MMUUTTAATTIIOONNANALYSIS OF PAX9 GENE IN AFFECTED FAMILY OF HYPODONTIA ATTENDING TERTIARY CARE HOSPITAL OF QUETTA

Abstract

Objective: To identify the phenotype and genotype of hypodontia for a Pakistani family with hypodontia and to map the genes locus responsible for this disease. Study Design: Descriptive study. Place and Duration of Study: This descriptive study was performing in human molecular genetics (HMG) laboratory of Baluchistan University of information technology, engineering and management sciences (BUITEMS). The study was of 4 months duration. Material and Methods: Blood samples (5ml) were collected from all 15 families’ members (35participant). Genomic DNA was extracted by using inorganic method. All the three coding exons of PAX9 (NM_006194) were amplified and sequenced. Sequencing of the PAX9 coding exons and splice sites showed a homozygous misses substitution in exon 3 (c. 718G>C; p.Ala240Pro) in the affected individuals of the family. Results: Intra-oral and panoramic radiographs revealed that the proband (II-1) and her father (I-1) have hypodontia denoted by the complete absence of teeth in maxillary arch, while all other family members maintained normal dentitions. The missing teeth are both upper lateral incisors (12, 22 FDI numbering) and third molars (18, 28). Mandibular arch show; retained deciduous teeth and no teeth permanent teeth missing. Pedigree construction indicated that phenotypes in this family showed an autosomal recessive segregation pattern. The sequencing of coding exons and splice sites of PAX9 gene showed a homozygous missense mutation in exon number 3 (c. 718G>C; p.Ala240Pro) in the affected individuals of the family. Conclusion: We identified a missense mutation (p.Ala240Pro) in gene PAX9 coding exon 3 in Pakistani family with hypodontia.

Keywords

• congenital
• hypodontia
• missense mutation