Cloning and sequencing hybrid striped bass (Morone saxatilis x M. chrysops) transforming growth factor-β (TGF-β), and development of a reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay to measure TGF-β mRNA of teleost fish
A transforming growth factor (TGF)-β was isolated and cloned from hybrid striped bass (Morone saxatilis x M. chrysops) anterior kidney mononuclear cells. This isolate (Genbank accession number AF140363) contains an open reading frame of 1146 bases coding for a 382 amino acid protein most similar to...
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Veröffentlicht in: | Fish & shellfish immunology 2000-01, Vol.10 (1), p.61-85 |
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creator | Harms, C.A Kennedy-Stoskopf, S Horne, W.A Fuller, F.J Tompkins, W.A.F |
description | A transforming growth factor (TGF)-β was isolated and cloned from hybrid striped bass (Morone saxatilis x M. chrysops) anterior kidney mononuclear cells. This isolate (Genbank accession number AF140363) contains an open reading frame of 1146 bases coding for a 382 amino acid protein most similar to rainbow trout TGF-β (57·3 and 78·6% identity with precursor and active protein, respectively) and rat TGF-β1(41·1 and 68·8% identity with precursor and active protein, respectively). Consensus primers were demonstrated to amplify specifically by polymerase chain reaction (PCR), a TGF-β segment from 14 species of teleost fish comprising 10 taxonomic families in 7 orders. A reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay was devised to measure TGF-β mRNA expression in teleost fish. Higher levels of TGF-β mRNA expression were detected in mononuclear cells of peripheral blood than from spleen or anterior kidney. |
doi_str_mv | 10.1006/fsim.1999.0230 |
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This isolate (Genbank accession number AF140363) contains an open reading frame of 1146 bases coding for a 382 amino acid protein most similar to rainbow trout TGF-β (57·3 and 78·6% identity with precursor and active protein, respectively) and rat TGF-β1(41·1 and 68·8% identity with precursor and active protein, respectively). Consensus primers were demonstrated to amplify specifically by polymerase chain reaction (PCR), a TGF-β segment from 14 species of teleost fish comprising 10 taxonomic families in 7 orders. A reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay was devised to measure TGF-β mRNA expression in teleost fish. Higher levels of TGF-β mRNA expression were detected in mononuclear cells of peripheral blood than from spleen or anterior kidney.</description><identifier>ISSN: 1050-4648</identifier><identifier>EISSN: 1095-9947</identifier><identifier>DOI: 10.1006/fsim.1999.0230</identifier><identifier>PMID: 10938723</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Bass - metabolism ; Blotting, Northern - veterinary ; Blotting, Southern - veterinary ; Chimera - genetics ; Cloning, Molecular ; Consensus Sequence ; Humans ; Kidney - chemistry ; Molecular Sequence Data ; Morone chrysops ; Morone saxatilis ; Oncorhynchus mykiss ; Rats ; Reverse Transcriptase Polymerase Chain Reaction - methods ; RNA, Messenger - analysis ; Teleostei ; Transforming Growth Factor beta - genetics ; transforming growth factor- beta ; transforming growth factor-β, TGF-β, sequence, hybrid striped bass, Morone saxatilis X M. chrysops, quantitative PCR ; Xenopus</subject><ispartof>Fish & shellfish immunology, 2000-01, Vol.10 (1), p.61-85</ispartof><rights>2000 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-86e37b2ea63967c032284249ba22c6fcb6af8b8eba1863c11770cbd6826682143</citedby><cites>FETCH-LOGICAL-c371t-86e37b2ea63967c032284249ba22c6fcb6af8b8eba1863c11770cbd6826682143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/fsim.1999.0230$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10938723$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harms, C.A</creatorcontrib><creatorcontrib>Kennedy-Stoskopf, S</creatorcontrib><creatorcontrib>Horne, W.A</creatorcontrib><creatorcontrib>Fuller, F.J</creatorcontrib><creatorcontrib>Tompkins, W.A.F</creatorcontrib><title>Cloning