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Polymorphisms of the maternal Slug gene in fetal neural tube defects in a Chinese population 被引量:1

Polymorphisms of the maternal Slug gene in fetal neural tube defects in a Chinese population
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摘要 Several studies have demonstrated that Slug,which encodes a zinc finger of the Snail family of transcription factors,is a potential risk factor for neural tube defects.Neural tube defects tend to occur with a high rate in Shanxi province,China.The present case-control study investigated genotypic distributions and allele frequencies of Slug C1548A polymorphisms in DNA samples from59 women with a history of neural tube defect pregnancies and 73 controls during the same period from Shanxi Province,China.Results demonstrated that women with a history of neural tube defect pregnancies had significantly greater genotypic distributions of Slug AA genotypes and A allele frequencies compared with controls,and A allele Slug C1548A was a risk factor for neural tube defects(odds ratio = 3.444;95% confidence interval;2.021-5.868,P 〈 0.05).Three-dimensional structure prediction revealed that Slug C1548A resulted in transition of aspartic acid into glutamate at position 119.This indicated that these mutations could lead to damaged protein structure and function.These findings suggest that Slug C1548A gene polymorphism is closely related to neural tube defects in a population of Han Chinese origin from Shanxi Province,China Several studies have demonstrated that Slug,which encodes a zinc finger of the Snail family of transcription factors,is a potential risk factor for neural tube defects.Neural tube defects tend to occur with a high rate in Shanxi province,China.The present case-control study investigated genotypic distributions and allele frequencies of Slug C1548A polymorphisms in DNA samples from59 women with a history of neural tube defect pregnancies and 73 controls during the same period from Shanxi Province,China.Results demonstrated that women with a history of neural tube defect pregnancies had significantly greater genotypic distributions of Slug AA genotypes and A allele frequencies compared with controls,and A allele Slug C1548A was a risk factor for neural tube defects(odds ratio = 3.444;95% confidence interval;2.021-5.868,P 〈 0.05).Three-dimensional structure prediction revealed that Slug C1548A resulted in transition of aspartic acid into glutamate at position 119.This indicated that these mutations could lead to damaged protein structure and function.These findings suggest that Slug C1548A gene polymorphism is closely related to neural tube defects in a population of Han Chinese origin from Shanxi Province,China
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2010年第17期1342-1346,共5页 中国神经再生研究(英文版)
基金 the National Key Project of Scientific and Technical Supporting Pro-grams funded by the Ministry of Science & Technology of China, No. 2007BA107A02 the National Basic Research Program of China (973 Program), No. 2007CB511902 Shanxi Scholarship Council of China, No. 2008-48 the Natural Science Foundation of Shanxi Province, No. 2010011049-2
关键词 neural tube defects SLUG single nucleotide polymorphisms protein modeling neural tube defects Slug single nucleotide polymorphisms protein modeling
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  • 1van der Put NM,Steegers-Theunissen RP,Frosst P,et al.Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida.Lancet.1995;346(8982):1070-1071.
  • 2Botto LD,Moore CA,Khoury MJ,et al.Neural-tube defects.N Engl J Med.1999;341(20):1509-1519.
  • 3De Marco P,Calevo MG,Moroni A,et al.Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.J Hum Genet.2002;47(6):319-324.
  • 4Greene ND,Stanier P,Copp AJ.Genetics of human neural tube defects.Hum Mol Genet.2009;18(R2):R113-129.
  • 5Koch MC,Stegmann K,Ziegler A,et al.Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population.Eur J Pediatr.1998;157(6):487-492.
  • 6Shang Y,Zhao H,Niu B,et al.Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China.Birth Defects Res A Clin Mol Teratol.2008;82(1):3-7.
  • 7Stegmann K,Boecker J,Kosan C,et al.Human transcription factor SLUG:mutation analysis in patients with neural tube defects and identification of a missense mutation(D119E)in the Slug subfamily-defining region.Mutat Res.1999;406(2-4):63-69.
  • 8Stegmann K,Boecker J,Richter B,et al.A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects.Teratology.2001;63(5):167-175.
  • 9Stegmann K,Ziegler A,Ngo ET,et al.Linkage disequilibrium of MTHFR genotypes 677C/T-1298NC in the German population and association studies in probands with neural tube defects(NTD).Am J Med Genet.1999;87(1):23-29.
  • 10Boyles AL,Billups AV,Deak KL,et al.Neural tube defects and folate pathway genes:family-based association tests of gene-gene and gene-environment interactions.Environ Health Perspect.2006;114(10):1547-1552.

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