Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil

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....

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Veröffentlicht in:Birth defects research. A Clinical and molecular teratology 2012-06, Vol.94 (6), p.464-468
Hauptverfasser: Brito, Luciano Abreu, Paranaiba, Lívia Máris Ribeiro, Bassi, Camila Fernandes Silva, Masotti, Cibele, Malcher, Carolina, Schlesinger, David, Rocha, Katia Maria, Cruz, Lucas Alvizi, Bárbara, Lígia Kobayashi, Alonso, Nivaldo, Franco, Diogo, Bagordakis, Elizabete, Martelli Jr, Hercílio, Meyer, Diogo, Coletta, Ricardo D., Passos-Bueno, Maria Rita
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container_issue 6
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container_title Birth defects research. A Clinical and molecular teratology
container_volume 94
creator Brito, Luciano Abreu
Paranaiba, Lívia Máris Ribeiro
Bassi, Camila Fernandes Silva
Masotti, Cibele
Malcher, Carolina
Schlesinger, David
Rocha, Katia Maria
Cruz, Lucas Alvizi
Bárbara, Lígia Kobayashi
Alonso, Nivaldo
Franco, Diogo
Bagordakis, Elizabete
Martelli Jr, Hercílio
Meyer, Diogo
Coletta, Ricardo D.
Passos-Bueno, Maria Rita
description 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), 2012. © 2012 Wiley Periodicals, Inc.
doi_str_mv 10.1002/bdra.23011
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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. 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A Clinical and molecular teratology</title><addtitle>Birth Defects Research Part A: Clinical and Molecular Teratology</addtitle><description>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. 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A Clinical and molecular teratology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brito, Luciano Abreu</au><au>Paranaiba, Lívia Máris Ribeiro</au><au>Bassi, Camila Fernandes Silva</au><au>Masotti, Cibele</au><au>Malcher, Carolina</au><au>Schlesinger, David</au><au>Rocha, Katia Maria</au><au>Cruz, Lucas Alvizi</au><au>Bárbara, Lígia Kobayashi</au><au>Alonso, Nivaldo</au><au>Franco, Diogo</au><au>Bagordakis, Elizabete</au><au>Martelli Jr, Hercílio</au><au>Meyer, Diogo</au><au>Coletta, Ricardo D.</au><au>Passos-Bueno, Maria Rita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil</atitle><jtitle>Birth defects research. A Clinical and molecular teratology</jtitle><addtitle>Birth Defects Research Part A: Clinical and Molecular Teratology</addtitle><date>2012-06</date><risdate>2012</risdate><volume>94</volume><issue>6</issue><spage>464</spage><epage>468</epage><pages>464-468</pages><issn>1542-0752</issn><eissn>1542-0760</eissn><abstract>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), 2012. © 2012 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22511506</pmid><doi>10.1002/bdra.23011</doi><tpages>5</tpages></addata></record>
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ispartof Birth defects research. A Clinical and molecular teratology, 2012-06, Vol.94 (6), p.464-468
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1542-0760
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects 8q24 gene desert
Brazil - epidemiology
Case-Control Studies
Chromosomes, Human, Pair 8
cleft lip
Cleft Lip - ethnology
Cleft Lip - genetics
cleft palate
Cleft Palate - ethnology
Cleft Palate - genetics
common disease-common variant
Continental Population Groups
Female
Genetic Loci
Genetic Predisposition to Disease
Genome-Wide Association Study
heritability
Heterozygote
Homozygote
Humans
Male
mesenchymal stem cells
MYC transcriptional levels
Polymorphism, Single Nucleotide
Proto-Oncogene Proteins c-myc - genetics
rs1476165
rs2099897
rs987525
Transcription, Genetic
title Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil
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