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Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract.
Jarwar, Priya; Sheikh, Shakeel Ahmed; Waryah, Yar Muhammad; Ujjan, Ikram Uddin; Riazuddin, Saima; Waryah, Ali Muhammad; Ahmed, Zubair M.
Affiliation
  • Jarwar P; Institute of Biotechnology and Genetic Engineering, The University of Sindh, Jamshoro 76090, Pakistan.
  • Sheikh SA; Department of Molecular Biology & Genetics, Liaquat University of Medical and Health Sciences, Jamshoro 76090, Pakistan.
  • Waryah YM; Department of Molecular Biology & Genetics, Liaquat University of Medical and Health Sciences, Jamshoro 76090, Pakistan.
  • Ujjan IU; Department of Otorhinolaryngology Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, MD 21201, USA.
  • Riazuddin S; Scientific Ophthalmic and Research Laboratory, Sindh Institute of Ophthalmology and Visual Sciences, Hyderabad 71500, Pakistan.
  • Waryah AM; Department of Pathology, Liaquat University of Medical and Health Sciences, Jamshoro 76090, Pakistan.
  • Ahmed ZM; Department of Molecular Biology & Genetics, Liaquat University of Medical and Health Sciences, Jamshoro 76090, Pakistan.
Int J Mol Sci ; 22(19)2021 Sep 30.
Article in En | MEDLINE | ID: mdl-34638995
Hereditary congenital cataract (HCC) is clinically and genetically heterogeneous. We investigated HCC that segregates in three inbred families (LUCC03, LUCC16, and LUCC24). Ophthalmological examinations revealed cataracts with variability related to the age of onset segregating in a recessive manner in these families. Exome sequencing of probands identified a novel homozygous c.2710delG;p.(Val904Cysfs*36) EPHA2 variant in LUCC03 and a known homozygous c.2353G>A;p.(Ala785Thr) EPHA2 variant in the other two recessive families. EPHA2 encodes a transmembrane tyrosine kinase receptor, which is primarily involved in membrane-transport, cell-cell adhesion, and repulsion signaling processes. Computational structural modeling predicts that substitution of a threonine for an alanine p.(Ala785Thr) results in the formation of three new hydrogen bonds with the neighboring residues, which causes misfolding of EPHA2 in both scenarios. Insights from our study will facilitate counseling regarding the molecular and phenotypic landscape of EPHA2-related HCC.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cataract / Consanguinity / Mutation, Missense / Receptor, EphA2 / Alleles Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Int J Mol Sci Year: 2021 Type: Article Affiliation country: Pakistan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cataract / Consanguinity / Mutation, Missense / Receptor, EphA2 / Alleles Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Int J Mol Sci Year: 2021 Type: Article Affiliation country: Pakistan