TY - JOUR
T1 - Epigenetic and genetic components of height regulation
AU - Benonisdottir, Stefania
AU - Oddsson, Asmundur
AU - Helgason, Agnar
AU - Kristjansson, Ragnar P.
AU - Sveinbjornsson, Gardar
AU - Oskarsdottir, Arna
AU - Thorleifsson, Gudmar
AU - Davidsson, Olafur B.
AU - Arnadottir, Gudny A.
AU - Sulem, Gerald
AU - Jensson, Brynjar O.
AU - Holm, Hilma
AU - Alexandersson, Kristjan F.
AU - Tryggvadottir, Laufey
AU - Walters, G. Bragi
AU - Gudjonsson, Sigurjon A.
AU - Ward, Lucas D.
AU - Sigurdsson, Jon K.
AU - Iordache, Paul D.
AU - Frigge, Michael L.
AU - Rafnar, Thorunn
AU - Kong, Augustine
AU - Masson, Gisli
AU - Helgason, Hannes
AU - Thorsteinsdottir, Unnur
AU - Gudbjartsson, Daniel F.
AU - Sulem, Patrick
AU - Stefansson, Kari
N1 - Publisher Copyright: © The Author(s) 2016.
PY - 2016/11/16
Y1 - 2016/11/16
N2 - Adult height is a highly heritable trait. Here we identified 31.6 million sequence variants by whole-genome sequencing of 8,453 Icelanders and tested them for association with adult height by imputing them into 88,835 Icelanders. Here we discovered 13 novel height associations by testing four different models including parent-of-origin (|β|=0.4-10.6 cm). The minor alleles of three parent-of-origin signals associate with less height only when inherited from the father and are located within imprinted regions (IGF2-H19 and DLK1-MEG3). We also examined the association of these sequence variants in a set of 12,645 Icelanders with birth length measurements. Two of the novel variants, (IGF2-H19 and TET1), show significant association with both adult height and birth length, indicating a role in early growth regulation. Among the parent-of-origin signals, we observed opposing parental effects raising questions about underlying mechanisms. These findings demonstrate that common variations affect human growth by parental imprinting.
AB - Adult height is a highly heritable trait. Here we identified 31.6 million sequence variants by whole-genome sequencing of 8,453 Icelanders and tested them for association with adult height by imputing them into 88,835 Icelanders. Here we discovered 13 novel height associations by testing four different models including parent-of-origin (|β|=0.4-10.6 cm). The minor alleles of three parent-of-origin signals associate with less height only when inherited from the father and are located within imprinted regions (IGF2-H19 and DLK1-MEG3). We also examined the association of these sequence variants in a set of 12,645 Icelanders with birth length measurements. Two of the novel variants, (IGF2-H19 and TET1), show significant association with both adult height and birth length, indicating a role in early growth regulation. Among the parent-of-origin signals, we observed opposing parental effects raising questions about underlying mechanisms. These findings demonstrate that common variations affect human growth by parental imprinting.
UR - https://www.scopus.com/pages/publications/84995475478
U2 - 10.1038/ncomms13490
DO - 10.1038/ncomms13490
M3 - Article
C2 - 27848971
SN - 2041-1723
VL - 7
JO - Nature Communications
JF - Nature Communications
M1 - 13490
ER -