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Analysis of four novel variants of Nav1.5/SCN5A cloned from the brain
Na + currents with tetrodotoxin resistance (TTX-R) have been observed in neurons, but the full-length cDNAs encoding the TTX-R Nav1.5 channels in human and rat brains have not been identified. In this study, four full-length cDNAs encoding the α-subunits of the Nav1.5 channels in human and rat cereb...
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Published in: | Neuroscience research 2009-08, Vol.64 (4), p.339-347 |
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description | Na
+ currents with tetrodotoxin resistance (TTX-R) have been observed in neurons, but the full-length cDNAs encoding the TTX-R Nav1.5 channels in human and rat brains have not been identified. In this study, four full-length cDNAs encoding the α-subunits of the Nav1.5 channels in human and rat cerebral cortexes were cloned and designated hB1, hB2, rN1 and rN2 (accession number:
EF629346,
EF629347,
EF618549,
EF618550). The longest open reading frame of hB1 or rN1 encodes 2016 amino acid residues. Sequence analysis has indicated that hB1 is highly homologus with human cardiac Nav1.5/SCN5A (hH1) with >98% amino acid identity. Genomic sequence analysis of Nav1.5/SCN5A revealed that it is exon6A rather than exon6 splice variant of Nav1.5 which is expressed in human and rat brains. Alternative splicing variants hB2 and rN2, which lack exon24 and encode proteins of 1998 amino acids, were also identified. Furthermore, the total Nav1.5 mRNA and Navβ1 mRNA were detected in 16 different tissue types of developing Wistar rats by reverse polymerase chain reaction (RT-PCR), and their expression patterns varied among different tissue types with age development. These results suggest that Nav1.5 channels in human and rat brains are encoded by new variants of Nav1.5/SCN5A and Nav1.5 is more widely distributed and expressed than previously thought. |
doi_str_mv | 10.1016/j.neures.2009.04.003 |
format | article |
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+ currents with tetrodotoxin resistance (TTX-R) have been observed in neurons, but the full-length cDNAs encoding the TTX-R Nav1.5 channels in human and rat brains have not been identified. In this study, four full-length cDNAs encoding the α-subunits of the Nav1.5 channels in human and rat cerebral cortexes were cloned and designated hB1, hB2, rN1 and rN2 (accession number:
EF629346,
EF629347,
EF618549,
EF618550). The longest open reading frame of hB1 or rN1 encodes 2016 amino acid residues. Sequence analysis has indicated that hB1 is highly homologus with human cardiac Nav1.5/SCN5A (hH1) with >98% amino acid identity. Genomic sequence analysis of Nav1.5/SCN5A revealed that it is exon6A rather than exon6 splice variant of Nav1.5 which is expressed in human and rat brains. Alternative splicing variants hB2 and rN2, which lack exon24 and encode proteins of 1998 amino acids, were also identified. Furthermore, the total Nav1.5 mRNA and Navβ1 mRNA were detected in 16 different tissue types of developing Wistar rats by reverse polymerase chain reaction (RT-PCR), and their expression patterns varied among different tissue types with age development. These results suggest that Nav1.5 channels in human and rat brains are encoded by new variants of Nav1.5/SCN5A and Nav1.5 is more widely distributed and expressed than previously thought.</description><identifier>ISSN: 0168-0102</identifier><identifier>EISSN: 1872-8111</identifier><identifier>DOI: 10.1016/j.neures.2009.04.003</identifier><identifier>PMID: 19376164</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Aging - genetics ; Aging - metabolism ; Alternative splicing ; Alternative Splicing - genetics ; Animals ; Animals, Newborn ; Brain - metabolism ; Cloning, Molecular - methods ; DNA, Complementary - analysis ; DNA, Complementary - genetics ; Exons - genetics ; Expression ; Full-length cDNA ; Human brain ; Humans ; Male ; Molecular Sequence Data ; Muscle Proteins - chemistry ; Muscle Proteins - genetics ; NAV1.5 Voltage-Gated Sodium Channel ; Nav1.5/SCN5A ; Open Reading Frames - genetics ; Protein Isoforms - chemistry ; Protein Isoforms - genetics ; Protein Subunits - chemistry ; Protein Subunits - genetics ; Rat brain ; Rats ; Rats, Wistar ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - analysis ; RNA, Messenger - genetics ; Sequence Homology, Amino Acid ; Sequence Homology, Nucleic Acid ; Sodium Channels - chemistry ; Sodium Channels - genetics ; Species Specificity ; Variants</subject><ispartof>Neuroscience research, 2009-08, Vol.64 (4), p.339-347</ispartof><rights>2009 Elsevier Ireland Ltd and the Japan