Nonhomologous recombination between the cytochrome b558 heavy chain gene (CYBB) and LINE-1 causes an X-linked chronic granulomatous disease

Genomics. 1998 Oct 15;53(2):123-8. doi: 10.1006/geno.1998.5510.

Abstract

We cloned and characterized a genomic DNA fragment including the deletion junction of a chronic granulomatous disease patient with a 25-kb deletion extending to the 5' two-thirds of CYBB. The 3' breakpoint of the deletion exists in exon 7 of CYBB. A LINE-1 element lies at 5 kb upstream of CYBB in normal persons, and the 5' breakpoint of the deletion in the patient is in the LINE-1 element. There are no significant homologies between corresponding normal 5' and 3' regions flanking the breakpoint of the patient, so a nonhomologous recombination is the most possible mechanism for this 25-kb deletion. The analysis also reveals that the patient has a novel 30-bp duplication in the 5' flanking region of the deletion point, which was transmitted by his mother with the deletion. Furthermore we suggest that the deletion occurred in his grandfather.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Blotting, Southern
  • Cytochrome b Group / genetics*
  • Deoxyribonucleases, Type II Site-Specific / genetics
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Female
  • Granulomatous Disease, Chronic / genetics*
  • Humans
  • Interspersed Repetitive Sequences*
  • Male
  • Molecular Sequence Data
  • NADPH Oxidases*
  • Pedigree
  • Polymorphism, Genetic
  • Recombination, Genetic*
  • Sequence Analysis, DNA
  • Sequence Deletion
  • Sequence Homology, Nucleic Acid
  • X Chromosome

Substances

  • Cytochrome b Group
  • cytochrome b558
  • NADPH Oxidases
  • Deoxyribonucleases, Type II Site-Specific

Associated data

  • GENBANK/AB013904
  • GENBANK/AB013905