Mutations screening of selected genes involved in familial cases of skeletal disorders from khyber Pakhtunkhwa

Abstract of Study (Max 300 Words):

Introduction: Human skeletal disorders result from abnormalities in the development of bone, cartilage, and joint.A chain of intricate signaling pathways (FGF, TGFβ, BMP, and WNT etc ;) are crucial for appropriate skeletogenesis. Thehuman skeletal dysplasias result from abnormal regulation in the primary or secondary stage of these pathways as reviewed recently. Pathogenic variants of genes involved in metabolism within the cell, extracellular matrix, or regulationof transcription can result in dysregulation of cell-cell and cell-matrix signaling thereby altering cell division, differentiation, apoptosis and tissue patterning. The clinical phenotypes point to the major action of particular constituents ofthese pathways, although they work together to regulate the formation of bone, cartilage, and joint.Objective: Mutation screening of potential candidate genes in familial disorders is well established through Sangersequencing. Methodology: After getting informed written consent and approved from the Institutional Review Board (IRB), KMUPeshawar, clinical Investigations of the selected families were performed in the Hayatabad Medical Complex, Peshawar. Blood Sampling was done in EDTA tubes; DNA extruded using Organic Phenol Chloroform Method. PolymeraseChain Reaction was performed in TPersonal thermo-cycler. Primers were designed using Primers 3 Software and DNASequencing done using Bi-Directional DNA sequencing kits (ABI) and Automated DNA analyzer ABI 3730. Sequencingwas performed in the Core Facility Laboratory of Cincinnati Children Hospital Ohio, USA. BioEdit Software and ClustalWwere used for Sequence Alignment.Results: Mutation analysis of the pathogenic variant in families demonstrating autosomal recessive non-syndromic postaxial polydactyly and autosomal dominant non-syndromic brachydactyly phenotypes was performed by directsequencing of HOXD13 gene as a potential candidate. Bidirectional sequencing of HOXD13 gene including all codingexons and intron-exons boundaries in an affected and an un affected individuals of each family was performed by automated sequencer ABI 3730XL DNA Analyzer (Life Technologies, USA). However, sequencing analysis of the affectedindividuals in each family did not reveal any pathogenic variant.Conclusion: Mutations screening, for molecular pathogenicity of HOXD13 gene in affected individuals of familieswith skeletal disorders including postaxial polydactyly and brachydactyly type D phenotypes were investigated and didnot reveal pathogenic variant.