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Integrative functional genomic analyses identify genetic variants influencing skin pigmentation in Africans.
Feng, Yuanqing; Xie, Ning; Inoue, Fumitaka; Fan, Shaohua; Saskin, Joshua; Zhang, Chao; Zhang, Fang; Hansen, Matthew E B; Nyambo, Thomas; Mpoloka, Sununguko Wata; Mokone, Gaonyadiwe George; Fokunang, Charles; Belay, Gurja; Njamnshi, Alfred K; Marks, Michael S; Oancea, Elena; Ahituv, Nadav; Tishkoff, Sarah A.
Afiliação
  • Feng Y; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
  • Xie N; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
  • Inoue F; Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA, USA.
  • Fan S; Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Saskin J; Institute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto, Japan.
  • Zhang C; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
  • Zhang F; Human Phenome Institute, School of Life Science, Fudan University, Shanghai, China.
  • Hansen MEB; Department of Neuroscience, Brown University, Providence, RI, USA.
  • Nyambo T; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
  • Mpoloka SW; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
  • Mokone GG; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
  • Fokunang C; Department of Biochemistry and Molecular Biology, Hubert Kairuki Memorial University, Dar es Salaam, Tanzania.
  • Belay G; Department of Biological Sciences, Faculty of Sciences, University of Botswana, Gaborone, Botswana.
  • Njamnshi AK; Department of Biomedical Sciences, University of Botswana, Gaborone, Botswana.
  • Marks MS; Department of Pharmacotoxicology and Pharmacokinetics, Faculty of Medicine and Biomedical Sciences, The University of Yaoundé I, Yaoundé, Cameroon.
  • Oancea E; Department of Biology, Addis Ababa University, Addis Ababa, Ethiopia.
  • Ahituv N; Brain Research Africa Initiative (BRAIN); Neuroscience Lab, Faculty of Medicine and Biomedical Sciences, The University of Yaoundé I, Department of Neurology, Central Hospital Yaoundé, Yaoundé, Cameroon.
  • Tishkoff SA; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia Research Institute, Philadelphia, PA, USA.
Nat Genet ; 56(2): 258-272, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38200130
ABSTRACT
Skin color is highly variable in Africans, yet little is known about the underlying molecular mechanism. Here we applied massively parallel reporter assays to screen 1,157 candidate variants influencing skin pigmentation in Africans and identified 165 single-nucleotide polymorphisms showing differential regulatory activities between alleles. We combine Hi-C, genome editing and melanin assays to identify regulatory elements for MFSD12, HMG20B, OCA2, MITF, LEF1, TRPS1, BLOC1S6 and CYB561A3 that impact melanin levels in vitro and modulate human skin color. We found that independent mutations in an OCA2 enhancer contribute to the evolution of human skin color diversity and detect signals of local adaptation at enhancers of MITF, LEF1 and TRPS1, which may contribute to the light skin color of Khoesan-speaking populations from Southern Africa. Additionally, we identified CYB561A3 as a novel pigmentation regulator that impacts genes involved in oxidative phosphorylation and melanogenesis. These results provide insights into the mechanisms underlying human skin color diversity and adaptive evolution.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Pigmentação da Pele / Albinismo Oculocutâneo / Melaninas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Pigmentação da Pele / Albinismo Oculocutâneo / Melaninas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos