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Cloning and Complete Nucleotide Sequence of a Full-Length cDNA Encoding a Catalytically Functional Tumor-Associated Aldehyde Dehydrogenase
To study the mechanism(s) controlling expression of the tumor-associated aldehyde dehydrogenase (tumor ALDH), which appears during rat hepatocarcinogenesis, cDNAs encoding this isozyme were cloned and identified with an antibody probe. Poly(A)-containing RNA from HTC rat hepatoma cells, which have b...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1988-03, Vol.85 (6), p.1782-1786 |
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description | To study the mechanism(s) controlling expression of the tumor-associated aldehyde dehydrogenase (tumor ALDH), which appears during rat hepatocarcinogenesis, cDNAs encoding this isozyme were cloned and identified with an antibody probe. Poly(A)-containing RNA from HTC rat hepatoma cells, which have been shown to possess high levels of tumor ALDH, was used as template to synthesize double-stranded cDNA. The cDNA was methylated to protect internal sites. Two different synthetic DNA linkers were added sequentially to the cDNA to insure correct orientation for expression from the lac promoter of pUC8. A library of 100,000 independent members carrying inserts >1 kilobase was obtained. From this library, two apparently identical tumor ALDH clones, differing only in size, were identified with an indirect immunological probe. The larger of the cDNA clones identified, pTALDH, was chosen for further study. Interestingly, since tumor ALDH is a dimeric enzyme, pTALDH directs synthesis of a functional tumor ALDH in the bacterial cell. The cDNA sequence has been confirmed by comparison to the amino acid sequence of tumor ALDH purified from HTC cells. |
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Poly(A)-containing RNA from HTC rat hepatoma cells, which have been shown to possess high levels of tumor ALDH, was used as template to synthesize double-stranded cDNA. The cDNA was methylated to protect internal sites. Two different synthetic DNA linkers were added sequentially to the cDNA to insure correct orientation for expression from the lac promoter of pUC8. A library of 100,000 independent members carrying inserts >1 kilobase was obtained. From this library, two apparently identical tumor ALDH clones, differing only in size, were identified with an indirect immunological probe. The larger of the cDNA clones identified, pTALDH, was chosen for further study. Interestingly, since tumor ALDH is a dimeric enzyme, pTALDH directs synthesis of a functional tumor ALDH in the bacterial cell. The cDNA sequence has been confirmed by comparison to the amino acid sequence of tumor ALDH purified from HTC cells.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.85.6.1782</identifier><identifier>PMID: 2831537</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Aldehyde Dehydrogenase - genetics ; Aldehydes ; Amino Acid Sequence ; Amino acids ; Animals ; Base Sequence ; Biological and medical sciences ; Biotechnology ; Cloning, Molecular ; Complementary DNA ; Deoxyribonucleases, Type II Site-Specific ; DNA - analysis ; DNA Restriction Enzymes - metabolism ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Gels ; Genetic engineering ; Genetic technics ; Liver ; Liver Neoplasms, Experimental - enzymology ; Methods. Procedures. Technologies ; Molecular Sequence Data ; Nucleotides ; Phenotype ; Rats ; RNA ; Tumors</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1988-03, Vol.85 (6), p.1782-1786</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-36087c021577073c0598b49c96d0fc91b403565dc8707d48883bd6b804d24b3e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/85/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/31389$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/31389$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,58219,58452</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7094606$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2831537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jones, David E.</creatorcontrib><creatorcontrib>Brennan, Mark D.</creatorcontrib><creatorcontrib>Hempel, John</creatorcontrib><creatorcontrib>Lindahl, Ronald</creatorcontrib><title>Cloning and Complete Nucleotide Sequence of a Full-Length cDNA Encoding a Catalytically Functional Tumor-Associated Aldehyde Dehydrogenase</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>To study the mechanism(s) controlling expression of the tumor-associated aldehyde dehydrogenase (tumor ALDH), which appears during rat hepatocarcinogenesis, cDNAs encoding this isozyme were cloned and identified with an antibody probe. Poly(A)-containing RNA from HTC rat hepatoma cells, which have been shown to possess high levels of tumor ALDH, was used as template to synthesize double-stranded cDNA. The cDNA was methylated to protect internal sites. Two different synthetic DNA linkers were added sequentially to the cDNA to insure correct orientation for expression from the lac promoter of pUC8. A library of 100,000 independent members carrying inserts >1 kilobase was obtained. From this library, two apparently identical tumor ALDH clones, differing only in size, were identified with an indirect immunological probe. The larger of the cDNA clones identified, pTALDH, was chosen for further study. Interestingly, since tumor ALDH is a dimeric enzyme, pTALDH directs synthesis of a functional tumor ALDH in the bacterial cell. The cDNA sequence has been confirmed by comparison to the amino acid sequence of tumor ALDH purified from HTC cells.