Isolation and sequence analysis of three cloned cDNAs for rabbit liver proteins that are related to rabbit cytochrome P-450 (form 2), the major phenobarbital-inducible form
We have isolated from rabbit liver three cDNA clones of 1400-1800 base pairs that hybridize selectively to RNA from animals treated with phenobarbital. The nucleotide sequences of the cDNAs have been determined. In the protein coding region the nucleotide sequences of two of the cDNAs are 88% homolo...
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Veröffentlicht in: | Biochemistry (Easton) 1984, Vol.23 (2), p.204-210 |
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description | We have isolated from rabbit liver three cDNA clones of 1400-1800 base pairs that hybridize selectively to RNA from animals treated with phenobarbital. The nucleotide sequences of the cDNAs have been determined. In the protein coding region the nucleotide sequences of two of the cDNAs are 88% homologous, and the third cDNA is about 72-74% homologous to the other two. All three are 55-60% homologous to rat liver cytochrome P-450b cDNA. The amino acid sequences derived from the cDNA sequences are about 50% homologous to those of rat liver cytochrome P-450b and rabbit liver cytochrome P-450 (form 2). The degree of homology differs substantially in different regions of the protein. The hydrophobicity profiles of these five mammalian cytochromes P-450 are very similar and contain up to eight regions of hydrophobicity that are long enough to span a membrane. These results indicate that these three cDNAs code for rabbit liver cytochromes P-450 which are different from any rabbit liver cytochrome P-450 for which amino acid sequence information is published. These cDNAs are part of a family of genes that are related to rabbit liver cytochrome P-450 (form 2) and rat liver cytochrome P-450b which are the major phenobarbital-inducible forms. The divergence of amino acid sequence between the rat and rabbit forms and the divergence of nucleotide sequences of silent sites in the two most closely related rabbit forms suggest that cytochromes P-450 have a relatively high rate of amino acid divergence compared to many other vertebrate proteins. |
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The nucleotide sequences of the cDNAs have been determined. In the protein coding region the nucleotide sequences of two of the cDNAs are 88% homologous, and the third cDNA is about 72-74% homologous to the other two. All three are 55-60% homologous to rat liver cytochrome P-450b cDNA. The amino acid sequences derived from the cDNA sequences are about 50% homologous to those of rat liver cytochrome P-450b and rabbit liver cytochrome P-450 (form 2). The degree of homology differs substantially in different regions of the protein. The hydrophobicity profiles of these five mammalian cytochromes P-450 are very similar and contain up to eight regions of hydrophobicity that are long enough to span a membrane. These results indicate that these three cDNAs code for rabbit liver cytochromes P-450 which are different from any rabbit liver cytochrome P-450 for which amino acid sequence information is published. These cDNAs are part of a family of genes that are related to rabbit liver cytochrome P-450 (form 2) and rat liver cytochrome P-450b which are the major phenobarbital-inducible forms. The divergence of amino acid sequence between the rat and rabbit forms and the divergence of nucleotide sequences of silent sites in the two most closely related rabbit forms suggest that cytochromes P-450 have a relatively high rate of amino acid divergence compared to many other vertebrate proteins.</description><identifier>ISSN: 0006-2960</identifier><identifier>EISSN: 1520-4995</identifier><identifier>DOI: 10.1021/bi00297a005</identifier><identifier>PMID: 6546520</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Biological and medical sciences ; Biotechnology ; Cloning, Molecular ; Codon - genetics ; cytochrome P-450 ; Cytochrome P-450 Enzyme System - genetics ; DNA - isolation & purification ; Enzyme Induction ; Fundamental and applied biological sciences. Psychology ; Genes ; Genetic engineering ; Genetic technics ; liver ; Liver - metabolism ; Male ; Methods. Procedures. Technologies ; Microsomes, Liver - drug effects ; Nucleic Acid Hybridization ; nucleotide sequence ; Phenobarbital - pharmacology ; Plasmids ; Rabbits</subject><ispartof>Biochemistry (Easton), 1984, Vol.23 (2), p.204-210</ispartof><rights>1984 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a329t-d0efaf112779f2872387e04870b283f5f0509ec7b5258a1f80ef24a4f43024bb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bi00297a005$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bi00297a005$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,4024,27076,27923,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9667873$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6546520$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leighton, John K</creatorcontrib><creatorcontrib>DeBrunner-Vossbrinck, Bettina A</creatorcontrib><creatorcontrib>Kemper, Byron</creatorcontrib><title>Isolation and sequence analysis of three cloned cDNAs for rabbit liver proteins that are related to rabbit cytochrome P-450 (form 2), the major phenobarbital-inducible form</title><title>Biochemistry (Easton)</title><addtitle>Biochemistry</addtitle><description>We have isolated from rabbit liver three cDNA clones of 1400-1800 base pairs that hybridize selectively to RNA from animals treated with phenobarbital. The nucleotide sequences of the cDNAs have been determined. In the protein coding region the nucleotide sequences of two of the cDNAs are 88% homologous, and the third cDNA is about 72-74% homologous to the other two. All three are 55-60% homologous to rat liver cytochrome P-450b cDNA. The amino acid sequences derived from the cDNA sequences are about 50% homologous to those of rat liver cytochrome P-450b and rabbit liver cytochrome P-450 (form 2). The degree of homology differs substantially in different regions of the protein. The hydrophobicity profiles of these five mammalian cytochromes P-450 are very similar and contain up to eight regions of hydrophobicity that are long enough to span a membrane. These results indicate that these three cDNAs code for rabbit liver cytochromes P-450 which are different from any rabbit liver cytochrome P-450 for which amino acid sequence information is published. These cDNAs are part of a family of genes that are related to rabbit liver cytochrome P-450 (form 2) and rat liver cytochrome P-450b which are the major phenobarbital-inducible forms. The divergence of amino acid sequence between the rat and rabbit forms and the divergence of nucleotide sequences of silent sites in the two most closely related rabbit forms suggest that cytochromes P-450 have a relatively high rate of amino acid divergence compared to many other vertebrate proteins.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cloning, Molecular</subject><subject>Codon - genetics</subject><subject>cytochrome P-450</subject><subject>Cytochrome P-450 Enzyme System - genetics</subject><subject>DNA - isolation & purification</subject><subject>Enzyme Induction</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>liver</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Methods. Procedures. Technologies</subject><subject>Microsomes, Liver - drug effects</subject><subject>Nucleic Acid Hybridization</subject><subject>nucleotide sequence</subject><subject>Phenobarbital - pharmacology</subject><subject>Plasmids</subject><subject>Rabbits</subject><issn>0006-2960</issn><issn>1520-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0k2P0zAQBuAIgZaycOKM5APiQxCYOHYcH1ddYFdaQRGLkLhYE3esuiRxsVNE_xM_Eq9aKg5InKzRPPM6yaQoHlbwqgJeve48ANcKAeStYlZJDqXQWt4uZgDQlFw3cLe4l9I6lwKUOClOGima7GbFr8sUepx8GBmOS5bo-5ZGS7nAfpd8YsGxaRWJmO3DSEtmz9-fJeZCZBG7zk-s9z8osk0ME_kxZYwTw0gsUs7NA1P4I-1uCnYVw0BsUQoJ7FmOGRh__jJPERtwnVM3KxpDhzEPYF_6cbm1vuvp5sbhfnHHYZ_oweE8LT6_fXM9vyivPry7nJ9dlVhzPZVLIIeuqrhS2vFW8bpVBKJV0PG2dtKBBE1WdZLLFivXZs8FCidq4KLr6tPiyT43v1X-Hmkyg0-W-h5HCttkWtBNLWvxX1jVSrdc6wxf7KGNIaVIzmyiHzDuTAXmZonmryVm_egQu-0GWh7tYWu5__jQx2SxdxFH69OR6aZRraozK_fMp4l-HtsYv5lG1Uqa68Uncz7_-PWCL8B8yf7p3qNNZh22Mf8D6Z8P-BvDC8AZ</recordid><startdate>1984</startdate><enddate>1984</enddate><creator>Leighton, John K</creator><creator>DeBrunner-Vossbrinck, Bettina A</creator><creator>Kemper, Byron</creator><general>American Chemical Society</general><scope>BSCLL</scope><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>7QL</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>1984</creationdate><title>Isolation