Chromosomal localization of the mouse homolog of the Huntington's disease linked G8 (D4S10) marker

DNA. 1987 Oct;6(5):401-7. doi: 10.1089/dna.1987.6.401.

Abstract

The human DNA probe G8 defines D4S10, a polymorphic locus tightly linked to the Huntington's disease gene on human chromosome 4. A subclone of G8, pSC33, showed significant cross-hybridization to discrete restriction fragments in total genomic mouse DNA. The probe detected restriction fragment length polymorphisms (RFLPs) with the enzymes Taq I and Msp I, permitting chromosomal localization of the mouse G8 homolog by linkage analysis using three sets of recombinant inbred mouse strains: BXH, BXD, and AKXD. The mouse locus was mapped to the central region of chromosome 11 at 1 centiMorgan from the SPARC gene, a locus whose human counterpart is on human chromosome 5.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chromosome Mapping
  • Huntington Disease / genetics*
  • Mice
  • Mice, Inbred Strains
  • Nucleic Acid Hybridization
  • Polymorphism, Restriction Fragment Length
  • Sequence Homology, Nucleic Acid