</description><subject>Aldehyde Dehydrogenase - genetics</subject><subject>Aldehydes</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cloning, Molecular</subject><subject>Complementary DNA</subject><subject>Deoxyribonucleases, Type II Site-Specific</subject><subject>DNA - analysis</subject><subject>DNA Restriction Enzymes - metabolism</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Liver</subject><subject>Liver Neoplasms, Experimental - enzymology</subject><subject>Methods. Procedures. Technologies</subject><subject>Molecular Sequence Data</subject><subject>Nucleotides</subject><subject>Phenotype</subject><subject>Rats</subject><subject>RNA</subject><subject>Tumors</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhS0EKkNhywIJyQvELsGO7dhejtIWkEZlQVlbju1MU3nsIXakzivw1DjMMOoCidVdnO-e-3MAeItRjREnn_ZBp1qwuq0xF80zsMJI4qqlEj0HK4QaXgna0JfgVUoPCCHJBLoAF40gmBG-Ar86H8MYtlAHC7u423uXHbydjXcxj9bB7-7n7IJxMA5Qw5vZ-2rjwjbfQ3N1u4bXwUT7px92Omt_yKPR3h8KGUweY9Ae3s27OFXrlKIZdXYWrr1194difrWUKW5dOcK9Bi8G7ZN7c6qX4MfN9V33pdp8-_y1W28qwxqRK9IiwQ1qMOO8PMAgJkVPpZGtRYORuKeIsJZZI4psqRCC9LbtBaK2oT1x5BJ8PPrup1huS1ntxmSc9zq4OCfFBW4Eo_y_IKaSliGogPURNFNMaXKD2k_jTk8HhZFaUlJLSkow1aolpdLw_uQ89ztnz_gplqJ_OOk6lXcOkw5mTGeMI0lb1D5ZcLH_q57HqKGkld1jfjLvn2DR3x31h5TjdAYIJkKS3-JguuI</recordid><startdate>19880301</startdate><enddate>19880301</enddate><creator>Jones, David E.</creator><creator>Brennan, Mark D.</creator><creator>Hempel, John</creator><creator>Lindahl, Ronald</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>IQODW</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19880301</creationdate><title>Cloning and Complete Nucleotide Sequence of a Full-Length cDNA Encoding a Catalytically Functional Tumor-Associated Aldehyde Dehydrogenase</title><author>Jones, David E. ; Brennan, Mark D. ; Hempel, John ; Lindahl, Ronald</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-36087c021577073c0598b49c96d0fc91b403565dc8707d48883bd6b804d24b3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Aldehyde Dehydrogenase - genetics</topic><topic>Aldehydes</topic><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cloning, Molecular</topic><topic>Complementary DNA</topic><topic>Deoxyribonucleases, Type II Site-Specific</topic><topic>DNA - analysis</topic><topic>DNA Restriction Enzymes - metabolism</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Liver</topic><topic>Liver Neoplasms, Experimental - enzymology</topic><topic>Methods. Procedures. Technologies</topic><topic>Molecular Sequence Data</topic><topic>Nucleotides</topic><topic>Phenotype</topic><topic>Rats</topic><topic>RNA</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jones, David E.</creatorcontrib><creatorcontrib>Brennan, Mark D.</creatorcontrib><creatorcontrib>Hempel, John</creatorcontrib><creatorcontrib>Lindahl, Ronald</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, David E.</au><au>Brennan, Mark D.</au><au>Hempel, John</au><au>Lindahl, Ronald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning and Complete Nucleotide Sequence of a Full-Length cDNA Encoding a Catalytically Functional Tumor-Associated Aldehyde Dehydrogenase</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1988-03-01</date><risdate>1988</risdate><volume>85</volume><issue>6</issue><spage>1782</spage><epage>1786</epage><pages>1782-1786</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>To study the mechanism(s) controlling expression of the tumor-associated aldehyde dehydrogenase (tumor ALDH), which appears during rat hepatocarcinogenesis, cDNAs encoding this isozyme were cloned and identified with an antibody probe. Poly(A)-containing RNA from HTC rat hepatoma cells, which have been shown to possess high levels of tumor ALDH, was used as template to synthesize double-stranded cDNA. The cDNA was methylated to protect internal sites. Two different synthetic DNA linkers were added sequentially to the cDNA to insure correct orientation for expression from the lac promoter of pUC8. A library of 100,000 independent members carrying inserts >1 kilobase was obtained. From this library, two apparently identical tumor ALDH clones, differing only in size, were identified with an indirect immunological probe. The larger of the cDNA clones identified, pTALDH, was chosen for further study. Interestingly, since tumor ALDH is a dimeric enzyme, pTALDH directs synthesis of a functional tumor ALDH in the bacterial cell. The cDNA sequence has been confirmed by comparison to the amino acid sequence of tumor ALDH purified from HTC cells.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>2831537</pmid><doi>10.1073/pnas.85.6.1782</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aldehyde Dehydrogenase - genetics Aldehydes Amino Acid Sequence Amino acids Animals Base Sequence Biological and medical sciences Biotechnology Cloning, Molecular Complementary DNA Deoxyribonucleases, Type II Site-Specific DNA - analysis DNA Restriction Enzymes - metabolism Enzymes Fundamental and applied biological sciences. Psychology Gels Genetic engineering Genetic technics Liver Liver Neoplasms, Experimental - enzymology Methods. Procedures. Technologies Molecular Sequence Data Nucleotides Phenotype Rats RNA Tumors |
title | Cloning and Complete Nucleotide Sequence of a Full-Length cDNA Encoding a Catalytically Functional Tumor-Associated Aldehyde Dehydrogenase |
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