The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing
The alpha1C subunit is the pore-forming protein for the L-type calcium channel. Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a s...
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Veröffentlicht in: | Molecular and cellular biochemistry 2005-01, Vol.269 (1-2), p.153-163 |
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description | The alpha1C subunit is the pore-forming protein for the L-type calcium channel. Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a single piece (6.64 kb). Using 75 positive clones that were identified by restriction enzyme mapping, we tested the alternative splicing patterns of the Ca(v) 1.2 gene that encodes the alpha1C subunit protein and focused on five loci: IS6, post-IS6, IIIS2, IVS3, and the c-terminus. The results indicate that: (1) alternative splicing occurs in most of the loci, giving rise to two or three different isoforms at those sites; (2) there is a predominant form for each splicing site, (3) there does not appear to be consistent coordination of splicing at multiple loci of this gene. Alternative splicing is not tissue-specific in most regions. |
doi_str_mv | 10.1007/s11010-005-3455-8 |
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Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a single piece (6.64 kb). Using 75 positive clones that were identified by restriction enzyme mapping, we tested the alternative splicing patterns of the Ca(v) 1.2 gene that encodes the alpha1C subunit protein and focused on five loci: IS6, post-IS6, IIIS2, IVS3, and the c-terminus. The results indicate that: (1) alternative splicing occurs in most of the loci, giving rise to two or three different isoforms at those sites; (2) there is a predominant form for each splicing site, (3) there does not appear to be consistent coordination of splicing at multiple loci of this gene. Alternative splicing is not tissue-specific in most regions.</description><identifier>ISSN: 0300-8177</identifier><identifier>EISSN: 1573-4919</identifier><identifier>DOI: 10.1007/s11010-005-3455-8</identifier><identifier>PMID: 15786728</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Alternative Splicing ; Animals ; Calcium channels ; Calcium Channels, L-Type - genetics ; Cloning, Molecular ; Gene expression ; Male ; Myocytes, Cardiac - metabolism ; Protein Isoforms - genetics ; Protein Structure, Tertiary ; Proteins ; Rats ; Rats, Sprague-Dawley ; Restriction Mapping ; RNA Splice Sites ; RNA, Messenger - metabolism ; Tissue Distribution</subject><ispartof>Molecular and cellular biochemistry, 2005-01, Vol.269 (1-2), p.153-163</ispartof><rights>Springer Science + Business Media, Inc. 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-be59b8a39d034690d5873b868da91d242bf30096538b092070f90841152e628b3</citedby><cites>FETCH-LOGICAL-c421t-be59b8a39d034690d5873b868da91d242bf30096538b092070f90841152e628b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15786728$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fan, Q Ivy</creatorcontrib><creatorcontrib>Vanderpool, Kathleen M</creatorcontrib><creatorcontrib>Chung, Hui-San</creatorcontrib><creatorcontrib>Marsh, James D</creatorcontrib><title>The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing</title><title>Molecular and cellular biochemistry</title><addtitle>Mol Cell Biochem</addtitle><description>The alpha1C subunit is the pore-forming protein for the L-type calcium channel. Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a single piece (6.64 kb). Using 75 positive clones that were identified by restriction enzyme mapping, we tested the alternative splicing patterns of the Ca(v) 1.2 gene that encodes the alpha1C subunit protein and focused on five loci: IS6, post-IS6, IIIS2, IVS3, and the c-terminus. The results indicate that: (1) alternative splicing occurs in most of the loci, giving rise to two or three different isoforms at those sites; (2) there is a predominant form for each splicing site, (3) there does not appear to be consistent coordination of splicing at multiple loci of this gene. Alternative splicing is not tissue-specific in most regions.