IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5

Mamm Genome. 1998 Jan;9(1):26-31. doi: 10.1007/s003359900674.

Abstract

Huntington's disease (HD) is a devastating central nervous system disorder. Even though the gene responsible has been positionally cloned recently, its etiology has remained largely unclear. To investigate potential disease mechanisms, we conducted a search for binding partners of the HD-protein huntingtin. With the yeast two-hybrid system, one such interacting factor, the huntingtin interacting protein-1 (HIP-1), was identified (Wanker et al. 1997; Kalchman et al. 1997) and the human gene mapped to 7q11.2. In this paper we demonstrate the localization of the HIP1 mouse homologue (Hip1) into a previously identified region of human-mouse synteny on distal mouse Chromosome (Chr) 5, both employing an IRS-PCR-based mapping strategy and traditional fluorescent in situ hybridization (FISH) mapping.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosome Mapping*
  • Cloning, Molecular
  • Cosmids
  • Crosses, Genetic
  • DNA-Binding Proteins*
  • Genome
  • In Situ Hybridization, Fluorescence
  • Mice
  • Nerve Tissue Proteins / genetics*
  • Polymerase Chain Reaction / methods*
  • Polymorphism, Genetic

Substances

  • DNA-Binding Proteins
  • HIP1 protein, human
  • Hap1 protein, mouse
  • Nerve Tissue Proteins