Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.legalmed.2016.12.013 http://hdl.handle.net/11449/176974 |
Resumo: | The Solute Carrier Family 45, Member 2 (SLC45A2) gene encodes the Membrane-Associated Transporter Protein (MATP), which mediates melanin synthesis by tyrosinase trafficking and proton transportation to melanosomes. At least two SLC45A2 coding SNPs [E272K (rs26722) and L374F (rs16891982)] were reported influencing normal variation of human pigmentation. Here we aimed at evaluating the influence of haplotypes of 12 SNPs within SLC45A2 in the determination of eye, hair and skin pigmentation in a highly admixed population sample and comparing their frequencies with the ones found in data retrieved from the 1000 Genomes Project. To achieve this goal, 12 SLC45A2 SNPs were evaluated in 288 unrelated individuals from the Ribeirão Preto city area, Southeastern Brazil. SNPs were genotyped by PCR-RFLP or Allele-specific PCR, followed by polyacrylamide gel electrophoresis. Haplotypes of each individual were inferred by two independent computational methods, PHASE and Partition-Ligation–Expectation-Maximization (PL-EM) algorithms, and 34 different haplotypes were identified. The hp9 haplotype was the most frequent (58.3%) and was associated with the presence of blond/red hair, pale skin, blue eyes and freckles. All haplotypes significantly associated with dark or light pigmentation features harbor the 374L and 374F alleles, respectively. These results emphasize the role played by haplotypes at SLC45A2 in the determination of pigmentation aspects of human populations and reinforce the relevance of SNP L374F in human pigmentation. |
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Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in BrazilBrazilHaplotypesPigmentationSLC45A2SNPsThe Solute Carrier Family 45, Member 2 (SLC45A2) gene encodes the Membrane-Associated Transporter Protein (MATP), which mediates melanin synthesis by tyrosinase trafficking and proton transportation to melanosomes. At least two SLC45A2 coding SNPs [E272K (rs26722) and L374F (rs16891982)] were reported influencing normal variation of human pigmentation. Here we aimed at evaluating the influence of haplotypes of 12 SNPs within SLC45A2 in the determination of eye, hair and skin pigmentation in a highly admixed population sample and comparing their frequencies with the ones found in data retrieved from the 1000 Genomes Project. To achieve this goal, 12 SLC45A2 SNPs were evaluated in 288 unrelated individuals from the Ribeirão Preto city area, Southeastern Brazil. SNPs were genotyped by PCR-RFLP or Allele-specific PCR, followed by polyacrylamide gel electrophoresis. Haplotypes of each individual were inferred by two independent computational methods, PHASE and Partition-Ligation–Expectation-Maximization (PL-EM) algorithms, and 34 different haplotypes were identified. The hp9 haplotype was the most frequent (58.3%) and was associated with the presence of blond/red hair, pale skin, blue eyes and freckles. All haplotypes significantly associated with dark or light pigmentation features harbor the 374L and 374F alleles, respectively. These results emphasize the role played by haplotypes at SLC45A2 in the determination of pigmentation aspects of human populations and reinforce the relevance of SNP L374F in human pigmentation.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Departamento de Genética Faculdade de Medicina de Ribeirão Preto Universidade de São Paulo, 14049-900, Ribeirão Preto-SPDepartamento de Química Laboratório de Pesquisas Forenses e Genômicas Faculdade de Filosofia Ciências e Letras de Ribeirão Preto Universidade de São Paulo, 14040-901, Ribeirão Preto-SPDivisão de Imunologia Clínica Departamento de Clínica Médica Faculdade de Medicina de Ribeirão Preto Universidade de São Paulo, 14048-900, Ribeirão Preto-SPDepartamento de Patologia Faculdade de Medicina Unesp – Univ. Estadual PaulistaDepartamento de Patologia Faculdade de Medicina Unesp – Univ. Estadual PaulistaUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Fracasso, Nádia Carolina de Aguiarde Andrade, Edilene SantosWiezel, Cláudia Emília VieiraAndrade, Claudia Caixeta FrancoZanão, Lídia Renatada Silva, Mateus SpinelliMarano, Leonardo ArduinoDonadi, Eduardo AntônioC. Castelli, Erick [UNESP]Simões, Aguinaldo LuizMendes-Junior, Celso Teixeira2018-12-11T17:23:20Z2018-12-11T17:23:20Z2017-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article43-51application/pdfhttp://dx.doi.org/10.1016/j.legalmed.2016.12.013Legal Medicine, v. 25, p. 43-51.1873-41621344-6223http://hdl.handle.net/11449/17697410.1016/j.legalmed.2016.12.0132-s2.0-850094659232-s2.0-85009465923.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengLegal Medicine0,678info:eu-repo/semantics/openAccess2023-12-21T06:18:29Zoai:repositorio.unesp.br:11449/176974Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:51:31.298942Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
