Literature DB >> 9727399

Canine cone transducin-gamma gene and cone degeneration in the cd dog.

N B Akhmedov1, N I Piriev, S Pearce-Kelling, G M Acland, G D Aguirre, D B Farber.   

Abstract

PURPOSE: To characterize the cDNA and the organization of the gene encoding the cone-specific gamma subunit of transducin (Tgamma c) and to examine this gene as a candidate for the recessively inherited cone photoreceptor degeneration in the cd dog.
METHODS: Canine Tgamma c cDNA was cloned and sequenced. Polymerase chain reaction (PCR) was used to define the Tgamma c gene structure, northern blot analysis to examine the level of expression of Tgamma c mRNA in control and cd-affected retinas, and immunocytochemistry to determine the presence and localization of Tgamma c in normal and cd retinas.
RESULTS: Immunocytochemical results showed Tgamma c localized to cone photoreceptor outer segments in the normal retina, whereas no Tgamma c immunoreactivity was observed in the cd retinas. However, the level of transcription and the primary structure of the cloned cDNA coding for the 69-amino acid protein were identical in retinas from wild-type and affected dogs.
CONCLUSIONS: Although Tgamma c immunoreactivity was specifically absent in the cd dog retina, no differences were detected between normal and cd retinas in the nucleotide sequence of Tgamma c mRNA or in its synthesis. These results indicate that a mutation in the Tgamma c gene may not be causally associated with the cd dog disease. These findings suggest that possible abnormalities in posttranslational modification of Tgamma c or defective assembly of the transducin alphabetagamma complex could lead to rapid degradation of Tgamma c.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9727399

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  7 in total

1.  Species-specific differences in expression of G-protein-coupled receptor kinase (GRK) 7 and GRK1 in mammalian cone photoreceptor cells: implications for cone cell phototransduction.

Authors:  E R Weiss; M H Ducceschi; T J Horner; A Li; C M Craft; S Osawa
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

2.  Gene therapy rescues cone function in congenital achromatopsia.

Authors:  András M Komáromy; John J Alexander; Jessica S Rowlan; Monique M Garcia; Vince A Chiodo; Asli Kaya; Jacqueline C Tanaka; Gregory M Acland; William W Hauswirth; Gustavo D Aguirre
Journal:  Hum Mol Genet       Date:  2010-04-08       Impact factor: 6.150

3.  Genomic evidence for rod monochromacy in sloths and armadillos suggests early subterranean history for Xenarthra.

Authors:  Christopher A Emerling; Mark S Springer
Journal:  Proc Biol Sci       Date:  2015-02-07       Impact factor: 5.349

Review 4.  The cone dysfunction syndromes.

Authors:  M Michaelides; D M Hunt; A T Moore
Journal:  Br J Ophthalmol       Date:  2004-02       Impact factor: 4.638

Review 5.  Naturally occurring animal models with outer retina phenotypes.

Authors:  Wolfgang Baehr; Jeanne M Frederick
Journal:  Vision Res       Date:  2009-04-16       Impact factor: 1.886

6.  Transient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsia.

Authors:  András M Komáromy; Jessica S Rowlan; Amanda T Parton Corr; Shelby L Reinstein; Sanford L Boye; Ann E Cooper; Amaliris Gonzalez; Britt Levy; Rong Wen; William W Hauswirth; William A Beltran; Gustavo D Aguirre
Journal:  Mol Ther       Date:  2013-04-09       Impact factor: 11.454

Review 7.  The genetics of inherited retinal disorders in dogs: implications for diagnosis and management.

Authors:  Anna Palanova
Journal:  Vet Med (Auckl)       Date:  2016-03-15
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.