Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.

Hans Eiberg; Jesper Troelsen; Mette Boyd; Annemette Friis Mikkelsen; Jonas Mengel-From; Klaus W Kjaer; Lars Hansen

doi:10.1007/s00439-007-0460-x

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.

Hans Eiberg, Jesper Troelsen, Mette Boyd, Annemette Friis Mikkelsen, Jonas Mengel-From, Klaus W Kjaer, Lars Hansen

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

268 Citationer (Scopus)

Abstract

Udgivelsesdato: 2008-Mar

Originalsprog	Engelsk
Tidsskrift	Human Genetics
Vol/bind	123
Udgave nummer	2
Sider (fra-til)	177-87
Antal sider	10
ISSN	0340-6717
DOI	https://doi.org/10.1007/s00439-007-0460-x
Status	Udgivet - 2008

Bibliografisk note

Keywords: Adult; Alleles; Cells, Cultured; Chromosomes, Human, Pair 15; Denmark; Eye Color; Female; Founder Effect; Gene Expression Regulation; Genotype; Guanine Nucleotide Exchange Factors; Hair Color; Haplotypes; Humans; Linkage (Genetics); Lod Score; Luciferases; Male; Membrane Transport Proteins; Mutation; Pedigree; Polymorphism, Single Nucleotide; Questionnaires; Regulatory Sequences, Nucleic Acid

Adgang til dokumentet

10.1007/s00439-007-0460-x

Citationsformater

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression. / Eiberg, Hans; Troelsen, Jesper; Boyd, Mette; Mikkelsen, Annemette Friis; Mengel-From, Jonas; Kjaer, Klaus W; Hansen, Lars.

I: Human Genetics, Bind 123, Nr. 2, 2008, s. 177-87.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

@article{2afe72c078e711dd81b0000ea68e967b,

title = "Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.",

abstract = "The human eye color is a quantitative trait displaying multifactorial inheritance. Several studies have shown that the OCA2 locus is the major contributor to the human eye color variation. By linkage analysis of a large Danish family, we finemapped the blue eye color locus to a 166 Kbp region within the HERC2 gene. By association analyses, we identified two SNPs within this region that were perfectly associated with the blue and brown eye colors: rs12913832 and rs1129038. Of these, rs12913832 is located 21.152 bp upstream from the OCA2 promoter in a highly conserved sequence in intron 86 of HERC2. The brown eye color allele of rs12913832 is highly conserved throughout a number of species. As shown by a Luciferase assays in cell cultures, the element significantly reduces the activity of the OCA2 promoter and electrophoretic mobility shift assays demonstrate that the two alleles bind different subsets of nuclear extracts. One single haplotype, represented by six polymorphic SNPs covering half of the 3' end of the HERC2 gene, was found in 155 blue-eyed individuals from Denmark, and in 5 and 2 blue-eyed individuals from Turkey and Jordan, respectively. Hence, our data suggest a common founder mutation in an OCA2 inhibiting regulatory element as the cause of blue eye color in humans. In addition, an LOD score of Z = 4.21 between hair color and D14S72 was obtained in the large family, indicating that RABGGTA is a candidate gene for hair color.",

author = "Hans Eiberg and Jesper Troelsen and Mette Boyd and Mikkelsen, {Annemette Friis} and Jonas Mengel-From and Kjaer, {Klaus W} and Lars Hansen",

note = "Keywords: Adult; Alleles; Cells, Cultured; Chromosomes, Human, Pair 15; Denmark; Eye Color; Female; Founder Effect; Gene Expression Regulation; Genotype; Guanine Nucleotide Exchange Factors; Hair Color; Haplotypes; Humans; Linkage (Genetics); Lod Score; Luciferases; Male; Membrane Transport Proteins; Mutation; Pedigree; Polymorphism, Single Nucleotide; Questionnaires; Regulatory Sequences, Nucleic Acid",

year = "2008",

doi = "10.1007/s00439-007-0460-x",

language = "English",

volume = "123",

pages = "177--87",

journal = "Human Genetics",

issn = "0340-6717",

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T1 - Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.

