
  • Lucas A; Penn Institute for Computational Science, University of Pennsylvania, Philadelphia, PA 19104.
  • Park J; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Ranciaro A; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Thompson S; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Rubel MA; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Campbell MC; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Beggs W; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Hirbo J; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Wata Mpoloka S; Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089.
  • George Mokone G; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • Nyambo T; Biological Sciences, University of Botswana, Gaborone, Botswana.
  • Wolde Meskel D; Faculty of Medicine, University of Botswana, Gaborone, Botswana.
  • Belay G; Regeneron Genetics Center, Tarrytown, NY 10591.
  • Fokunang C; Department of Biochemistry, Kampala International University in Tanzania, Dar es Salaam, Tanzania.
  • Njamnshi AK; Department of Microbial Cellular and Molecular Biology, Addis Ababa University, Addis Ababa, Ethiopia.
  • Omar SA; Department of Microbial Cellular and Molecular Biology, Addis Ababa University, Addis Ababa, Ethiopia.
  • Williams SM; Department of Pharmacotoxicology and Pharmacokinetics, Faculty of Medicine and Biomedical Sciences, The University of Yaoundé I, Yaoundé, Cameroon.
  • Rader DJ; Department of Neurology, Central Hospital Yaoundé, Yaoundé, Cameroon.
  • Ritchie MD; Brain Research Africa Initiative, Neuroscience Laboratory, Faculty of Medicine and Biomedical Sciences, The University of Yaoundé I, Yaoundé, Cameroon.
  • de la Fuente-Nunez C; Center for Biotechnology Research and Development, Kenya Medical Research Institute, Nairobi, Kenya.
  • Sirugo G; Department of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH 44106.
  • Tishkoff SA; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Proc Natl Acad Sci U S A ; 119(21): e2123000119, 2022 05 24.
Article em En | MEDLINE | ID: mdl-35580180
ABSTRACT
Human genomic diversity has been shaped by both ancient and ongoing challenges from viruses. The current coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has had a devastating impact on population health. However, genetic diversity and evolutionary forces impacting host genes related to SARS-CoV-2 infection are not well understood. We investigated global patterns of genetic variation and signatures of natural selection at host genes relevant to SARS-CoV-2 infection (angiotensin converting enzyme 2 [ACE2], transmembrane protease serine 2 [TMPRSS2], dipeptidyl peptidase 4 [DPP4], and lymphocyte antigen 6 complex locus E [LY6E]). We analyzed data from 2,012 ethnically diverse Africans and 15,977 individuals of European and African ancestry with electronic health records and integrated with global data from the 1000 Genomes Project. At ACE2, we identified 41 nonsynonymous variants that were rare in most populations, several of which impact protein function. However, three nonsynonymous variants (rs138390800, rs147311723, and rs145437639) were common among central African hunter-gatherers from Cameroon (minor allele frequency 0.083 to 0.164) and are on haplotypes that exhibit signatures of positive selection. We identify signatures of selection impacting variation at regulatory regions influencing ACE2 expression in multiple African populations. At TMPRSS2, we identified 13 amino acid changes that are adaptive and specific to the human lineage compared with the chimpanzee genome. Genetic variants that are targets of natural selection are associated with clinical phenotypes common in patients with COVID-19. Our study provides insights into global variation at host genes related to SARS-CoV-2 infection, which have been shaped by natural selection in some populations, possibly due to prior viral infections.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Tipo de estudo: Risk_factors_studies Limite: Humans País/Região como assunto: Africa Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Tipo de estudo: Risk_factors_studies Limite: Humans País/Região como assunto: Africa Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2022 Tipo de documento: Article