Developmental Genetics · 1999 · 85 citations · 21 references
MedicineGeneticsMolecular GeneticsOcular DiseaseOcular GeneticsOcular PathologyCongenital CataractLens DiseaseLens DisordersLens PathologyOcular Developmental GeneticsPediatric CataractConnexin Gene MutationsCrystallin Gene MutationsCrystallin ModificationDevelopmental CataractGenetic Modifier EffectsHereditary Cataract
Connexin alpha 3 (Cx46 or Gja3) gene targeted null mice developed lens nuclear cataracts shortly after birth. A large variance in the cataracts was observed in alpha 3 null sibs on a mixed 129SvJae X C57BL/6J F3 background. This suggested that the genetic background might influence the cataract phenotype. Therefore, we placed the alpha 3 null mutation into a 129SvJae background, and also backcrossed the mutation for six generations into 129SvJ and C57BL/6J backgrounds. While alpha 3 nulls on the two 129 backgrounds contained severe cataracts associated with gamma crystallin cleavage, alpha 3 nulls on the C57B16 background had far milder cataracts with no detectable gamma crystallin cleavage. These findings suggest that a genetic modifier exists that influences gamma crystallin stability, and that gamma crystallin breakdown is associated with severe nuclear cataracts.
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Cardiac Malformation in Neonatal Mice Lacking Connexin43
Andrew G. Reaume, Paul A. De Sousa, Sarang Kulkarni et al. · Science · 1995 · 1.2K citations
Female infertility in mice lacking connexin 37
Alexander M. Simon, Daniel A. Goodenough, En Li et al. · Nature · 1997 · 741 citations
Medicine, Genetics, Physiology +10
Disruption of α3 Connexin Gene Leads to Proteolysis and Cataractogenesis in Mice
Xiaohua Gong, En Li, George Klier et al. · Cell · 1997 · 419 citations · Full text