and sequence analysis of three cloned cDNAs for rabbit liver proteins that are related to rabbit cytochrome P-450 (form 2), the major phenobarbital-inducible form</title><author>Leighton, John K ; DeBrunner-Vossbrinck, Bettina A ; Kemper, Byron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a329t-d0efaf112779f2872387e04870b283f5f0509ec7b5258a1f80ef24a4f43024bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cloning, Molecular</topic><topic>Codon - genetics</topic><topic>cytochrome P-450</topic><topic>Cytochrome P-450 Enzyme System - genetics</topic><topic>DNA - isolation & purification</topic><topic>Enzyme Induction</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>liver</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Methods. Procedures. Technologies</topic><topic>Microsomes, Liver - drug effects</topic><topic>Nucleic Acid Hybridization</topic><topic>nucleotide sequence</topic><topic>Phenobarbital - pharmacology</topic><topic>Plasmids</topic><topic>Rabbits</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leighton, John K</creatorcontrib><creatorcontrib>DeBrunner-Vossbrinck, Bettina A</creatorcontrib><creatorcontrib>Kemper, Byron</creatorcontrib><collection>Istex</collection><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemistry (Easton)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leighton, John K</au><au>DeBrunner-Vossbrinck, Bettina A</au><au>Kemper, Byron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation and sequence analysis of three cloned cDNAs for rabbit liver proteins that are related to rabbit cytochrome P-450 (form 2), the major phenobarbital-inducible form</atitle><jtitle>Biochemistry (Easton)</jtitle><addtitle>Biochemistry</addtitle><date>1984</date><risdate>1984</risdate><volume>23</volume><issue>2</issue><spage>204</spage><epage>210</epage><pages>204-210</pages><issn>0006-2960</issn><eissn>1520-4995</eissn><abstract>We have isolated from rabbit liver three cDNA clones of 1400-1800 base pairs that hybridize selectively to RNA from animals treated with phenobarbital. The nucleotide sequences of the cDNAs have been determined. In the protein coding region the nucleotide sequences of two of the cDNAs are 88% homologous, and the third cDNA is about 72-74% homologous to the other two. All three are 55-60% homologous to rat liver cytochrome P-450b cDNA. The amino acid sequences derived from the cDNA sequences are about 50% homologous to those of rat liver cytochrome P-450b and rabbit liver cytochrome P-450 (form 2). The degree of homology differs substantially in different regions of the protein. The hydrophobicity profiles of these five mammalian cytochromes P-450 are very similar and contain up to eight regions of hydrophobicity that are long enough to span a membrane. These results indicate that these three cDNAs code for rabbit liver cytochromes P-450 which are different from any rabbit liver cytochrome P-450 for which amino acid sequence information is published. These cDNAs are part of a family of genes that are related to rabbit liver cytochrome P-450 (form 2) and rat liver cytochrome P-450b which are the major phenobarbital-inducible forms. The divergence of amino acid sequence between the rat and rabbit forms and the divergence of nucleotide sequences of silent sites in the two most closely related rabbit forms suggest that cytochromes P-450 have a relatively high rate of amino acid divergence compared to many other vertebrate proteins.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>6546520</pmid><doi>10.1021/bi00297a005</doi><tpages>7</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Biological and medical sciences Biotechnology Cloning, Molecular Codon - genetics cytochrome P-450 Cytochrome P-450 Enzyme System - genetics DNA - isolation & purification Enzyme Induction Fundamental and applied biological sciences. Psychology Genes Genetic engineering Genetic technics liver Liver - metabolism Male Methods. Procedures. Technologies Microsomes, Liver - drug effects Nucleic Acid Hybridization nucleotide sequence Phenobarbital - pharmacology Plasmids Rabbits |
title | Isolation and sequence analysis of three cloned cDNAs for rabbit liver proteins that are related to rabbit cytochrome P-450 (form 2), the major phenobarbital-inducible form |
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