Literature DB >> 16793893

Phototransduction in a transgenic mouse model of Nougaret night blindness.

Mustapha Moussaif1, William W Rubin, Vasily Kerov, Rebecca Reh, Desheng Chen, Janis Lem, Ching-Kang Chen, James B Hurley, Marie E Burns, Nikolai O Artemyev.   

Abstract

The Nougaret form of dominant stationary night blindness is linked to a G38D mutation in the rod transducin-alpha subunit (Talpha). In this study, we have examined the mechanism of Nougaret night blindness using transgenic mice expressing TalphaG38D. The biochemical, electrophysiological, and vision-dependent behavioral analyses of the mouse model revealed a unique phenotype of reduced rod sensitivity, impaired activation, and slowed recovery of the phototransduction cascade. Two key deficiencies in TalphaG38D function, its poor ability to activate PDE6 (cGMP phosphodiesterase) and decreased GTPase activity, are found to be the major mechanisms altering visual signaling in transgenic mice. Despite these defects, rod-mediated sensitivity in heterozygous mice is not decreased to the extent seen in heterozygous Nougaret patients.

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Year:  2006        PMID: 16793893      PMCID: PMC6673833          DOI: 10.1523/JNEUROSCI.1322-06.2006

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  13 in total

Review 1.  The retinal cGMP phosphodiesterase gamma-subunit - a chameleon.

Authors:  Lian-Wang Guo; Arnold E Ruoho
Journal:  Curr Protein Pept Sci       Date:  2008-12       Impact factor: 3.272

2.  Structural requirements of the photoreceptor phosphodiesterase gamma-subunit for inhibition of rod PDE6 holoenzyme and for its activation by transducin.

Authors:  Xiu-Jun Zhang; Nikolai P Skiba; Rick H Cote
Journal:  J Biol Chem       Date:  2009-11-30       Impact factor: 5.157

3.  Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness.

Authors:  Stephen H Tsang; Michael L Woodruff; Lin Jun; Vinit Mahajan; Clyde K Yamashita; Robert Pedersen; Chyuan-Sheng Lin; Stephen P Goff; Thomas Rosenberg; Michael Larsen; Debora B Farber; Steven Nusinowitz
Journal:  Hum Mutat       Date:  2007-03       Impact factor: 4.878

4.  Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.

Authors:  Takaaki Hayashi; Katsuhiro Hosono; Kentaro Kurata; Satoshi Katagiri; Kei Mizobuchi; Shinji Ueno; Mineo Kondo; Tadashi Nakano; Yoshihiro Hotta
Journal:  Doc Ophthalmol       Date:  2019-10-03       Impact factor: 2.379

5.  Transducin translocation contributes to rod survival and enhances synaptic transmission from rods to rod bipolar cells.

Authors:  Anurima Majumder; Johan Pahlberg; Kimberly K Boyd; Vasily Kerov; Saravanan Kolandaivelu; Visvanathan Ramamurthy; Alapakkam P Sampath; Nikolai O Artemyev
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-08       Impact factor: 11.205

6.  Dominant-negative Gα subunits are a mechanism of dysregulated heterotrimeric G protein signaling in human disease.

Authors:  Arthur Marivin; Anthony Leyme; Kshitij Parag-Sharma; Vincent DiGiacomo; Anthony Y Cheung; Lien T Nguyen; Isabel Dominguez; Mikel Garcia-Marcos
Journal:  Sci Signal       Date:  2016-04-12       Impact factor: 8.192

7.  Mutant Prpf31 causes pre-mRNA splicing defects and rod photoreceptor cell degeneration in a zebrafish model for Retinitis pigmentosa.

Authors:  Jun Yin; Jan Brocher; Utz Fischer; Christoph Winkler
Journal:  Mol Neurodegener       Date:  2011-07-30       Impact factor: 14.195

Review 8.  Biology and therapy of inherited retinal degenerative disease: insights from mouse models.

Authors:  Shobi Veleri; Csilla H Lazar; Bo Chang; Paul A Sieving; Eyal Banin; Anand Swaroop
Journal:  Dis Model Mech       Date:  2015-02       Impact factor: 5.758

9.  Network and atomistic simulations unveil the structural determinants of mutations linked to retinal diseases.

Authors:  Simona Mariani; Daniele Dell'Orco; Angelo Felline; Francesco Raimondi; Francesca Fanelli
Journal:  PLoS Comput Biol       Date:  2013-08-29       Impact factor: 4.475

10.  A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit.

Authors:  Gaël Manes; Pallavi Cheguru; Anurima Majumder; Béatrice Bocquet; Audrey Sénéchal; Nikolai O Artemyev; Christian P Hamel; Philippe Brabet
Journal:  PLoS One       Date:  2014-04-23       Impact factor: 3.240

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