Multiple loss-of-function variants of taste receptors in modern humans

被引:0
|
作者
Kohei Fujikura
机构
[1] Kobe University School of Medicine,
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Despite recent advances in the knowledge of interindividual taste differences, the underlying genetic backgrounds have remained to be fully elucidated. Much of the taste variation among different mammalian species can be explained by pseudogenization of taste receptors. Here I investigated whether the most recent disruptions of taste receptor genes segregate with their intact forms in modern humans by analyzing 14 ethnically diverse populations. The results revealed an unprecedented prevalence of 25 segregating loss-of-function (LoF) taste receptor variants, identifying one of the most pronounced cases of functional population diversity in the human genome. LoF variant frequency in taste receptors (2.10%) was considerably higher than the overall LoF frequency in human genome (0.16%). In particular, molecular evolutionary rates of candidate sour (14.7%) and bitter (1.8%) receptors were far higher in humans than those of sweet (0.02%), salty (0.05%) and umami (0.17%) receptors compared with other carnivorous mammals, although not all of the taste receptors were identified. Many LoF variants are population-specific, some of which arose even after population differentiation, not before divergence of the modern and archaic human. I conclude that modern humans might have been losing some sour and bitter receptor genes because of high-frequency LoF variants.
引用
收藏
相关论文
共 50 条
  • [1] Multiple loss-of-function variants of taste receptors in modern humans
    Fujikura, K.
    SCIENTIFIC REPORTS, 2015, 5
  • [2] Correction: Corrigendum: Multiple loss-of-function variants of taste receptors in modern humans
    Kohei Fujikura
    Scientific Reports, 6
  • [3] Multiple loss-of-function variants of taste receptors in modern humans (vol 5, 12349, 2015)
    Fujikura, Kohei
    SCIENTIFIC REPORTS, 2016, 6
  • [4] Loss-of-function variants in the genomes of healthy humans
    MacArthur, Daniel G.
    Tyler-Smith, Chris
    HUMAN MOLECULAR GENETICS, 2010, 19 : R125 - R130
  • [5] Loss-of-function variants
    Orli Bahcall
    Nature Genetics, 2012, 44 (4) : 368 - 368
  • [6] The effect of LRRK2 loss-of-function variants in humans
    Nicola Whiffin
    Irina M. Armean
    Aaron Kleinman
    Jamie L. Marshall
    Eric V. Minikel
    Julia K. Goodrich
    Nicholas M. Quaife
    Joanne B. Cole
    Qingbo Wang
    Konrad J. Karczewski
    Beryl B. Cummings
    Laurent Francioli
    Kristen Laricchia
    Anna Guan
    Babak Alipanahi
    Peter Morrison
    Marco A. S. Baptista
    Kalpana M. Merchant
    James S. Ware
    Aki S. Havulinna
    Bozenna Iliadou
    Jung-Jin Lee
    Girish N. Nadkarni
    Cole Whiteman
    Mark Daly
    Tõnu Esko
    Christina Hultman
    Ruth J. F. Loos
    Lili Milani
    Aarno Palotie
    Carlos Pato
    Michele Pato
    Danish Saleheen
    Patrick F. Sullivan
    Jessica Alföldi
    Paul Cannon
    Daniel G. MacArthur
    Nature Medicine, 2020, 26 : 869 - 877
  • [7] The effect of LRRK2 loss-of-function variants in humans
    Whiffin, Nicola
    Armean, Irina M.
    Kleinman, Aaron
    Marshall, Jamie L.
    Minikel, Eric V.
    Goodrich, Julia K.
    Quaife, Nicholas M.
    Cole, Joanne B.
    Wang, Qingbo
    Karczewski, Konrad J.
    Cummings, Beryl B.
    Francioli, Laurent
    Laricchia, Kristen
    Guan, Anna
    Alipanahi, Babak
    Morrison, Peter
    Baptista, Marco A. S.
    Merchant, Kalpana M.
    Ware, James S.
    Havulinna, Aki S.
    Iliadou, Bozenna
    Lee, Jung-Jin
    Nadkarni, Girish N.
    Whiteman, Cole
    Daly, Mark
    Esko, Tonu
    Hultman, Christina
    Loos, Ruth J. F.
    Milani, Lili
    Palotie, Aarno
    Pato, Carlos
    Pato, Michele
    Saleheen, Danish
    Sullivan, Patrick F.
    Alfoldi, Jessica
    Cannon, Paul
    MacArthur, Daniel G.
    NATURE MEDICINE, 2020, 26 (06) : 869 - +
  • [8] Loss-of-function variants in myocardin cause congenital megabladder in humans and mice
    Houweling, Arjan C.
    Beaman, Glenda M.
    Postma, Alex V.
    Gainous, T. Blair
    Lichtenbelt, Klaske D.
    Brancati, Francesco
    Lopes, Filipa M.
    van der Made, Ingeborg
    Polstra, Abeltje M.
    Robinson, Michael L.
    Wright, Kevin D.
    Ellingford, Jamie M.
    Jackson, Ashley R.
    Overwater, Eline
    Genesio, Rita
    Romano, Silvio
    Camerota, Letizia
    D'Angelo, Emanuela
    Meijers-Heijboer, Elizabeth J.
    Christoffels, Vincent M.
    McHugh, Kirk M.
    Black, Brian L.
    Newman, William G.
    Woolf, Adrian S.
    Creemers, Esther E.
    JOURNAL OF CLINICAL INVESTIGATION, 2019, 129 (12): : 5374 - 5380
  • [9] Loss-of-function variants in myocardin cause congenital megabladder in humans and mice
    Houweling, A.
    Beaman, G.
    Postma, A.
    Gainous, B.
    Lichtenbelt, K.
    Brancati, F.
    Lopes, F.
    van der Made, I.
    Polstra, A.
    Robinson, M.
    Wright, K.
    Jackson, A.
    Genesio, R.
    Camerota, L.
    D'Angelo, E.
    Meijers-Heijboer, E.
    Christoffels, V.
    McHugh, K.
    Black, B.
    Newman, W.
    Woolf, A.
    Creemers, E.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1144 - 1145
  • [10] Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans
    Edmondson, Andrew C.
    Brown, Robert J.
    Kathiresan, Sekar
    Cupples, L. Adrienne
    Demissie, Serkalem
    Manning, Alisa Knodle
    Jensen, Majken K.
    Rimm, Eric B.
    Wang, Jian
    Rodrigues, Amrith
    Bamba, Vaneeta
    Khetarpal, Sumeet A.
    Wolfe, Megan L.
    DerOhannessian, Stephanie
    Li, Mingyao
    Reilly, Muredach P.
    Aberle, Jens
    Evans, David
    Hegele, Robert A.
    Rader, Daniel J.
    JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (04): : 1042 - 1050