Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene

Eur J Med Genet. 2010 Nov-Dec;53(6):383-8. doi: 10.1016/j.ejmg.2010.08.003. Epub 2010 Sep 21.

Abstract

X-linked chronic granulomatous disease is a primary immunodeficiency caused by mutations in CYBB. Although large deletions involving CYBB are known to cause contiguous gene syndrome (CGS), only a few patients have been studied precisely at the molecular levels. Our study determined the deletion breakpoints in two patients with CGS involving CYBB by array comparative genomic hybridization and the following PCR and DNA walking studies. The deletion size was 3.5 Mb in Patient 1 and 0.8 Mb in Patient 2. There were no homologous architectural features between the telomeric and centromeric breakpoint junctions in the deletions of either patient. However, the telomeric breakpoint of Patient 2 was embedded in a stretch of low-copy repeats and the centromeric breakpoint was also embedded in a stretch of short segments with significant sequence homology. These findings suggest the potential involvement of genome architecture in stimulating genomic rearrangements in Patient 2.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Chromosome Deletion*
  • Comparative Genomic Hybridization
  • Gene Deletion*
  • Granulomatous Disease, Chronic / diagnosis
  • Granulomatous Disease, Chronic / genetics*
  • Humans
  • Male
  • Membrane Glycoproteins / deficiency
  • Membrane Glycoproteins / genetics*
  • NADPH Oxidase 2
  • NADPH Oxidases / deficiency
  • NADPH Oxidases / genetics*
  • Segmental Duplications, Genomic / genetics
  • Young Adult

Substances

  • Membrane Glycoproteins
  • CYBB protein, human
  • NADPH Oxidase 2
  • NADPH Oxidases