Functional reassessment of PAX6 single nucleotide variants by in vitro splicing assay View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-03

AUTHORS

Alexandra Yu. Filatova, Tatiana A. Vasilyeva, Andrey V. Marakhonov, Anna A. Voskresenskaya, Rena A. Zinchenko, Mikhail Yu. Skoblov

ABSTRACT

Nucleotide variants that disrupt normal splicing might be the cause of a large number of diseases. Nevertheless, because of the complexity of splicing regulation, it is not always possible to accurately predict the effect of nucleotide sequence changes on splicing events and mRNA structure. Thereby, a number of newly identified nucleotide variants are falsely classified as VUS (a variant of uncertain significance). In the present study we used the minigene assay to analyze the functional consequences of six intronic (c.142-5T>G, c.142-14C>G, c.142-64A>C, c.141+4A>G, c.1032+ 6T>G, c.682+4delA), one missense (c.140A>G) and one synonymous (c.174C>T) variants in the PAX6 gene found in patients with congenital aniridia. We revealed that all except one (c.142-64A>C) variants lead to the disruption of normal splicing patterns resulting in premature termination codon formation followed by mRNA degradation through the nonsense mediated decay pathway. This produces a null allele of the PAX6 gene. That allowed us to reclassify the analyzed variants as loss-of-function and to establish their functional role. More... »

PAGES

488-493

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41431-018-0288-y

DOI

http://dx.doi.org/10.1038/s41431-018-0288-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1107575658

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30315214


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