Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia

Guruswamy Neethirajan, Jeyabalan Nallathambi, Subbaiah Ramasamy Krishnadas, Perumalsamy Vijayalakshmi, Shetty Shashikanth, Jon Martin Collinson, Periasamy Sundaresan*

*Corresponding author for this work

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Background: Haploinsufficiency at the PAX6 locus causes aniridia, a panocular eye condition characterized by iris hypoplasia and a variety of other anterior and posterior eye defects leading to poor vision. This study was performed to identify novel PAX6 mutations that lead to familial aniridia in Indian patients. Methods: Genomic DNA was isolated from affected individuals (clinically diagnosed aniridia) from nine unrelated aniridic pedigrees, unaffected family members, and unrelated normal controls. The coding regions of PAX6 were amplified and subjected to single strand conformation polymorphism (SSCP) gel analysis, and direct cloning and sequencing. Results: SSCP band shifts, indicative of DNA base pair mutations, were observed in five of these unrelated families. Four mutations were shown to be previously unreported insertion or deletions in PAX6, leading to frameshifts. These new mutations were c.1174delTG (in exon 10), c.710delC (exon 6), c.406delTT (exon 5) and c.393insTCAGC (exon 5). The other nonsense mutation, a transition (c.1080C>T) in exon 9, has been reported previously as a mutation hotspot for PAX6 in other ethnic pedigrees. All mutant alleles transmitted through aniridic individuals in each family. Conclusion: These new deletions and an insertion create frameshifts, which are predicted to introduce premature termination codons into the PAX6 reading frame. The genetic alterations carried by affected individuals are predicted to lead to loss-of-function mutations that would segregate in an autosomal dominant manner to subsequent generations. This is the first report of the 'hotspot' c.1080C>T transition from Indian families.

Original languageEnglish
Article number28
JournalBMC Ophthalmology
Volume6
DOIs
Publication statusPublished - 27 Jun 2006

ASJC Scopus subject areas

  • Ophthalmology

Fingerprint Dive into the research topics of 'Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia'. Together they form a unique fingerprint.

  • Cite this

    Neethirajan, G., Nallathambi, J., Krishnadas, S. R., Vijayalakshmi, P., Shashikanth, S., Collinson, J. M., & Sundaresan, P. (2006). Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia. BMC Ophthalmology, 6, [28]. https://doi.org/10.1186/1471-2415-6-28