Identification and Functional Characterization of Mutation in IFYCO1/I in Families with Congenital Cataract

• Published in: Life (Basel, Switzerland) Switzerland), 2023-08, Vol.13 (8)
• Main Authors: Ullah, Muhammad Ikram, Rehman, Zaira, Dad, Rubina, Alsrhani, Abdullah, Shakil, Muhammad, Ghanem, Heba Bassiony, Alameen, Ayman Ali Mohammed, Elsadek, Mohamed Farouk, Eltayeb, Lienda Bashier, Ullah, Sajjad, Atif, Muhammad
• Format: Article
• Language: English
• Subjects: Cataract; Children; Diagnosis; Diseases; DNA sequencing; Gene mutations; Genetic aspects; Genetic disorders; Genetic screening; Methods; Nucleotide sequencing; Pediatric research
• ISSN: 2075-1729; 2075-1729
• DOI: 10.3390/life13081788

Congenital cataract (CC) causes a third of the cases of treatable childhood blindness worldwide. CC is a disorder of the crystalline lens which is established as clinically divergent and has complex heterogeneity. This study aimed to determine the genetic basis of CC. Whole blood was obtained from four consanguineous families with CC. Genomic DNA was extracted from the blood, and the combination of targeted and Sanger sequencing was used to identify the causative gene. The mutations detected were analyzed in silico for structural and protein–protein interactions to predict their impact on protein activities. The sequencing found a known FYCO1 mutation (c.2206C>T; p.Gln736Term) in autosomal recessive mode in families with CC. Co-segregation analysis showed affected individuals as homozygous and carriers as heterozygous for the mutation and the unaffected as wild-type. Bioinformatics tools uncovered the loss of the Znf domain and structural compactness of the mutant protein. In conclusion, a previously reported nonsense mutation was identified in four consanguineous families with CC. Structural analysis predicted the protein as disordered and coordinated with other structural proteins. The autophagy process was found to be significant for the development of the lens and maintenance of its transparency. The identification of these markers expands the scientific knowledge of CC; the future goal should be to understand the mechanism of disease severity. Ascertaining the genetic etiology of CC in a family member facilitates establishing a molecular diagnosis, unlocks the prospect of prenatal diagnosis in pregnancies, and guides the successive generations by genetic counseling.