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Association of the Polymorphism His615Arg with Melanin Content in East Asian Populations: Further Evidence of Convergent Evolution of Skin Pigmentation


The last decade has witnessed important advances in our understanding of the genetics of pigmentation in European populations, but very little is known about the genes involved in skin pigmentation variation in East Asian populations. Here, we present the results of a study evaluating the association of 10 Single Nucleotide Polymorphisms (SNPs) located within 5 pigmentation candidate genes (OCA2, DCT, ADAM17, ADAMTS20, and TYRP1) with skin pigmentation measured quantitatively in a sample of individuals of East Asian ancestry living in Canada. We show that the non-synonymous polymorphism rs1800414 (His615Arg) located within the OCA2 gene is significantly associated with skin pigmentation in this sample. We replicated this result in an independent sample of Chinese individuals of Han ancestry. This polymorphism is characterized by a derived allele that is present at a high frequency in East Asian populations, but is absent in other population groups. In both samples, individuals with the derived G allele, which codes for the amino acid arginine, show lower melanin levels than those with the ancestral A allele, which codes for the amino acid histidine. An analysis of this non-synonymous polymorphism using several programs to predict potential functional effects provides additional support for the role of this SNP in skin pigmentation variation in East Asian populations. Our results are consistent with previous research indicating that evolution to lightly-pigmented skin occurred, at least in part, independently in Europe and East Asia.


Vyšlo v časopise: Association of the Polymorphism His615Arg with Melanin Content in East Asian Populations: Further Evidence of Convergent Evolution of Skin Pigmentation. PLoS Genet 6(3): e32767. doi:10.1371/journal.pgen.1000867
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1000867

Souhrn

The last decade has witnessed important advances in our understanding of the genetics of pigmentation in European populations, but very little is known about the genes involved in skin pigmentation variation in East Asian populations. Here, we present the results of a study evaluating the association of 10 Single Nucleotide Polymorphisms (SNPs) located within 5 pigmentation candidate genes (OCA2, DCT, ADAM17, ADAMTS20, and TYRP1) with skin pigmentation measured quantitatively in a sample of individuals of East Asian ancestry living in Canada. We show that the non-synonymous polymorphism rs1800414 (His615Arg) located within the OCA2 gene is significantly associated with skin pigmentation in this sample. We replicated this result in an independent sample of Chinese individuals of Han ancestry. This polymorphism is characterized by a derived allele that is present at a high frequency in East Asian populations, but is absent in other population groups. In both samples, individuals with the derived G allele, which codes for the amino acid arginine, show lower melanin levels than those with the ancestral A allele, which codes for the amino acid histidine. An analysis of this non-synonymous polymorphism using several programs to predict potential functional effects provides additional support for the role of this SNP in skin pigmentation variation in East Asian populations. Our results are consistent with previous research indicating that evolution to lightly-pigmented skin occurred, at least in part, independently in Europe and East Asia.


Zdroje

1. ParraEJ

2007 Human pigmentation variation: evolution, genetic basis, and implications for public health. Am J Phys Anthropol Suppl 45 85 105

2. SturmRA

2009 Molecular genetics of human pigmentation diversity. Hum Mol Genet 18 R9 17

3. LamasonRL

MohideenMA

MestJR

WongAC

NortonHL

2005 SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310 1782 1786

4. GrafJ

HodgsonR

van DaalA

2005 Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation. Hum Mutation 25 278 284

5. NortonHL

KittlesRA

ParraE

McKeigueP

MaoX

2007 Genetic evidence for the convergent evolution of light skin in Europeans and East Asians. Mol Biol Evol 24 710 722

6. MillerCT

BelezaS

PollenAA

SchluterD

KittlesRA

2007 Cis-regulatory changes in Kit Ligand expression and parallel evolution of pigmentation in sticklebacks and humans. Cell 131 1179 1189

7. ShriverMD

ParraEJ

DiosS

BonillaC

NortonH

2003 Skin pigmentation, biogeographical ancestry and admixture mapping. Hum Genet 112 387 399

8. AkeyJM

WangH

XiongM

WuH

LiuW

2001 Interaction between the melanocortin-1 receptor and P genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population. Hum Genet 108 516 520

9. MakovaK

NortonH

2005 Worldwide polymorphism at the MC1R and normal pigmentation variation in humans. Peptides 26 1901 1908

10. KanetskyPA

SwoyerJ

PanossianS

HolmesR

GuerryD

2002 A polymorphism in the agouti signaling protein gene is associated with human pigmentation. Am J Hum Genet 70 770 775

11. BonillaC

BoxillLA

DonaldSA

WilliamsT

SylvesterN

2005 The 8818G allele of the agouti signaling protein (ASIP) gene is ancestral and is associated with darker skin color in African Americans. Hum Genet 116 402 406

12. VoiseyJ

Gomez-Cabrera M delC

SmitDJ

LeonardJH

SturmRA

2006 A polymorphism in the agouti signaling protein (ASIP) is associated with decreased levels of mRNA. Pigment Cell Res 19 226 231

