FIELD: biotechnology.
SUBSTANCE: invention is intended for detecting mutation c.1121G>A (p.Trp374*) of CLIC5 gene causing autosomal recessive deafness-103. Method for DNA diagnosis of autosomal recessive deafness-103 (DFNB103), involving detection of nonsense mutation c.1121G>A(p.Trp374*) of CLIC5 gene, for which genomic DNA is extracted, PCR-RFLP analysis is carried out using the following original primers: (F) – 5'-CGCAACTATGATATCCCGGCTGAGATGACA-3', (R) – 5'-TGCTGGTATCATGGGAACTCCA-3' and restriction endonuclease Bsc4I. As a result of presence on electrophoregram of 293-bp fragment, carriage of the pathogenic allele in the homozygous state is diagnosed, which corresponds to positive DNA-diagnostics on DFNB103.
EFFECT: disclosed method is developed based on the obtained results of long-term molecular-genetic studies of neurosensory hearing disorders in Yakutia and enables fast and high-accuracy confirmation of autosomal recessive deafness-103 (DFNB103; OMIM#607293) caused by nonsense mutation c_1121G>A (p_Trp374*) of CLIC5 gene.
1 cl, 2 dwg, 7 tbl, 7 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF DETECTING MUTATIONS OF GJB2 GENE CAUSING AUTOSOMAL-RECESSIVE DEAFNESS 1A TYPE | 2017 |
|
RU2688180C1 |
METHOD FOR DETECTING 17 GJB2 AND GJB6 GENE MUTATIONS ACCOMPANYING NONSYNDROMIC DEAFNESS | 2010 |
|
RU2448163C2 |
METHOD OF DNA DIAGNOSIS OF CONGENITAL CATARACT (CTRCT18) | 2017 |
|
RU2648464C1 |
METHOD FOR SIMULTANEOUS DIAGNOSIS OF HEREDITARY DISEASES | 2015 |
|
RU2627115C2 |
METHOD FOR DETECTION OF MUTATIONS INGJB2 GENE ACCOMPANYING WITH DEVELOPMENT OF NONSYNDROMAL AUTOSOMAL-RECESSIVE DEAFNESS | 2006 |
|
RU2317547C1 |
METHOD FOR DIAGNOSING MUTATION C.-23+1G>A (RS80338940) OF THE GJB2 GENE | 2020 |
|
RU2746055C1 |
DIAGNOSTIC TECHNIQUE FOR THE 167DELT (RS80338942) MUTATION OF THE GJB2 GENE | 2020 |
|
RU2739943C1 |
DIAGNOSTIC TECHNIQUE OF 35DELG (RS80338939) MUTATION OF GJB2 GENE | 2020 |
|
RU2739889C1 |
METHOD FOR DIAGNOSING 3-M SYNDROME YAKUT POPULATION | 2006 |
|
RU2315310C1 |
METHOD FOR REVEALING c-53-2A>G MUTATION IN PRESTIN GENE (SLC26A5) CAUSING DEVELOPMENT OF NON-SYNDROME-BASED AUTSOMAL-RECESSIVE DEAFNESS | 2012 |
|
RU2505608C1 |
Authors
Dates
2020-07-22—Published
2019-12-12—Filed