Skip to main content
Top
Published in: Neurological Sciences 11/2014

01-11-2014 | Original Article

Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population

Authors: Ou-Yan Shi, Hui-Yun Yang, Yong-Ming Shen, Wei Sun, Chun-You Cai, Chun-Quan Cai

Published in: Neurological Sciences | Issue 11/2014

Login to get access

Abstract

Neural tube defects (NTDs) are the most common and severe malformations of the central nervous system. The association of single nucleotide polymorphisms (SNPs) of the Frizzled 3 (FZD3) and Frizzled 6 (FZD6) genes and NTDs in the Han population of northern China was principally studied. One synonymous SNP (rs2241802) in FZD3 gene and three nonsynonymous SNPs (rs827528, rs3808553 and rs12549394) in FZD6 gene were analyzed by polymerase chain reaction (PCR) and sequencing methods in 135 NTD patients and 135 normal controls. The allele, genotype and haplotype frequencies were calculated and analyzed to examine the relationship between FZD3/FZD6 SNPs and NTDs. Both T allele and TT genotype frequencies of the FZD6 rs3808553 loci in the NTDs group were significantly higher than those in the controls, and children with T allele and TT genotype were associated with increased NTDs risk (OR = 1.575, 95 % CI 1.112–2.230, P = 0.010 and OR = 2.811, 95 % CI 1.325–5.967, P = 0.023, respectively). There were no differences among different genotypes or alleles in other three SNPs. Haplotypes A-G-C and A-T-C in FZD6 were found associated with NTDs in the case–control study (OR = 0.560, 95 % CI 0.378–0.830, P = 0.004 and OR = 1.670, 95 % CI 1.126–2.475, P = 0.011, respectively). The rs3808553 of FZD6 is obviously associated with NTDs in Han population of northern China. The TT genotype may increase risk for NTDs.
Appendix
Available only for authorised users
Literature
1.
go back to reference Cai C, Zhang Q, Yang W, Shen C (2008) Giant congenital melanocytic nevus coexistent with Chiari II malformation. Neuropediatrics 39(5):272–275PubMedCrossRef Cai C, Zhang Q, Yang W, Shen C (2008) Giant congenital melanocytic nevus coexistent with Chiari II malformation. Neuropediatrics 39(5):272–275PubMedCrossRef
2.
go back to reference Rossi A, Cama A, Piatelli G, Ravegnani M, Biancheri R, Tortori-Donati P (2004) Spinal dysraphism: MR imaging rationale. J Neuroradiol 31(1):3–24PubMedCrossRef Rossi A, Cama A, Piatelli G, Ravegnani M, Biancheri R, Tortori-Donati P (2004) Spinal dysraphism: MR imaging rationale. J Neuroradiol 31(1):3–24PubMedCrossRef
3.
go back to reference Beaudin AE, Stover PJ (2009) Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview. Birth Defects Res A Clin Mol Teratol 85(4):274–284PubMedCrossRef Beaudin AE, Stover PJ (2009) Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview. Birth Defects Res A Clin Mol Teratol 85(4):274–284PubMedCrossRef
4.
go back to reference De Marco P, Merello E, Calevo MG, Mascelli S, Raso A, Cama A, Capra V (2006) Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G. A polymorphism for neural tube defect risk. J Hum Genet 51(2):98–103PubMedCrossRef De Marco P, Merello E, Calevo MG, Mascelli S, Raso A, Cama A, Capra V (2006) Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G. A polymorphism for neural tube defect risk. J Hum Genet 51(2):98–103PubMedCrossRef
5.
