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http://purl.uniprot.org/citations/32201916http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/32201916http://www.w3.org/2000/01/rdf-schema#comment"

Background

In recent years, the elucidation of splicing abnormalities as a cause of hereditary diseases has progressed. However, there are no comprehensive reports of suspected splicing variants in the CLCN5 gene in Dent disease cases. We reproduced gene mutations by mutagenesis, inserted the mutated genes into minigene vectors, and investigated the pathogenicity and onset mechanisms of these variants.

Methods

We conducted functional splicing assays using a hybrid minigene for six suspected splicing variants (c.105G>A, c.105+5G>C, c.106-17T>G, c.393+4A>G, c.517-8A>G, c.517-3C>A) in CLCN5. We extracted information on these variants from the Human Gene Mutation Database. We reproduced minigene vectors with the insertion of relevant exons with suspected splicing variants. We then transfected these minigene vectors into cultured cells and extracted and analyzed the mRNA. In addition, we conducted in silico analysis to confirm our minigene assay results.

Results

We successfully determined that five of these six variants are pathogenic via the production of splicing abnormalities. One showed only normal transcript production and was thus suspected of not being pathogenic (c.106-17T>G).

Conclusion

We found that five CLCN5 variants disrupted the original splice site, resulting in aberrant splicing. It is sometimes difficult to obtain mRNA from patient samples because of the fragility of mRNA or its low expression level in peripheral leukocytes. Our in vitro system can be used as an alternative to in vivo assays to determine the pathogenicity of suspected splicing variants."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.org/dc/terms/identifier"doi:10.1007/s10157-020-01876-x"xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Inoue T."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Matsuo M."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Sakakibara N."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Iijima K."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Yamamura T."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Shibagaki Y."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Ichikawa D."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Nozu K."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Nagano C."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Horinouchi T."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Aoto Y."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Ishiko S."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Rossanti R."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/author"Ishimori S."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/name"Clin Exp Nephrol"xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/pages"606-612"xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/title"Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1."xsd:string
http://purl.uniprot.org/citations/32201916http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/32201916http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/32201916
http://purl.uniprot.org/citations/32201916http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/32201916
http://purl.uniprot.org/uniprot/#_B3KRR2-mappedCitation-32201916http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/32201916
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