Neuroscience Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-e1895431912ef3a2c3aab95b4e61e6c8b74b99e4b7495c0cd27f40f7367a41083</citedby><cites>FETCH-LOGICAL-c416t-e1895431912ef3a2c3aab95b4e61e6c8b74b99e4b7495c0cd27f40f7367a41083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168010209001199$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45779</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19376164$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Jun</creatorcontrib><creatorcontrib>Ou, Shao-Wu</creatorcontrib><creatorcontrib>Wang, Yun-Jie</creatorcontrib><creatorcontrib>Kameyama, Masaki</creatorcontrib><creatorcontrib>Kameyama, Asako</creatorcontrib><creatorcontrib>Zong, Zhi-Hong</creatorcontrib><title>Analysis of four novel variants of Nav1.5/SCN5A cloned from the brain</title><title>Neuroscience research</title><addtitle>Neurosci Res</addtitle><description>Na
+ currents with tetrodotoxin resistance (TTX-R) have been observed in neurons, but the full-length cDNAs encoding the TTX-R Nav1.5 channels in human and rat brains have not been identified. In this study, four full-length cDNAs encoding the α-subunits of the Nav1.5 channels in human and rat cerebral cortexes were cloned and designated hB1, hB2, rN1 and rN2 (accession number:
EF629346,
EF629347,
EF618549,
EF618550). The longest open reading frame of hB1 or rN1 encodes 2016 amino acid residues. Sequence analysis has indicated that hB1 is highly homologus with human cardiac Nav1.5/SCN5A (hH1) with >98% amino acid identity. Genomic sequence analysis of Nav1.5/SCN5A revealed that it is exon6A rather than exon6 splice variant of Nav1.5 which is expressed in human and rat brains. Alternative splicing variants hB2 and rN2, which lack exon24 and encode proteins of 1998 amino acids, were also identified. Furthermore, the total Nav1.5 mRNA and Navβ1 mRNA were detected in 16 different tissue types of developing Wistar rats by reverse polymerase chain reaction (RT-PCR), and their expression patterns varied among different tissue types with age development. These results suggest that Nav1.5 channels in human and rat brains are encoded by new variants of Nav1.5/SCN5A and Nav1.5 is more widely distributed and expressed than previously thought.</description><subject>Aging - genetics</subject><subject>Aging - metabolism</subject><subject>Alternative splicing</subject><subject>Alternative Splicing - genetics</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Brain - metabolism</subject><subject>Cloning, Molecular - methods</subject><subject>DNA, Complementary - analysis</subject><subject>DNA, Complementary - genetics</subject><subject>Exons - genetics</subject><subject>Expression</subject><subject>Full-length cDNA</subject><subject>Human brain</subject><subject>Humans</subject><subject>Male</subject><subject>Molecular Sequence Data</subject><subject>Muscle Proteins - chemistry</subject><subject>Muscle Proteins - genetics</subject><subject>NAV1.5 Voltage-Gated Sodium Channel</subject><subject>Nav1.5/SCN5A</subject><subject>Open Reading Frames - genetics</subject><subject>Protein Isoforms - chemistry</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Subunits - chemistry</subject><subject>Protein Subunits - genetics</subject><subject>Rat brain</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - genetics</subject><subject>Sequence Homology, Amino Acid</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Sodium Channels - chemistry</subject><subject>Sodium Channels - genetics</subject><subject>Species Specificity</subject><subject>Variants</subject><issn>0168-0102</issn><issn>1872-8111</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLAzEUhYMotj7-gcisdDVjbpJ5ZCOUUh9QdKGuQyZzB1Omk5rMFPrvjbbgztWBy3fOhY-QK6AZUCjuVlmPo8eQMUplRkVGKT8iU6hKllYAcEymEatSCpRNyFkIKxoJKfgpmYDkZQGFmJLFrNfdLtiQuDZp3eiT3m2xS7baW90Pv-cXvYUsv3ubv-SzxHSuxyZpvVsnwycmtde2vyAnre4CXh7ynHw8LN7nT-ny9fF5PlumRkAxpAiVzAUHCQxbrpnhWtcyrwUWgIWp6lLUUqKIKXNDTcPKVtC25EWpBdCKn5Pb_e7Gu68Rw6DWNhjsOt2jG4MqOWdMsEJE8uZfMkorc1qxCIo9aLwLwWOrNt6utd8poOpHtFqpveifjlRUqKgx1q4P-2O9xuavdDAbgfs9gNHH1qJXwVjsDTbWoxlU4-z_H74Blu-OPA</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Wang, Jun</creator><creator>Ou, Shao-Wu</creator><creator>Wang, Yun-Jie</creator><creator>Kameyama, Masaki</creator><creator>Kameyama, Asako</creator><creator>Zong, Zhi-Hong</creator><general>Elsevier Ireland Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20090801</creationdate><title>Analysis of four novel variants of Nav1.5/SCN5A cloned from the brain</title><author>Wang, Jun ; Ou, Shao-Wu ; Wang, Yun-Jie ; Kameyama, Masaki ; Kameyama, Asako ; Zong, Zhi-Hong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-e1895431912ef3a2c3aab95b4e61e6c8b74b99e4b7495c0cd27f40f7367a41083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aging - genetics</topic><topic>Aging - metabolism</topic><topic>Alternative splicing</topic><topic>Alternative Splicing - genetics</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Brain - metabolism</topic><topic>Cloning, Molecular - methods</topic><topic>DNA, Complementary - analysis</topic><topic>DNA, Complementary - genetics</topic><topic>Exons - genetics</topic><topic>Expression</topic><topic>Full-length cDNA</topic><topic>Human brain</topic><topic>Humans</topic><topic>Male</topic><topic>Molecular Sequence Data</topic><topic>Muscle Proteins - chemistry</topic><topic>Muscle Proteins - genetics</topic><topic>NAV1.5 Voltage-Gated Sodium Channel</topic><topic>Nav1.5/SCN5A</topic><topic>Open Reading Frames - genetics</topic><topic>Protein Isoforms - chemistry</topic><topic>Protein Isoforms - genetics</topic><topic>Protein Subunits - chemistry</topic><topic>Protein Subunits - genetics</topic><topic>Rat brain</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - genetics</topic><topic>Sequence Homology, Amino Acid</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Sodium Channels - chemistry</topic><topic>Sodium Channels - genetics</topic><topic>Species Specificity</topic><topic>Variants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Jun</creatorcontrib><creatorcontrib>Ou, Shao-Wu</creatorcontrib><creatorcontrib>Wang, Yun-Jie</creatorcontrib><creatorcontrib>Kameyama, Masaki</creatorcontrib><creatorcontrib>Kameyama, Asako</creatorcontrib><creatorcontrib>Zong, Zhi-Hong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Jun</au><au>Ou, Shao-Wu</au><au>Wang, Yun-Jie</au><au>Kameyama, Masaki</au><au>Kameyama, Asako</au><au>Zong, Zhi-Hong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of four novel variants of Nav1.5/SCN5A cloned from the brain</atitle><jtitle>Neuroscience research</jtitle><addtitle>Neurosci Res</addtitle><date>2009-08-01</date><risdate>2009</risdate><volume>64</volume><issue>4</issue><spage>339</spage><epage>347</epage><pages>339-347</pages><issn>0168-0102</issn><eissn>1872-8111</eissn><abstract>Na
+ currents with tetrodotoxin resistance (TTX-R) have been observed in neurons, but the full-length cDNAs encoding the TTX-R Nav1.5 channels in human and rat brains have not been identified. In this study, four full-length cDNAs encoding the α-subunits of the Nav1.5 channels in human and rat cerebral cortexes were cloned and designated hB1, hB2, rN1 and rN2 (accession number:
EF629346,
EF629347,
EF618549,
EF618550). The longest open reading frame of hB1 or rN1 encodes 2016 amino acid residues. Sequence analysis has indicated that hB1 is highly homologus with human cardiac Nav1.5/SCN5A (hH1) with >98% amino acid identity. Genomic sequence analysis of Nav1.5/SCN5A revealed that it is exon6A rather than exon6 splice variant of Nav1.5 which is expressed in human and rat brains. Alternative splicing variants hB2 and rN2, which lack exon24 and encode proteins of 1998 amino acids, were also identified. Furthermore, the total Nav1.5 mRNA and Navβ1 mRNA were detected in 16 different tissue types of developing Wistar rats by reverse polymerase chain reaction (RT-PCR), and their expression patterns varied among different tissue types with age development. These results suggest that Nav1.5 channels in human and rat brains are encoded by new variants of Nav1.5/SCN5A and Nav1.5 is more widely distributed and expressed than previously thought.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>19376164</pmid><doi>10.1016/j.neures.2009.04.003</doi><tpages>9</tpages></addata></record> |
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subjects | Aging - genetics Aging - metabolism Alternative splicing Alternative Splicing - genetics Animals Animals, Newborn Brain - metabolism Cloning, Molecular - methods DNA, Complementary - analysis DNA, Complementary - genetics Exons - genetics Expression Full-length cDNA Human brain Humans Male Molecular Sequence Data Muscle Proteins - chemistry Muscle Proteins - genetics NAV1.5 Voltage-Gated Sodium Channel Nav1.5/SCN5A Open Reading Frames - genetics Protein Isoforms - chemistry Protein Isoforms - genetics Protein Subunits - chemistry Protein Subunits - genetics Rat brain Rats Rats, Wistar Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - analysis RNA, Messenger - genetics Sequence Homology, Amino Acid Sequence Homology, Nucleic Acid Sodium Channels - chemistry Sodium Channels - genetics Species Specificity Variants |
title | Analysis of four novel variants of Nav1.5/SCN5A cloned from the brain |
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