Study of folate receptor genes in nonsyndromic familial and sporadic cleft lip with or without cleft palate cases

Am J Med Genet A. 2005 Jan 30;132A(3):302-4. doi: 10.1002/ajmg.a.30469.

Abstract

Folate receptor family members (FOLRs) mediate the delivery of 5-methyltetrahydrofolate to the interior of, out of within, or between cells in a process known as potocytosis. Three FOLRs and a pseudogene map to 11q13.4. The aim of this study was to verify whether FOLRs could be responsible for the onset of nonsyndromic cleft lip with or without cleft palate (CL/P). Linkage and linkage disequilibrium between genetic markers and disorder were analyzed. Patients and their mothers from 71 familial CL/P pedigrees and 75 sporadic cases from Italian population were investigated by PCR-SSCP analysis. Data from mutation scanning allowed us to find only a silent mutation in FOLR1 present in a mother and her child. Our findings do not support FOLR1 and FOLR2 genes in the onset of CL/P.

MeSH terms

  • Carrier Proteins / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 11 / genetics
  • Cleft Lip / complications
  • Cleft Lip / genetics*
  • Cleft Lip / pathology
  • Cleft Palate / complications*
  • Family Health
  • Female
  • Folate Receptor 1
  • Folate Receptors, GPI-Anchored
  • Humans
  • Linkage Disequilibrium
  • Lod Score
  • Male
  • Microsatellite Repeats
  • Multigene Family / genetics
  • Pedigree
  • Receptors, Cell Surface / genetics*
  • Syndrome

Substances

  • Carrier Proteins
  • FOLR1 protein, human
  • Folate Receptor 1
  • Folate Receptors, GPI-Anchored
  • Receptors, Cell Surface

Grants and funding