Transgenic Mice Carrying the H258N Mutation in the Gene Encoding the β-Subunit of Phosphodiesterase-6 (PDE6B) Provide a Model for Human Congenital Stationary Night Blindness
| Autor: | Debora B. Farber, Michael L. Woodruff, Clyde K. Yamashita, Robert Smith Pedersen, Stephen H. Tsang, Chyuan-Sheng Lin, Michael Larsen, Lin Jun, Thomas Rosenberg, Mahajan Vinit, Steven Nusinowitz, Stephen P. Goff |
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| Jazyk: | angličtina |
| Rok vydání: | 2007 |
| Předmět: |
Retinal degeneration
Adult Male Transgene DNA Mutational Analysis Mice Transgenic Biology Article chemistry.chemical_compound Mice PDE6B Night Blindness Retinitis pigmentosa Genetics medicine Electroretinography Animals Humans Transgenes Allele Genetics (clinical) Cyclic Nucleotide Phosphodiesterases Type 6 medicine.diagnostic_test Phosphoric Diester Hydrolases Retinal Degeneration Retinal medicine.disease Molecular biology Disease Models Animal chemistry Rhodopsin Mice Inbred DBA Mutation biology.protein Female sense organs |
| Popis: | Mutations in the beta-subunit of cGMP-phosphodiesterase (PDE6beta) can lead to either progressive retinal disease, such as human retinitis pigmentosa (RP), or stationary disease, such as congenital stationary night blindness (CSNB). Individuals with CSNB in the Rambusch pedigree were found to carry the H258N allele of PDE6B (MIM# 180072); a similar mutation was not found in RP patients. This report describes an individual carrying the H258N allele, who presented with generalized retinal dysfunction affecting the rod system and a locus of dysfunction at the rod-bipolar interface. Also described are preclinical studies in which transgenic mice with the H258N allele were generated to study the pathophysiological mechanisms of CSNB. While Pde6b(rd1)/Pde6b(rd1) mice have severe photoreceptor degeneration, as in human RP, the H258N transgene rescued these cells. The cGMP-PDE6 activity of dark-adapted H258N mice showed an approximate three-fold increase in the rate of retinal cGMP hydrolysis: from 130.1 nmol x min(-1) x nmol(-1) rhodopsin in wild-type controls to 319.2 nmol x min(-1) x nmol(-1) rhodopsin in mutants, consistent with the hypothesis that inhibition of the PDE6beta activity by the regulatory PDE6gamma subunit is blocked by this mutation. In the albino (B6CBA x FVB) F2 hybrid background, electroretinograms (ERG) from H258N mice were similar to those obtained from affected Rambusch family members, as well as humans with the most common form of CSNB (X-linked), demonstrating a selective loss of the b-wave with relatively normal a-waves. When the H258N allele was introduced into the DBA background, there was no evidence of selective reduction in b-wave amplitudes; rather a- and b-wave amplitudes were both reduced. Thus, factors other than the PDE6B mutation itself could contribute to the variance of an electrophysiological response. Therefore, caution is advisable when interpreting physiological phenotypes associated with the same allele on different genetic backgrounds. Nevertheless, such animals should be of considerable value in further studies of the molecular pathology of CSNB. |
| Databáze: | OpenAIRE |
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