title |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
spellingShingle |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil Fracasso, Nádia Carolina de Aguiar Brazil Haplotypes Pigmentation SLC45A2 SNPs |
title_short |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
title_full |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
title_fullStr |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
title_full_unstemmed |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
title_sort |
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil |
author |
Fracasso, Nádia Carolina de Aguiar |
author_facet |
Fracasso, Nádia Carolina de Aguiar de Andrade, Edilene Santos Wiezel, Cláudia Emília Vieira Andrade, Claudia Caixeta Franco Zanão, Lídia Renata da Silva, Mateus Spinelli Marano, Leonardo Arduino Donadi, Eduardo Antônio C. Castelli, Erick [UNESP] Simões, Aguinaldo Luiz Mendes-Junior, Celso Teixeira |
author_role |
author |
author2 |
de Andrade, Edilene Santos Wiezel, Cláudia Emília Vieira Andrade, Claudia Caixeta Franco Zanão, Lídia Renata da Silva, Mateus Spinelli Marano, Leonardo Arduino Donadi, Eduardo Antônio C. Castelli, Erick [UNESP] Simões, Aguinaldo Luiz Mendes-Junior, Celso Teixeira |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Fracasso, Nádia Carolina de Aguiar de Andrade, Edilene Santos Wiezel, Cláudia Emília Vieira Andrade, Claudia Caixeta Franco Zanão, Lídia Renata da Silva, Mateus Spinelli Marano, Leonardo Arduino Donadi, Eduardo Antônio C. Castelli, Erick [UNESP] Simões, Aguinaldo Luiz Mendes-Junior, Celso Teixeira |
dc.subject.por.fl_str_mv |
Brazil Haplotypes Pigmentation SLC45A2 SNPs |
topic |
Brazil Haplotypes Pigmentation SLC45A2 SNPs |
description |
The Solute Carrier Family 45, Member 2 (SLC45A2) gene encodes the Membrane-Associated Transporter Protein (MATP), which mediates melanin synthesis by tyrosinase trafficking and proton transportation to melanosomes. At least two SLC45A2 coding SNPs [E272K (rs26722) and L374F (rs16891982)] were reported influencing normal variation of human pigmentation. Here we aimed at evaluating the influence of haplotypes of 12 SNPs within SLC45A2 in the determination of eye, hair and skin pigmentation in a highly admixed population sample and comparing their frequencies with the ones found in data retrieved from the 1000 Genomes Project. To achieve this goal, 12 SLC45A2 SNPs were evaluated in 288 unrelated individuals from the Ribeirão Preto city area, Southeastern Brazil. SNPs were genotyped by PCR-RFLP or Allele-specific PCR, followed by polyacrylamide gel electrophoresis. Haplotypes of each individual were inferred by two independent computational methods, PHASE and Partition-Ligation–Expectation-Maximization (PL-EM) algorithms, and 34 different haplotypes were identified. The hp9 haplotype was the most frequent (58.3%) and was associated with the presence of blond/red hair, pale skin, blue eyes and freckles. All haplotypes significantly associated with dark or light pigmentation features harbor the 374L and 374F alleles, respectively. These results emphasize the role played by haplotypes at SLC45A2 in the determination of pigmentation aspects of human populations and reinforce the relevance of SNP L374F in human pigmentation. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-03-01 2018-12-11T17:23:20Z 2018-12-11T17:23:20Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.legalmed.2016.12.013 Legal Medicine, v. 25, p. 43-51. 1873-4162 1344-6223 http://hdl.handle.net/11449/176974 10.1016/j.legalmed.2016.12.013 2-s2.0-85009465923 2-s2.0-85009465923.pdf |
url |
http://dx.doi.org/10.1016/j.legalmed.2016.12.013 http://hdl.handle.net/11449/176974 |
identifier_str_mv |
Legal Medicine, v. 25, p. 43-51. 1873-4162 1344-6223 10.1016/j.legalmed.2016.12.013 2-s2.0-85009465923 2-s2.0-85009465923.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Legal Medicine 0,678 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
43-51 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129259101749248 |