13. HanJ

KraftP

NanH

GuoQ

ChenC

2008 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. PLoS Genet 4 e1000074 doi:10.1371/journal.pgen.1000074

14. StokowskiRP

PantPV

DaddT

FeredayA

HindsDA

2007 A genomewide association study of skin pigmentation in a South Asian populations. Am J Hum Genet 81 1119 1132

15. VoightBF

KudaravalliS

WenX

PritchardJK

2006 A map of recent positive selection in the human genome. PLoS Biol 4 e72 doi:10.1371/journal.pbio.0040072

16. McEvoyB

BelezaS

ShriverMD

2006 The genetic architecture of normal variation in human pigmentation: an evolutionary perspective and model. Hum Mol Genet 15 Spec No 2 R176 R181

17. IzagirreN

GarciaI

JunqueraC

de la RuaC

AlonsoS

2006 A scan for signatures of positive selection in candidate loci for skin pigmentation in humans. Mol Biol Evol 23 1697 1706

18. MylesS

SomelM

TangK

KelsoJ

StonekingM

2007 Identifying genes underlying pigmentation differences among human populations. Hum Genet 120 613 621

19. LaoO

de GruijterJM

van DuijnK

NavarroA

KayserM

2007 Signatures of positive selection in genes associated with human skin pigmentation as revealed from analyses of single nucleotide polymorphisms. Ann Hum Genet 71 354 369

20. AlonsoS

IzagirreN

Smith-ZubiagaI

GardeazabalJ

Diaz-RamonJL

2008 Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans. BMC Evol Biol 8 74

21. DonnellyMP

SpeedWC

KiddJR

PakstisAJ

KiddKK

2009 Selection for blue eyes in Europe and light skin pigmentation in East Asia at OCA2/HERC2. Platform Abstract #294. The American Society of Human Genetics 59th Annual meeting. Available at http://www.ashg.org/2009meeting/pdf/platforms_4up.pdf

22. KelleyJL

MadeoyJ

CalhounJC

SwansonW

AkeyJM

2006 Genomic signatures of positive selection in humans and the limits of outlier approaches. Genome Res 16 980 989

23. TeshimaKM

CoopG

PrzeworskiM

2006 How reliable are empirical genomic scans for selective sweeps? Genome Res 16 702 712

24. EibergH

TroelsenJ

NielsenM

MikkelsenA

Mengel-FromJ

2008 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. Hum Genet 123 177 187

25. SturmRA

DuffyDL

ZhaoZZ

LeiteFP

StarkMS

2008 A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color. Am J Hum Genet 82 424 431

26. KayserM

LiuF

JanssensAC

RivadeneiraF

LaoO

2008 Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene. Am J Hum Genet 82 411 423

27. CookAL

ChenW

ThurberAE

SmitDJ

SmithAG

2009 Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P loci. J Invest Dermatol 129 392 405

28. YuasaI

UmetsuK

HariharaS

KidoA

MiyoshiA

2007 Distribution of two Asian-related coding SNPs in the MC1R and OCA2 genes. Biochem Genet 45 535 542

29. AnnoS

AbeT

YamamotoT

2008 Interactions between SNP alleles at multiple loci contribute to skin color differences between Caucasoid and Mongoloid subjects. Int J Biol Sci 4 81 86

30. LeeST

NichollsRD

JongMT

FukaiK

SpritzRA

1995 Organization and sequence of the human P gene and identification of a new family of transport proteins. Genomics 26 354 363

31. SviderskayaEV

BennettDC

HoL

BailinT

LeeST

SpritzRA

1997 Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences. J Invest Dermatol 108 30 34

32. GibbonsA

2007 American Association of Physical Anthropologists meeting. European skin turned pale only recently, gene suggests. Science 316 364

33. ShriverMD

ParraEJ

2000 Comparison of narrow-band reflectance spectroscopy and tristimulus colorimetry for measurements of skin and hair color in persons of different biological ancestry. Am J Phys Anthropol 112 17 27

34. JablonskiNG

ChaplinG

2000 The evolution of human skin coloration. J Hum Evol 39 57 106

35. RohK

KimD

HaS

RoY

KimJ

LeeH

2001 Pigmentation in Koreans: study of the differences from caucasians in age, gender and seasonal variations. Br J Dermatol 144 94 99

36. TajimaF

1989 Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123 585 595

37. ZhangC

BaileyDK

AwadT

LiuG

XingG

2006 A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations. Bioinformatics 22 2122 2128

38. ShriverM

KennedyGC

ParraEJ

LawsonHA

HuangJ

2004 The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs. Human Genomics 1 274 286

39. StorzJF

PayseurBA

NachmanMW

2004 Genome scans of DNA variability in humans reveal evidence for selective sweeps outside of Africa. Mol Biol Evol 21 1800 1811

40. BighamA

MaoX

BrutsaertT

WilsonM

JulianCG

2009 Identifying positive selection candidate loci for high-altitude adaptation in Andean populations. Human Genomics 4 79 90

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