ORIGINAL ARTICLE |
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Year : 2014 | Volume
: 62
| Issue : 2 | Page : 149--152 |
Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India
G. S. Kadakol1, S. S. Kulkarni2, G. M. Wali3, Pramod B. Gai2
1 Department of Applied Genetics, Karnatak University, Dharwad, Karnataka, India 2 Karntaka Institute for DNA Research, Pavate Nagar, Dharwad, Karnataka, India 3 Neurospeciality Centre, Belgaum, Karnataka, India
Correspondence Address:
Pramod B. Gai Director, Karntaka Institute for DNA Research, Pavate Nagar, Dharwad - 580 003, Karnataka India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0028-3886.132338
Background: Parkinson's disease (PD) is a disabling neurological disorder characterized by progressive degeneration of dopaminergic neurons. Mutations analysis within the α-synuclein gene (SNCA) on chromosome 4 has been reported in the last decade. Objective: To elucidate the possible role of SNCA gene in the pathogenesis of PD in Indian population specifically in north Karnataka. Materials and Methods: The study subjects included 100 clinically diagnosed PD patients and 100 ethnically matched healthy controls. Isolated deoxyribonucleic acid (DNA) samples from both were subjected to exon-specific polymerase chain reaction (PCR) amplification and amplicons were subjected to capillary-based direct DNA sequencing. Result: No mutations were observed in SNCA gene of PD samples in comparison with control samples. Conclusion: These findings support the hypothesis that the SNCA gene mutations might be population specific and may not be playing role in causing PD in all the populations.
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