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Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India
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. To elucidate the possible role of SNCA gene in the pathoge...
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Published in: | Neurology India 2014-03, Vol.62 (2), p.149-152 |
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creator | Kadakol, G S Kulkarni, S S Wali, G M Gai, Pramod B |
description | 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.
To elucidate the possible role of SNCA gene in the pathogenesis of PD in Indian population specifically in north Karnataka.
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.
No mutations were observed in SNCA gene of PD samples in comparison with control samples.
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. |
doi_str_mv | 10.4103/0028-3886.132338 |
format | article |
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To elucidate the possible role of SNCA gene in the pathogenesis of PD in Indian population specifically in north Karnataka.
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.
No mutations were observed in SNCA gene of PD samples in comparison with control samples.
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.</description><identifier>ISSN: 0028-3886</identifier><identifier>DOI: 10.4103/0028-3886.132338</identifier><identifier>PMID: 24823723</identifier><language>eng</language><publisher>India</publisher><subject>Adult ; alpha-Synuclein - genetics ; DNA Mutational Analysis - methods ; Gene Expression Regulation ; Genetic Predisposition to Disease ; Humans ; India ; Male ; Middle Aged ; Mutation - genetics ; Parkinson Disease - diagnosis ; Parkinson Disease - genetics</subject><ispartof>Neurology India, 2014-03, Vol.62 (2), p.149-152</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,37013</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24823723$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kadakol, G S</creatorcontrib><creatorcontrib>Kulkarni, S S</creatorcontrib><creatorcontrib>Wali, G M</creatorcontrib><creatorcontrib>Gai, Pramod B</creatorcontrib><title>Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India</title><title>Neurology India</title><addtitle>Neurol India</addtitle><description>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.
To elucidate the possible role of SNCA gene in the pathogenesis of PD in Indian population specifically in north Karnataka.
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.
No mutations were observed in SNCA gene of PD samples in comparison with control samples.
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.</description><subject>Adult</subject><subject>alpha-Synuclein - genetics</subject><subject>DNA Mutational Analysis - methods</subject><subject>Gene Expression Regulation</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>India</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation - genetics</subject><subject>Parkinson Disease - diagnosis</subject><subject>Parkinson Disease - genetics</subject><issn>0028-3886</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNo9kD1PwzAYhD2AaCnsTMgbDKTYfp3EGVHFR0X5GEBii94kNpi6TrGToT-LP8JvIoLCdLrTo5PuCDnibCo5g3PGhEpAqWzKQQCoHTL-j0ZkP8b3wQJwsUdGQioBuYAxeblrna57h4GiR7eJNtLW0K_PJG58XzttPX3VXtNBHzEsrY-tP4m0sVFj_Inv29C90VsMHjtc4hmd-8biAdk16KI-3OqEPF9dPs1uksXD9Xx2sUjWgvMuMWg0r7FKoQCd86KRIAQ0QuRFJbkyNajcMKhZnmaVlJgZBaopRKEUZKxIYUJOf3vXof3odezKlY21dg69bvtY8nQYy5UENqDHW7SvVrop18GuMGzKvzfgG6vEXsY</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Kadakol, G S</creator><creator>Kulkarni, S S</creator><creator>Wali, G M</creator><creator>Gai, Pramod B</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20140301</creationdate><title>Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India</title><author>Kadakol, G S ; Kulkarni, S S ; Wali, G M ; Gai, Pramod B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-fafe1cab5393e719d43223d2279b418fc387f03c0756b44a6f838d92988360953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>alpha-Synuclein - genetics</topic><topic>DNA Mutational Analysis - methods</topic><topic>Gene Expression Regulation</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>India</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation - genetics</topic><topic>Parkinson Disease - diagnosis</topic><topic>Parkinson Disease - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kadakol, G S</creatorcontrib><creatorcontrib>Kulkarni, S S</creatorcontrib><creatorcontrib>Wali, G M</creatorcontrib><creatorcontrib>Gai, Pramod B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Neurology India</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kadakol, G S</au><au>Kulkarni, S S</au><au>Wali, G M</au><au>Gai, Pramod B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India</atitle><jtitle>Neurology India</jtitle><addtitle>Neurol India</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>62</volume><issue>2</issue><spage>149</spage><epage>152</epage><pages>149-152</pages><issn>0028-3886</issn><abstract>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.
To elucidate the possible role of SNCA gene in the pathogenesis of PD in Indian population specifically in north Karnataka.
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.
No mutations were observed in SNCA gene of PD samples in comparison with control samples.
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.</abstract><cop>India</cop><pmid>24823723</pmid><doi>10.4103/0028-3886.132338</doi><tpages>4</tpages></addata></record> |
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subjects | Adult alpha-Synuclein - genetics DNA Mutational Analysis - methods Gene Expression Regulation Genetic Predisposition to Disease Humans India Male Middle Aged Mutation - genetics Parkinson Disease - diagnosis Parkinson Disease - genetics |
title | Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India |
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