</description><subject>Alternative Splicing</subject><subject>Animals</subject><subject>Calcium channels</subject><subject>Calcium Channels, L-Type - genetics</subject><subject>Cloning, Molecular</subject><subject>Gene expression</subject><subject>Male</subject><subject>Myocytes, Cardiac - metabolism</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Structure, Tertiary</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Restriction Mapping</subject><subject>RNA Splice Sites</subject><subject>RNA, Messenger - metabolism</subject><subject>Tissue Distribution</subject><issn>0300-8177</issn><issn>1573-4919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0k2LFDEQBuAgijuu_gAvEjzoxWhVvnOUwS8Y8LKeQ7q7ZqaXnnTb6Rb335tlBgQP7ikheaqgkpexlwjvEcB9KIiAIACMUNoY4R-xDRqnhA4YHrMNKADh0bkr9qyUW6gYEJ-yq4q8ddJv2PHmSHwnlruJeJuGtl9PvD2mnGngaZiOieOWl7VZc7_wA2Xia-5oPoxUOP1eKJf-F72rh-04zl2f00JdLVxortt6xcs09G2fD8_Zk30aCr24rNfsx-dPN9uvYvf9y7ftx51otcRFNGRC45MKHShtA3TGO9V467sUsJNaNvs6VLBG-QaCBAf7AF4jGklW-kZds7fnvtM8_lypLPHUl5aGIWUa1xKD9Wid1_JB6Y3STkurqnzzX2md0UqCfRCiU0ahhgpf_wNvx7U-2VCiM1ZqZZyrCM-oncdSZtrHae5Pab6LCPE-APEcgFgDEO8DEH2teXVpvDYn6v5WXH5c_QEh26kz</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Fan, Q Ivy</creator><creator>Vanderpool, Kathleen M</creator><creator>Chung, Hui-San</creator><creator>Marsh, James D</creator><general>Springer Nature B.V</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>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20050101</creationdate><title>The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing</title><author>Fan, Q Ivy ; Vanderpool, Kathleen M ; Chung, Hui-San ; Marsh, James D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-be59b8a39d034690d5873b868da91d242bf30096538b092070f90841152e628b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Alternative Splicing</topic><topic>Animals</topic><topic>Calcium channels</topic><topic>Calcium Channels, L-Type - genetics</topic><topic>Cloning, Molecular</topic><topic>Gene expression</topic><topic>Male</topic><topic>Myocytes, Cardiac - metabolism</topic><topic>Protein Isoforms - genetics</topic><topic>Protein Structure, Tertiary</topic><topic>Proteins</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Restriction Mapping</topic><topic>RNA Splice Sites</topic><topic>RNA, Messenger - metabolism</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fan, Q Ivy</creatorcontrib><creatorcontrib>Vanderpool, Kathleen M</creatorcontrib><creatorcontrib>Chung, Hui-San</creatorcontrib><creatorcontrib>Marsh, James D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fan, Q Ivy</au><au>Vanderpool, Kathleen M</au><au>Chung, Hui-San</au><au>Marsh, James D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing</atitle><jtitle>Molecular and cellular biochemistry</jtitle><addtitle>Mol Cell Biochem</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>269</volume><issue>1-2</issue><spage>153</spage><epage>163</epage><pages>153-163</pages><issn>0300-8177</issn><eissn>1573-4919</eissn><abstract>The alpha1C subunit is the pore-forming protein for the L-type calcium channel. Previous studies indicate that there is possible tissue-specific alternative splicing of this gene. In this study we cloned the entire open reading frame of the alpha1C subunit cDNA from adult rat cardiac myocytes in a single piece (6.64 kb). Using 75 positive clones that were identified by restriction enzyme mapping, we tested the alternative splicing patterns of the Ca(v) 1.2 gene that encodes the alpha1C subunit protein and focused on five loci: IS6, post-IS6, IIIS2, IVS3, and the c-terminus. The results indicate that: (1) alternative splicing occurs in most of the loci, giving rise to two or three different isoforms at those sites; (2) there is a predominant form for each splicing site, (3) there does not appear to be consistent coordination of splicing at multiple loci of this gene. Alternative splicing is not tissue-specific in most regions.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>15786728</pmid><doi>10.1007/s11010-005-3455-8</doi><tpages>11</tpages></addata></record> |
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subjects | Alternative Splicing Animals Calcium channels Calcium Channels, L-Type - genetics Cloning, Molecular Gene expression Male Myocytes, Cardiac - metabolism Protein Isoforms - genetics Protein Structure, Tertiary Proteins Rats Rats, Sprague-Dawley Restriction Mapping RNA Splice Sites RNA, Messenger - metabolism Tissue Distribution |
title | The L-type calcium channel alpha 1C subunit gene undergoes extensive, uncoordinated alternative splicing |
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