AU - Eiberg, Hans

AU - Troelsen, Jesper

AU - Boyd, Mette

AU - Mikkelsen, Annemette Friis

AU - Mengel-From, Jonas

AU - Kjaer, Klaus W

AU - Hansen, Lars

N1 - Keywords: Adult; Alleles; Cells, Cultured; Chromosomes, Human, Pair 15; Denmark; Eye Color; Female; Founder Effect; Gene Expression Regulation; Genotype; Guanine Nucleotide Exchange Factors; Hair Color; Haplotypes; Humans; Linkage (Genetics); Lod Score; Luciferases; Male; Membrane Transport Proteins; Mutation; Pedigree; Polymorphism, Single Nucleotide; Questionnaires; Regulatory Sequences, Nucleic Acid

PY - 2008

Y1 - 2008

N2 - The human eye color is a quantitative trait displaying multifactorial inheritance. Several studies have shown that the OCA2 locus is the major contributor to the human eye color variation. By linkage analysis of a large Danish family, we finemapped the blue eye color locus to a 166 Kbp region within the HERC2 gene. By association analyses, we identified two SNPs within this region that were perfectly associated with the blue and brown eye colors: rs12913832 and rs1129038. Of these, rs12913832 is located 21.152 bp upstream from the OCA2 promoter in a highly conserved sequence in intron 86 of HERC2. The brown eye color allele of rs12913832 is highly conserved throughout a number of species. As shown by a Luciferase assays in cell cultures, the element significantly reduces the activity of the OCA2 promoter and electrophoretic mobility shift assays demonstrate that the two alleles bind different subsets of nuclear extracts. One single haplotype, represented by six polymorphic SNPs covering half of the 3' end of the HERC2 gene, was found in 155 blue-eyed individuals from Denmark, and in 5 and 2 blue-eyed individuals from Turkey and Jordan, respectively. Hence, our data suggest a common founder mutation in an OCA2 inhibiting regulatory element as the cause of blue eye color in humans. In addition, an LOD score of Z = 4.21 between hair color and D14S72 was obtained in the large family, indicating that RABGGTA is a candidate gene for hair color.

AB - The human eye color is a quantitative trait displaying multifactorial inheritance. Several studies have shown that the OCA2 locus is the major contributor to the human eye color variation. By linkage analysis of a large Danish family, we finemapped the blue eye color locus to a 166 Kbp region within the HERC2 gene. By association analyses, we identified two SNPs within this region that were perfectly associated with the blue and brown eye colors: rs12913832 and rs1129038. Of these, rs12913832 is located 21.152 bp upstream from the OCA2 promoter in a highly conserved sequence in intron 86 of HERC2. The brown eye color allele of rs12913832 is highly conserved throughout a number of species. As shown by a Luciferase assays in cell cultures, the element significantly reduces the activity of the OCA2 promoter and electrophoretic mobility shift assays demonstrate that the two alleles bind different subsets of nuclear extracts. One single haplotype, represented by six polymorphic SNPs covering half of the 3' end of the HERC2 gene, was found in 155 blue-eyed individuals from Denmark, and in 5 and 2 blue-eyed individuals from Turkey and Jordan, respectively. Hence, our data suggest a common founder mutation in an OCA2 inhibiting regulatory element as the cause of blue eye color in humans. In addition, an LOD score of Z = 4.21 between hair color and D14S72 was obtained in the large family, indicating that RABGGTA is a candidate gene for hair color.

U2 - 10.1007/s00439-007-0460-x

DO - 10.1007/s00439-007-0460-x

M3 - Journal article

C2 - 18172690

VL - 123

SP - 177

EP - 187

JO - Human Genetics

JF - Human Genetics

SN - 0340-6717

IS - 2

ER -