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GARP2 accelerates retinal degeneration in rod cGMP-gated cation channel ?-subunit knockout mice.


ABSTRACT: The Cngb1 locus-encoded ?-subunit of rod cGMP-gated cation channel and associated glutamic acid rich proteins (GARPs) are required for phototransduction, disk morphogenesis, and rod structural integrity. To probe individual protein structure/function of the GARPs, we have characterized several transgenic mouse lines selectively restoring GARPs on a Cngb1 knockout (X1-/-) mouse background. Optical coherence tomography (OCT), light and transmission electron microscopy (TEM), and electroretinography (ERG) were used to analyze 6 genotypes including WT at three and ten weeks postnatal. Comparison of aligned histology/OCT images demonstrated that GARP2 accelerates the rate of degeneration. ERG results are consistent with the structural analyses showing the greatest attenuation of function when GARP2 is present. Even 100-fold or more overexpression of GARP1 could not accelerate degeneration as rapidly as GARP2, and when co-expressed GARP1 attenuated the structural and functional deficits elicited by GARP2. These results indicate that the GARPs are not fully interchangeable and thus, likely have separate and distinct functions in the photoreceptor. We also present a uniform murine OCT layer naming nomenclature system that is consistent with human retina layer designations to standardize murine OCT, which will facilitate data evaluation across different laboratories.

SUBMITTER: DeRamus ML 

PROVIDER: S-EPMC5309851 | biostudies-other | 2017 Feb

REPOSITORIES: biostudies-other

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GARP2 accelerates retinal degeneration in rod cGMP-gated cation channel β-subunit knockout mice.

DeRamus Marci L ML   Stacks Delores A DA   Zhang Youwen Y   Huisingh Carrie E CE   McGwin Gerald G   Pittler Steven J SJ  

Scientific reports 20170215


The Cngb1 locus-encoded β-subunit of rod cGMP-gated cation channel and associated glutamic acid rich proteins (GARPs) are required for phototransduction, disk morphogenesis, and rod structural integrity. To probe individual protein structure/function of the GARPs, we have characterized several transgenic mouse lines selectively restoring GARPs on a Cngb1 knockout (X1<sup>-/-</sup>) mouse background. Optical coherence tomography (OCT), light and transmission electron microscopy (TEM), and electro  ...[more]

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