go back to reference De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V (2003) Reduced folate carrier polymorphism (80A/G) and neural tube defects. Eur J Hum Genet 11(3):245–252PubMedCrossRef De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V (2003) Reduced folate carrier polymorphism (80A/G) and neural tube defects. Eur J Hum Genet 11(3):245–252PubMedCrossRef
6.
go back to reference Kibar Z, Capra V, Gros P (2007) Toward understanding the genetic basis of neural tube defects. Clin Genet 71(4):295–310PubMedCrossRef Kibar Z, Capra V, Gros P (2007) Toward understanding the genetic basis of neural tube defects. Clin Genet 71(4):295–310PubMedCrossRef
7.
go back to reference O’leary VB, Pangilinan F, Cox C, Parle-McDermott A, Conley M, Molloy AM, Kirke PN, Mills JL, Brody LC, Scott JM, Members of the Birth Defects Research Group (2006) Reduced folate carrier polymorphisms and neural tube defect risk. Mol Genet Metab 87(4):364–369PubMedCrossRef O’leary VB, Pangilinan F, Cox C, Parle-McDermott A, Conley M, Molloy AM, Kirke PN, Mills JL, Brody LC, Scott JM, Members of the Birth Defects Research Group (2006) Reduced folate carrier polymorphisms and neural tube defect risk. Mol Genet Metab 87(4):364–369PubMedCrossRef
8.
go back to reference Van der Linden IJ, Afman LA, Heil SG, Blom HJ (2006) Genetic variation in genes of folate metabolism and neural-tube defect risk. Proc Nutr Soc 65(2):204–215PubMedCrossRef Van der Linden IJ, Afman LA, Heil SG, Blom HJ (2006) Genetic variation in genes of folate metabolism and neural-tube defect risk. Proc Nutr Soc 65(2):204–215PubMedCrossRef
9.
go back to reference De Marco P, Merello E, Capra V (2011) Neural tube defects: genetic causes and prevention. Biofactor 37(4):261–268CrossRef De Marco P, Merello E, Capra V (2011) Neural tube defects: genetic causes and prevention. Biofactor 37(4):261–268CrossRef
10.
go back to reference Bartsch O, Kirmes I, Thiede A, Lechno S, Gocan H, Florian IS, Haaf T, Zechner U, Sabova L, Horn F (2012) Novel VANGL1 gene mutations in 144 Slovakian, Romanian and German patients with neural tube defects. Mol Syndromol 3(2):76–81PubMedCentralPubMed Bartsch O, Kirmes I, Thiede A, Lechno S, Gocan H, Florian IS, Haaf T, Zechner U, Sabova L, Horn F (2012) Novel VANGL1 gene mutations in 144 Slovakian, Romanian and German patients with neural tube defects. Mol Syndromol 3(2):76–81PubMedCentralPubMed
11.
go back to reference Kibar Z, Bosoi CM, Kooistra M, Salem S, Finnell RH, De Marco P, Merello E, Bassuk AG, Capra V, Gros P (2009) Novel mutations in VANGL1 in neural tube defects. Hum Mutat 30(7):E706–E715PubMedCentralPubMedCrossRef Kibar Z, Bosoi CM, Kooistra M, Salem S, Finnell RH, De Marco P, Merello E, Bassuk AG, Capra V, Gros P (2009) Novel mutations in VANGL1 in neural tube defects. Hum Mutat 30(7):E706–E715PubMedCentralPubMedCrossRef
12.
go back to reference Kibar Z, Torban E, McDearmid JR, Reynolds A, Berghout J, Mathieu M, Kirillova I, De Marco P, Merello E, Hayes JM, Wallingford JB, Drapeau P, Capra V, Gros P (2007) Mutations in VANGL1 associated with neural-tube defects. N Engl J Med 356(14):1432–1437PubMedCrossRef Kibar Z, Torban E, McDearmid JR, Reynolds A, Berghout J, Mathieu M, Kirillova I, De Marco P, Merello E, Hayes JM, Wallingford JB, Drapeau P, Capra V, Gros P (2007) Mutations in VANGL1 associated with neural-tube defects. N Engl J Med 356(14):1432–1437PubMedCrossRef
13.
