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Publication : Overexpression of human γC-crystallin 5 bp duplication disrupts lens morphology in transgenic mice.

First Author  Ma Z Year  2011
Journal  Invest Ophthalmol Vis Sci Volume  52
Issue  8 Pages  5369-75
PubMed ID  21436266 Mgi Jnum  J:181433
Mgi Id  MGI:5311306 Doi  10.1167/iovs.11-7168
Citation  Ma Z, et al. (2011) Overexpression of human gammaC-crystallin 5 bp duplication disrupts lens morphology in transgenic mice. Invest Ophthalmol Vis Sci 52(8):5369-75
abstractText  PURPOSE: To delineate the molecular mechanisms underlying autosomal dominant congenital cataracts caused by a 5 bp duplication in human CRYGC. METHODS: c.119_123dup (CRYGC5bpd) and wild-type human gammaC-crystallin (CRYGC) were expressed in transgenic mouse lenses by the chicken betaB1-crystallin promoter. Lenses were characterized histologically, by real-time PCR, SDS-PAGE, and Western blot. pET and Tet-on expression systems were used to express human CRYGC and CRYGC5bpd proteins in Escherichia coliand HeLa cells, respectively. RESULTS: Transgenic expression of CRYGC5bpd mutant gammaC-crystallin results in nuclear cataracts in which lens fiber cells begin to show variable degrees of degeneration and vacuolization by postnatal day 21. By 6 weeks of age all CRYGC5bpd lenses exhibit abnormalities of varying severity, comprising large vacuoles in cortical fiber cells, swelling and disorganization of fiber cells, and defective fiber cell migration and elongation. Levels of CRYGC5bpd mRNA are 3.7- and 14.1-fold higher than endogenous Crygc mRNA in postnatal day 1 and 6-week CRYGC5bpd mice lens, respectively. Crygc, Crygb, Crybb2, and Crybb3 mRNA levels are decreased in CRYGC5bpd mice compared with wild-type and CRYGC mice. Both wild-type and mutant human gammaC crystallin are uniformly distributed in the cytosol of HeLa cells, but CRYGC5bpd is degraded when expressed in E. coli BL21(DE3). CONCLUSIONS: Transgenic expression of mutant CRYGC5bpd gamma-crystallin at near-physiological levels causes lens opacities and fiber cell defects, confirming the pathogenicity of this mutation. These results further suggest that HCG5pbd gamma-crystallin causes cataracts through a direct toxic or developmental effect on lens cells causing damaged microstructure rather than through formation of HMW aggregates with resultant light scattering.
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