Characterization of a mouse Cx50 mutation associated with the No2 mouse cataract

Invest Ophthalmol Vis Sci. 1999 Jul;40(8):1844-50.

Abstract

Purpose: Recently, a missense mutation in the mouse connexin 50 (Cx50) gene has been associated with the nuclear opacity 2 (No2) mouse cataract. This missense mutation (D47A) resulted in an aspartate-to-alanine substitution at amino acid position 47 in the first extracellular domain of Cx50. To better understand the role of Cx50 in the pathogenesis of congenital cataract, the functional consequences of the D47A mutation in the Xenopus oocyte expression system were studied.

Methods: D47A was constructed using polymerase chain reaction (PCR) mutagenesis. Xenopus oocytes were injected with in vitro transcribed cRNA encoding wild-type mouse Cx50 (Cx50wt), wild-type rat Cx46 (Cx46wt), D47A, or combinations of wild-type and mutant connexins. The oocytes were then devitellinized and paired. Gap junctional conductance (Gj) was measured using a dual two-microelectrode voltage-clamp technique.

Results: Homotypic oocyte pairs expressing wild-type Cx50 or Cx46 were well coupled. In contrast, oocytes injected with D47A cRNA did not form gap junctional channels when paired homotypically. To test whether the D47A mutation could interact with wild-type connexins in a dominant negative manner, oocytes were injected with equal amounts of mutant and wild-type connexin cRNA, mimicking the heterozygous condition. Expression of D47A did not inhibit the development of junctional conductance in paired oocytes induced by wild-type Cx50 or Cx46.

Conclusions: These results indicate that the D47A mutation acts as a loss-of-function mutation without strong dominant inhibition. In No2 mice, the mutation would be predicted to result in a reduction in intercellular communication, leading to cataractogenesis. It may also cause other qualitative changes such as a change in permeability for small molecules.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Western
  • Cataract / genetics*
  • Connexins / genetics*
  • Connexins / physiology
  • DNA Primers / chemistry
  • Eye Proteins / genetics*
  • Female
  • Gap Junctions / physiology
  • Mice
  • Mutagenesis, Site-Directed
  • Mutation, Missense / physiology*
  • Oocytes / physiology
  • Patch-Clamp Techniques
  • Point Mutation / physiology*
  • Polymerase Chain Reaction
  • RNA, Complementary / genetics
  • Rats
  • Xenopus laevis

Substances

  • Connexins
  • DNA Primers
  • Eye Proteins
  • RNA, Complementary
  • GJA3 protein, human
  • connexin 50