go back to reference Kibar Z, Salem S, Bosoi CM, Pauwels E, De Marco P, Merello E, Bassuk AG, Capra V, Gros P (2011) Contribution of VANGL2 mutations to isolated neural tube defects. Clin Genet 80(1):76–82PubMedCentralPubMedCrossRef Kibar Z, Salem S, Bosoi CM, Pauwels E, De Marco P, Merello E, Bassuk AG, Capra V, Gros P (2011) Contribution of VANGL2 mutations to isolated neural tube defects. Clin Genet 80(1):76–82PubMedCentralPubMedCrossRef
14.
go back to reference Lei YP, Zhang T, Li H, Wu BL, Jin L, Wang HY (2010) VANGL2 mutations in human cranial neural-tube defects. N Engl J Med 362(23):2232–2235PubMedCrossRef Lei YP, Zhang T, Li H, Wu BL, Jin L, Wang HY (2010) VANGL2 mutations in human cranial neural-tube defects. N Engl J Med 362(23):2232–2235PubMedCrossRef
15.
go back to reference Allache R, De Marco P, Merello E, Capra V, Kibar Z (2012) Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis. Birth Defects Res A Clin Mol Teratol 94(3):176–181PubMedCrossRef Allache R, De Marco P, Merello E, Capra V, Kibar Z (2012) Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis. Birth Defects Res A Clin Mol Teratol 94(3):176–181PubMedCrossRef
16.
go back to reference Robinson A, Escuin S, Doudney K, Vekemans M, Stevenson RE, Greene ND, Copp AJ, Stanier P (2012) Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis. Hum Mutat 33(2):440–447PubMedCrossRef Robinson A, Escuin S, Doudney K, Vekemans M, Stevenson RE, Greene ND, Copp AJ, Stanier P (2012) Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis. Hum Mutat 33(2):440–447PubMedCrossRef
18.
go back to reference Wang Y, Guo N, Nathans J (2006) The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells. J Neurosci 26(8):2147–2156PubMedCrossRef Wang Y, Guo N, Nathans J (2006) The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells. J Neurosci 26(8):2147–2156PubMedCrossRef
19.
go back to reference De Marco P, Merello E, Rossi A, Piatelli G, Cama A, Kibar Z, Capra V (2012) FZD6 is a novel gene for human neural tube defects. Hum Mutat 33(2):384–390PubMedCrossRef De Marco P, Merello E, Rossi A, Piatelli G, Cama A, Kibar Z, Capra V (2012) FZD6 is a novel gene for human neural tube defects. Hum Mutat 33(2):384–390PubMedCrossRef
20.
go back to reference Schulte G, Bryja V (2007) The Frizzled family of unconventional G-protein-coupled receptors. Trends Pharmacol Sci 28(10):518–525PubMedCrossRef Schulte G, Bryja V (2007) The Frizzled family of unconventional G-protein-coupled receptors. Trends Pharmacol Sci 28(10):518–525PubMedCrossRef
21.
go back to reference Robitaille J, MacDonald ML, Kaykas A, Sheldahl LC, Zeisler J, Dubé MP, Zhang LH, Singaraja RR, Guernsey DL, Zheng B, Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, Moon RT, Hayden MR, Goldberg YP, Samuels ME (2002) Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. Nat Genet 32(2):326–330PubMedCrossRef Robitaille J, MacDonald ML, Kaykas A, Sheldahl LC, Zeisler J, Dubé MP, Zhang LH, Singaraja RR, Guernsey DL, Zheng B, Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, Moon RT, Hayden MR, Goldberg YP, Samuels ME (2002) Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. Nat Genet 32(2):326–330PubMedCrossRef
Metadata
Title
Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population
Authors
Ou-Yan Shi
Hui-Yun Yang
Yong-Ming Shen
Wei Sun
Chun-You Cai
Chun-Quan Cai
Publication date
01-11-2014
Publisher
Springer Milan
Published in
Neurological Sciences / Issue 11/2014
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-014-1815-4

Other articles of this Issue 11/2014

Neurological Sciences 11/2014 Go to the issue