Retinal Degeneration in Mice Lacking the γ Subunit of the Rod cGMP Phosphodiesterase
Stephen H. Tsang, Peter Gouras, Clyde K. Yamashita, H Kjeldbye, John Fisher, Debora B. Farber, Stephen P. Goff
Abstract
Stephen H. Tsang, Peter Gouras, Clyde K. Yamashita, H Kjeldbye, John Fisher, Debora B. Farber, Stephen P. Goff
Abstract
The retinal cyclic guanosine 3',5'-monophosphate (cGMP) phosphodiesterase (PDE) is a key regulator of phototransduction in the vertebrate visual system. PDE consists of a catalytic core of alpha and beta subunits associated with two inhibitory gamma subunits. A gene-targeting approach was used to disrupt the mouse PDEgamma gene. This mutation resulted in a rapid retinal degeneration resembling human retinitis pigmentosa. In homozygous mutant mice, reduced rather than increased PDE activity was apparent; the PDEalphabeta dimer was formed but lacked hydrolytic activity. Thus, the inhibitory gamma subunit appears to be necessary for integrity of the photoreceptors and expression of PDE activity in vivo.
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The retinal cyclic guanosine 3',5'-monophosphate (cGMP) phosphodiesterase (PDE) is a key regulator of phototransduction in the vertebrate visual system. PDE consists of a catalytic core of alpha and beta subunits associated with two inhibitory gamma subunits. A gene-targeting approach was used to disrupt the mouse PDEgamma gene. This mutation resulted in a rapid retinal degeneration resembling human retinitis pigmentosa. In homozygous mutant mice, reduced rather than increased PDE activity was apparent; the PDEalphabeta dimer was formed but lacked hydrolytic activity. Thus, the inhibitory gamma subunit appears to be necessary for integrity of the photoreceptors and expression of PDE activity in vivo.
Key concepts: Visual phototransduction, Phosphodiesterase, Retinitis pigmentosa, Retinal degeneration, Protein subunit, Cyclic guanosine monophosphate, Guanosine, Cell biology