Literature DB >> 19161160

An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1).

Barbara Franke1, Sita H H M Vermeulen, Regine P M Steegers-Theunissen, Marieke J Coenen, Mascha M V A P Schijvenaars, Hans Scheffer, Martin den Heijer, Henk J Blom.   

Abstract

BACKGROUND: Spina bifida is a class of neural tube defects, which are congenital malformations of the central nervous system with a prevalence of 0.5 to 12 per 1000 births globally. In this article we attempt to identify genes related to folate and its metabolic pathways that are involved in the etiology of spina bifida.
METHODS: We selected 50 folate metabolism-related genes and genotyped polymorphisms in those genes. Eighty-seven polymorphisms in 45 genes passed quality controls. Associations with spina bifida were investigated in 180 patients and 190 controls. For those polymorphisms that were nominally associated with spina bifida risk, the relation with serum and red blood cell folate, vitamin B(12), and homocysteine was evaluated in controls.
RESULTS: A polymorphism in CUBN was significantly associated with decreased spina bifida risk, after correction for multiple testing, and was related to increased vitamin B(12) (p = 0.039) and red blood cell folate (p = 0.001). The CUBN gene encodes the intrinsic factor-cobalamin receptor (or cubilin), a peripheral membrane protein that acts as a receptor for intrinsic factor-vitamin B(12) complexes. Vitamin B(12) is an important cofactor in the folate metabolism, and low B(12) status in mothers has been linked to neural tube defects in children. Other interesting findings include nominally significant associations with polymorphisms in TRDMT1, ALDH1L1, SARDH, and SLCA19A1 (RFC1).
CONCLUSION: Our study indicates interesting new candidate genes and functional pathways for further study and confirms earlier findings. None of the genes CUBN, TRDMT1, ALDH1L1, or SARDH have been investigated previously for association with spina bifida. (c) 2009 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19161160     DOI: 10.1002/bdra.20556

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  33 in total

1.  Association between ALDH1L1 gene polymorphism and neural tube defects in the Chinese Han population.

Authors:  Lihua Wu; Xiaolin Lu; Jin Guo; Ting Zhang; Fang Wang; Yihua Bao
Journal:  Neurol Sci       Date:  2016-03-18       Impact factor: 3.307

Review 2.  Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturned.

Authors:  Kit Sing Au; Tina O Findley; Hope Northrup
Journal:  Am J Med Genet A       Date:  2017-09-25       Impact factor: 2.802

3.  Associations between maternal genotypes and metabolites implicated in congenital heart defects.

Authors:  Shimul Chowdhury; Charlotte A Hobbs; Stewart L MacLeod; Mario A Cleves; Stepan Melnyk; S Jill James; Ping Hu; Stephen W Erickson
Journal:  Mol Genet Metab       Date:  2012-09-27       Impact factor: 4.797

4.  Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.

Authors:  Michelle R O'Byrne; Kit Sing Au; Alanna C Morrison; Jone-Ing Lin; Jack M Fletcher; Kathryn K Ostermaier; Gayle H Tyerman; Sabine Doebel; Hope Northrup
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-08

5.  Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects.

Authors:  F Pangilinan; A Mitchell; J VanderMeer; A M Molloy; J Troendle; M Conley; P N Kirke; M Sutton; J M Sequeira; E V Quadros; J M Scott; J L Mills; L C Brody
Journal:  J Med Genet       Date:  2010-06-24       Impact factor: 6.318

6.  Prevention of neural tube defects in Lrp2 mutant mouse embryos by folic acid supplementation.

Authors:  Julia A Sabatino; Bethany A Stokes; Irene E Zohn
Journal:  Birth Defects Res       Date:  2017-01-20       Impact factor: 2.344

Review 7.  One-carbon metabolism and folate transporter genes: Do they factor prominently in the genetic etiology of neural tube defects?

Authors:  John W Steele; Sung-Eun Kim; Richard H Finnell
Journal:  Biochimie       Date:  2020-02-13       Impact factor: 4.079

8.  Maternal and infant gene-folate interactions and the risk of neural tube defects.

Authors:  Analee J Etheredge; Richard H Finnell; Suzan L Carmichael; Edward J Lammer; Huiping Zhu; Laura E Mitchell; Gary M Shaw
Journal:  Am J Med Genet A       Date:  2012-08-17       Impact factor: 2.802

9.  Cubilin, a high affinity receptor for fibroblast growth factor 8, is required for cell survival in the developing vertebrate head.

Authors:  Olivier Cases; Aitana Perea-Gomez; Diego P Aguiar; Anders Nykjaer; Sabine Amsellem; Jacqueline Chandellier; Muriel Umbhauer; Silvia Cereghini; Mette Madsen; Jérôme Collignon; Pierre Verroust; Jean-François Riou; Sophie E Creuzet; Renata Kozyraki
Journal:  J Biol Chem       Date:  2013-04-16       Impact factor: 5.157

Review 10.  Genetics of human neural tube defects.

Authors:  Nicholas D E Greene; Philip Stanier; Andrew J Copp
Journal:  Hum Mol Genet       Date:  2009-10-15       Impact factor: 6.150

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.