Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolution

Cytogenet Cell Genet. 1988;48(2):124-5. doi: 10.1159/000132605.

Abstract

The gene encoded at the human X-linked chronic granulomatous disease locus (cytochrome b245 beta subunit) has been mapped to the mouse X chromosome using an interspecific Mus domesticus x M. spretus cross. The localization of this gene provides detailed information on one of the proposed ancestral breakpoints that account for the divergent evolution of the mouse and human X chromosomes.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Biological Evolution
  • Chromosome Mapping*
  • Crosses, Genetic
  • Cytochrome b Group / genetics
  • DNA Probes
  • Female
  • Granulomatous Disease, Chronic / genetics*
  • Humans
  • Male
  • Mice
  • Recombination, Genetic
  • Sequence Homology, Nucleic Acid
  • Sex Chromosome Aberrations / genetics
  • Species Specificity
  • X Chromosome*

Substances

  • Cytochrome b Group
  • DNA Probes
  • cytochrome b245