[Screening of mouse connexin 31 genomic clone and mapping by fluorescence in situ hybridization]

Hunan Yi Ke Da Xue Xue Bao. 2001 Dec 28;26(6):499-501.
[Article in Chinese]

Abstract

Connexin 31(Cx31) is one of the human genetic deafness disease genes. To determine the structure and function of Cx31 gene of mouse, the mouse Cx31 gene clone was screened from the genomic library with the probe obtained according to the sequence of the mouse Cx31 gene cDNA. Cx31 gene was mapped to the center of mouse chromosome 4 by fluorescence in situ hybridization. The present study lays a foundation for researches on structure and function of Cx31 gene, as well as establishment of the relative transgenic mice and gene knockout mice.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosome Mapping*
  • Cloning, Molecular
  • Connexins / genetics*
  • Deafness / genetics
  • In Situ Hybridization, Fluorescence
  • Mice
  • Mice, Knockout

Substances

  • Connexins
  • GJB3 protein, human