Literature DB >> 32869108

Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes.

Worapoj Jinda1, Aekkachai Tuekprakhon2, Wanna Thongnoppakhun1, Chanin Limwongse1,3, Adisak Trinavarat4, La-Ongsri Atchaneeyasakul5.   

Abstract

PURPOSE: Achromatopsia (ACHM) is an autosomal recessive cone disorder characterized by pendular nystagmus, photophobia, reduced visual acuity, and partial or total absence of color vision. Mutations in six genes (CNGA3, CNGB3, GNAT2, PDE6C, PDE6H, and ATF6) have been reported in ACHM. There is no information on these disease-associated genes in Thai population. This study aimed to investigate the molecular and clinical characteristics in Thai patients with ACHM.
METHODS: Seven unrelated Thai patients with ACHM were recruited. Detailed ophthalmologic examination was performed. Polymerase chain reaction (PCR)-coupled single-strand conformation polymorphism (SSCP) screening followed by Sanger sequencing was used to identify sequence variants in all exons and splice junctions of three genes (CNGA3, CNGB3, and GNAT2). The pathogenicity of the detected variants was interpreted. Segregation analysis was performed to determine variant sharing in available family members.
RESULTS: Four patients displayed different SSCP migration patterns. Sequence analysis revealed a reported pathogenic and a novel disease-associated variant in the CNGA3 gene. For the CNGB3 gene, we found two novel disease-associated variants and a reported variant of uncertain significance (VUS). Segregation analysis confirmed that the variants identified in each patient were present in the heterozygous state in their corresponding family members, which was consistent with an autosomal recessive mode of inheritance.
CONCLUSIONS: This study demonstrated the first molecular and clinical characterization of ACHM in Thai patients. The identification of disease-associated genes in a specific population leads to a personalized gene therapy benefiting those affected patients.

Entities:  

Keywords:  Achromatopsia; CNGA3; CNGB3; Disease-associated variants; Genotype–phenotype correlation

Mesh:

Substances:

Year:  2020        PMID: 32869108     DOI: 10.1007/s10792-020-01559-2

Source DB:  PubMed          Journal:  Int Ophthalmol        ISSN: 0165-5701            Impact factor:   2.031


  41 in total

1.  A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.

Authors:  Bo Chang; Tanja Grau; Susann Dangel; Ron Hurd; Bernhard Jurklies; E Cumhur Sener; Sten Andreasson; Helene Dollfus; Britta Baumann; Sylvia Bolz; Nikolai Artemyev; Susanne Kohl; John Heckenlively; Bernd Wissinger
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-03       Impact factor: 11.205

2.  Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.

Authors:  Alberta A H J Thiadens; Ville Somervuo; L Ingeborgh van den Born; Susanne Roosing; Mary J van Schooneveld; Robert W A M Kuijpers; Norka van Moll-Ramirez; Frans P M Cremers; Carel B Hoyng; Caroline C W Klaver
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-06-23       Impact factor: 4.799

3.  Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.

Authors:  S Kohl; B Baumann; M Broghammer; H Jägle; P Sieving; U Kellner; R Spegal; M Anastasi; E Zrenner; L T Sharpe; B Wissinger
Journal:  Hum Mol Genet       Date:  2000-09-01       Impact factor: 6.150

4.  Genetic etiology and clinical consequences of complete and incomplete achromatopsia.

Authors:  Alberta A H J Thiadens; Niki W R Slingerland; Susanne Roosing; Mary J van Schooneveld; Janneke J C van Lith-Verhoeven; Norka van Moll-Ramirez; L Ingeborgh van den Born; Carel B Hoyng; Frans P M Cremers; Caroline C W Klaver
Journal:  Ophthalmology       Date:  2009-07-09       Impact factor: 12.079

5.  A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.

Authors:  Susanne Kohl; Frauke Coppieters; Françoise Meire; Simone Schaich; Susanne Roosing; Christina Brennenstuhl; Sylvia Bolz; Maria M van Genderen; Frans C C Riemslag; Robert Lukowski; Anneke I den Hollander; Frans P M Cremers; Elfride De Baere; Carel B Hoyng; Bernd Wissinger
Journal:  Am J Hum Genet       Date:  2012-08-16       Impact factor: 11.025

6.  Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2).

Authors:  I A Aligianis; T Forshew; S Johnson; M Michaelides; C A Johnson; R C Trembath; D M Hunt; A T Moore; E R Maher
Journal:  J Med Genet       Date:  2002-09       Impact factor: 6.318

Review 7.  The cone dysfunction syndromes.

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

8.  Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.

Authors:  Susanne Kohl; Britta Baumann; Thomas Rosenberg; Ulrich Kellner; Birgit Lorenz; Maria Vadalà; Samuel G Jacobson; Bernd Wissinger
Journal:  Am J Hum Genet       Date:  2002-06-20       Impact factor: 11.025

9.  Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.

Authors:  Mervyn George Thomas; Rebecca Jane McLean; Susanne Kohl; Viral Sheth; Irene Gottlob
Journal:  Br J Ophthalmol       Date:  2012-07-11       Impact factor: 4.638

10.  Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.

Authors:  S Kohl; T Marx; I Giddings; H Jägle; S G Jacobson; E Apfelstedt-Sylla; E Zrenner; L T Sharpe; B Wissinger
Journal:  Nat Genet       Date:  1998-07       Impact factor: 38.330

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.