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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.

Publication ,  Journal Article
Deak, KL; Boyles, AL; Etchevers, HC; Melvin, EC; Siegel, DG; Graham, FL; Slifer, SH; Enterline, DS; George, TM; Vekemans, M; McClay, D ...
Published in: Hum Genet
July 2005

Neural tube defects (NTDs) are common birth defects, occurring in approximately 1/1,000 births; both genetic and environmental factors are implicated. To date, no major genetic risk factors have been identified. Throughout development, cell adhesion molecules are strongly implicated in cell-cell interactions, and may play a role in the formation and closure of the neural tube. To evaluate the role of neural cell adhesion molecule 1 (NCAM1) in risk of human NTDs, we screened for novel single-nucleotide polymorphisms (SNPs) within the gene. Eleven SNPs across NCAM1 were genotyped using TaqMan. We utilized a family-based approach to evaluate evidence for association and/or linkage disequilibrium. We evaluated American Caucasian simplex lumbosacral myelomeningocele families (n=132 families) using the family based association test (FBAT) and the pedigree disequilibrium test (PDT). Association analysis revealed a significant association between risk for NTDs and intronic SNP rs2298526 using both the FBAT test (P=0.0018) and the PDT (P=0.0025). Using the HBAT version of the FBAT to look for haplotype association, all pairwise comparisons with SNP rs2298526 were also significant. A replication study set, consisting of 72 additional families showed no significant association; however, the overall trend for overtransmission of the less common allele of SNP rs2298526 remained significant in the combined sample set. In addition, we analyzed the expression pattern of the NCAM1 protein in human embryos, and while NCAM1 is not expressed within the neural tube at the time of closure, it is expressed in the surrounding and later in differentiated neurons of the CNS. These results suggest variations in NCAM1 may influence risk for human NTDs.

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Published In

Hum Genet

DOI

ISSN

0340-6717

Publication Date

July 2005

Volume

117

Issue

2-3

Start / End Page

133 / 142

Location

Germany

Related Subject Headings

  • Spinal Cord
  • Polymorphism, Single Nucleotide
  • Pedigree
  • Neural Cell Adhesion Molecules
  • Meningocele
  • Linkage Disequilibrium
  • Introns
  • Humans
  • Haplotypes
  • Genetics & Heredity
 

Citation

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Deak, K. L., Boyles, A. L., Etchevers, H. C., Melvin, E. C., Siegel, D. G., Graham, F. L., … Speer, M. C. (2005). SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Hum Genet, 117(2–3), 133–142. https://doi.org/10.1007/s00439-005-1299-7
Deak, Kristen L., Abee L. Boyles, Heather C. Etchevers, Elizabeth C. Melvin, Deborah G. Siegel, Felicia L. Graham, Susan H. Slifer, et al. “SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.Hum Genet 117, no. 2–3 (July 2005): 133–42. https://doi.org/10.1007/s00439-005-1299-7.
Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, et al. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Hum Genet. 2005 Jul;117(2–3):133–42.
Deak, Kristen L., et al. “SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.Hum Genet, vol. 117, no. 2–3, July 2005, pp. 133–42. Pubmed, doi:10.1007/s00439-005-1299-7.
Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, Speer MC. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Hum Genet. 2005 Jul;117(2–3):133–142.
Journal cover image

Published In

Hum Genet

DOI

ISSN

0340-6717

Publication Date

July 2005

Volume

117

Issue

2-3

Start / End Page

133 / 142

Location

Germany

Related Subject Headings

  • Spinal Cord
  • Polymorphism, Single Nucleotide
  • Pedigree
  • Neural Cell Adhesion Molecules
  • Meningocele
  • Linkage Disequilibrium
  • Introns
  • Humans
  • Haplotypes
  • Genetics & Heredity