A t(4;6)(q12;p23) translocation disrupts a membrane-associated O-acetyl transferase gene (MBOAT1) in a patient with a novel brachydactyly-syndactyly syndrome

Eur J Hum Genet. 2007 Jul;15(7):743-51. doi: 10.1038/sj.ejhg.5201833. Epub 2007 Apr 18.

Abstract

Here, we report a patient with a novel brachydactyly-syndactyly syndrome and a de novo translocation 46,XY,t(4;6)(q12;p23). We mapped the breakpoint and identified genes in the breakpoint region. One of the genes on chromosome 6, the membrane-associated O-acetyl transferase gene 1 (MBOAT1), was disrupted by the breakpoint. This gene consists of 13 exons and encodes a protein of 495 amino acids. MBOAT1 is predicted to be a transmembrane protein and belongs to the superfamily of membrane-bound O-acyltransferases. These proteins transfer organic compounds, usually fatty acids, onto hydroxyl groups of membrane-embedded targets. Identification of the transferred acyl group and the target may reveal the signaling pathways altered in this novel brachydactyly-syndactyly syndrome.

Publication types

  • Case Reports

MeSH terms

  • Acetyltransferases / genetics*
  • Adult
  • Chromosomes, Human, Pair 4 / genetics*
  • Chromosomes, Human, Pair 6 / genetics*
  • Fingers / abnormalities
  • Hand Deformities, Congenital / enzymology
  • Hand Deformities, Congenital / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Membrane Proteins
  • Syndactyly / enzymology
  • Syndactyly / genetics*
  • Translocation, Genetic*

Substances

  • Membrane Proteins
  • Acetyltransferases
  • MBOAT1 protein, human