Region 8q24 Is a Susceptibility Locus for Nonsyndromic Oral Clefting in Brazil


Autoria(s): Brito, Luciano Abreu; Ribeiro Paranaiba, Livia Maris; Silva, Camila Bassi Fernandes da; Masotti, Cibele; Silva, Carolina Malcher Amorim de Carvalho; Schlesinger, David; Rocha, Katia Maria da; Cruz, Lucas Alvizi; Barbara, Ligia Kobayashi; Alonso, Nivaldo; Franco, Diogo; Bagordakis, Elizabete; Martelli, Hercilio, Jr.; Meyer, Diogo; Coletta, Ricardo D.; Bueno, Maria Rita dos Santos e Passos
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/11/2013

07/11/2013

2012

Resumo

BACKGROUND: Nonsyndromic cleft lip with or without cleft palate is a relatively common craniofacial defect with multifactorial inheritance. The association of the rs987525 single nucleotide variant, located in a gene desert at 8q24.21 region, has been consistently replicated in European populations. We performed a structured association approach combined with transcriptional analysis of the MYC gene to dissect the role of rs987525 in oral clefting susceptibility in the ethnically admixed Brazilian population. METHODS: We performed the association study conditioned on the individual ancestry proportions in a sample of 563 patients and 336 controls, and in an independent sample of 221 patients and 261 controls. The correlation between rs987525 genotypes and MYC transcriptional levels in orbicularis oris muscle mesenchymal stem cells was also investigated in 42 patients and 4 controls. RESULTS: We found a significant association in the larger sample (p = 0.0016; OR = 1.80 [95% confidence interval {CI}, 1.21-2.69], for heterozygous genotype, and 2.71 [95% CI, 1.47-4.96] for homozygous genotype). We did not find a significant correlation between rs987525 genotypes and MYC transcriptional levels (p = 0.14; r = -0.22, Spearman Correlation). CONCLUSIONS: We present a positive association of rs987525 in the Brazilian population for the first time, and it is likely that the European contribution to our population is driving this association. We also cannot discard a role of rs987515 in MYC regulation, because this locus behaves as an expression quantitative locus of MYC in another tissue. Birth Defects Research (Part A) 94:464-468, 2012. (C) 2012 Wiley Periodicals, Inc.

FAPESP/CEPID [98/14254-2]

FAPESP/CEPID

CNPq [401952/2010-S]

CNPq

Brazilian Ministry of Health

Brazilian Ministry of Health

Identificador

BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, HOBOKEN, v. 94, n. 6, supl. 1, Part 1, pp. 464-468, JUN, 2012

1542-9768

http://www.producao.usp.br/handle/BDPI/43042

10.1002/bdra.23011

http://dx.doi.org/10.1002/bdra.23011

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

HOBOKEN

Relação

BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Direitos

closedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #RS987525 #RS1476165 #RS2099897 #HERITABILITY #CLEFT LIP #CLEFT PALATE #8Q24 GENE DESERT #MYC TRANSCRIPTIONAL LEVELS #COMMON DISEASE-COMMON VARIANT #MESENCHYMAL STEM CELLS #MULTILOCUS GENOTYPE DATA #OROFACIAL CLEFTS #GENETIC-VARIANTS #CHROMOSOME 8Q24 #LIP #PALATE #POPULATION #ASSOCIATION #RISK #IRF6 #DEVELOPMENTAL BIOLOGY #TOXICOLOGY
Tipo

article

original article

publishedVersion