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Background

Congenital hereditary endothelial dystrophy (CHED) is a rare form of corneal dystrophy caused by SLC4A11 gene variations. This study aims to find the genetic alterations in SLC4A11, in two Indian familial CHED cases with affected members n = 3 and n = 2 respectively and five sporadic CHED cases using direct sequencing, followed by in silico analysis and characterization of the identified variants.

Results

All three affected members of the first CHED family were identified with a novel homozygous c.1514C > G (p.Ser489Trp) variation while second family showed presence of a compound heterozygous variation c.529A > C (p.Arg161Arg) + c.2461insT (p.Val805fs). Among five sporadic cases, two showed novel changes, homozygous c.1487G > T (p.Ser480Ile) and c.620-2A > G, while the other one had previously reported homozygous c.2653C > T (p.Arg869Cys) variation. The remaining two cases did not reveal the presence of SLC4A11-related pathogenic variations. The identified variations were excluded from the Indian control (n = 80). In silico analysis using homology-based protein modeling and pathogenicity prediction tools, which revealed these alterations as pathogenic, changing their protein stability, local flexibility, residue contact clashes, and the hydrogen bond interactions.

Conclusions

This study contributed to the CHED mutational spectrum, adding four novel variations and confirming a previously reported one. It demonstrates different type of variations in CHED cases, including coding, non-coding, homozygous, synonymous, and compound heterozygous variations. The identified variations revealed different degrees of pathogenic effects in silico. Moreover, two sporadic cases could not be identified with pathogenic variation emphasizing the involvement of other genes or genetic mechanisms."xsd:string
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http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Verma A."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Singh V."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Kannabiran C."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Prasad D."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Chaurasia S."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Salman M."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/author"Ramappa M."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/name"Orphanet J Rare Dis"xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/pages"361"xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/title"Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy."xsd:string
http://purl.uniprot.org/citations/36115991http://purl.uniprot.org/core/volume"17"xsd:string
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