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Purpose: The rdAc cat has an intronic mutation in the centrosomal 290 kDa (CEP290) gene resulting in a frameshift and a premature stop codon (c.6960 + 9 T > G, p.Ile2321AlafsTer3) predicted to truncate the protein by 157 amino acids. CEP290 mutations in human patients cause a range or phenotypes including syndromic conditions and severe childhood loss of vision while the rdAc cat has a milder phenotype. We sought to further characterize the effect of rdAc mutation on CEP290 expression. Methods: TaqMan quantitative real‐time polymerase chain reaction assays were used to compare wildtype and truncated transcript levels. Relative protein abundance was analyzed by Western blot. Immunohistochemistry (IHC) was performed to detect CEP290 protein. Results: CEP290 mutant cats show low‐level (17.4% of wildtype cats) use of the wildtype splice site and usage of the mutant splice site. Western analysis shows retina from cats homozygous for the mutation has CEP290 protein that likely comprises a combination of both wildtype and truncated protein. IHC detects CEP290 in affected and control retina labeling the region of the interconnecting cilium. Conclusions: The comparably milder phenotype of CEP290 mutant cats is likely due to the retained production of some full‐length CEP290 protein with possible functional contributions from presence of truncated protein. [ABSTRACT FROM AUTHOR]

Objectives: To determine the accuracy and precision of the Icare® TONOVET Plus rebound tonometer and the Tono‐Pen AVIA Vet™ applanation tonometer for intraocular pressure (IOP) measurement in normal ex vivo canine eyes and comparison to earlier models of these tonometers. Animals & procedures: The anterior chambers of six normal dog eyes were cannulated ex vivo. IOP was measured with the TONOVET (TV01), TONOVET Plus, Tono‐Pen Vet™, and Tono‐Pen AVIA Vet™ at manometric IOPs ranging from 5 to 70 mm Hg. Data were analyzed by linear regression, ANOVA and Bland‐Altman plots. A P value ≤.05 was considered significant. Results: Intraocular pressure values obtained using the TONOVET Plus and TV01 were significantly more accurate than with the Tono‐Pen VET and Tono‐Pen AVIA Vet, particularly at higher IOPs (30‐70 mm Hg). Accuracy was not significantly different between any of the devices in the low to normal physiologic IOP range (5‐25 mm Hg). Level of precision was high for all devices, though the TONOVET Plus was more precise than the Tono‐Pen Vet in the 5‐25 mmHg range and the TV01 was more precise than the Tono‐Pen AVIA Vet over the whole IOP range. Conclusions: All devices underestimated IOP, particularly at higher pressures. Rebound tonometers were more accurate over the full range of IOP tested and in the high IOP range; however, there were no significant differences in accuracy among devices in the physiologic IOP range. All tonometers can provide clinically useful IOP readings in dogs, but rebound and applanation tonometers should not be used interchangeably. [ABSTRACT FROM AUTHOR]