and sequencing hybrid striped bass (Morone saxatilis x M. chrysops) transforming growth factor-β (TGF-β), and development of a reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay to measure TGF-β mRNA of teleost fish</title><title>Fish & shellfish immunology</title><addtitle>Fish Shellfish Immunol</addtitle><description>A transforming growth factor (TGF)-β was isolated and cloned from hybrid striped bass (Morone saxatilis x M. chrysops) anterior kidney mononuclear cells. This isolate (Genbank accession number AF140363) contains an open reading frame of 1146 bases coding for a 382 amino acid protein most similar to rainbow trout TGF-β (57·3 and 78·6% identity with precursor and active protein, respectively) and rat TGF-β1(41·1 and 68·8% identity with precursor and active protein, respectively). Consensus primers were demonstrated to amplify specifically by polymerase chain reaction (PCR), a TGF-β segment from 14 species of teleost fish comprising 10 taxonomic families in 7 orders. A reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay was devised to measure TGF-β mRNA expression in teleost fish. Higher levels of TGF-β mRNA expression were detected in mononuclear cells of peripheral blood than from spleen or anterior kidney.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Bass - metabolism</subject><subject>Blotting, Northern - veterinary</subject><subject>Blotting, Southern - veterinary</subject><subject>Chimera - genetics</subject><subject>Cloning, Molecular</subject><subject>Consensus Sequence</subject><subject>Humans</subject><subject>Kidney - chemistry</subject><subject>Molecular Sequence Data</subject><subject>Morone chrysops</subject><subject>Morone saxatilis</subject><subject>Oncorhynchus mykiss</subject><subject>Rats</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>RNA, Messenger - analysis</subject><subject>Teleostei</subject><subject>Transforming Growth Factor beta - genetics</subject><subject>transforming growth factor- beta</subject><subject>transforming growth factor-β, TGF-β, sequence, hybrid striped bass, Morone saxatilis X M. chrysops, quantitative PCR</subject><subject>Xenopus</subject><issn>1050-4648</issn><issn>1095-9947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUs2O0zAQDgjEloUrRzSnVSuRYsepnRxXFbuLtAuoKufIcSZbo8RObbdsX4sH4ZnWIXvggjhY4xl9P6PRlyTvKFlSQvjH1ut-ScuyXJKMkefJjJJylZZlLl6M_xVJc54XZ8lr73-QSGCcvErOIogVImOzZ7N1Z4029yBNAx73BzRqbHen2uk4CU4P2EAtvYf5nXXWIHj5IIPutIcHuFuC2rmTt4NfQHDS-Na6flS4d_Zn2EErVbAu_f0L5tvrq1gXH_54NXjEzg49mgC2BQkuDpzHSURF26Ctgf1BmqBD9DsiKNsPGLvxP9ju1KOTkaF2UpvIj04jZb7Zpnv1bb1ZQNxaniBY6FH6g0OYVoB-8-VydA3YofUBWu13b5KXrew8vn2q58n3q0_b9U16-_X68_ryNlVM0JAWHJmoM5SclVwowrKsyLO8rGWWKd6qmsu2qAusJS04U5QKQVTd8CLj8dGcnScXk-7gbDy3D1WvvcKukwbtwVeCipwJTv4LpAURqxUTEbicgMpZ7x221eB0L92poqQaU1KNKanGlFRjSiLh_ZPyoe6x-Qs-xSICigmA8RBHja7ySsdkYKMdqlA1Vv9L-xFKI9H3</recordid><startdate>200001</startdate><enddate>200001</enddate><creator>Harms, C.A</creator><creator>Kennedy-Stoskopf, S</creator><creator>Horne, W.A</creator><creator>Fuller, F.J</creator><creator>Tompkins, W.A.F</creator><general>Elsevier 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>7T5</scope><scope>7TN</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200001</creationdate><title>Cloning and sequencing hybrid striped bass (Morone saxatilis x M. chrysops) transforming growth factor-β (TGF-β), and development of a reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay to measure TGF-β mRNA of teleost fish</title><author>Harms, C.A ; Kennedy-Stoskopf, S ; Horne, W.A ; Fuller, F.J ; Tompkins, W.A.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-86e37b2ea63967c032284249ba22c6fcb6af8b8eba1863c11770cbd6826682143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Bass - metabolism</topic><topic>Blotting, Northern - veterinary</topic><topic>Blotting, Southern - veterinary</topic><topic>Chimera - genetics</topic><topic>Cloning, Molecular</topic><topic>Consensus Sequence</topic><topic>Humans</topic><topic>Kidney - chemistry</topic><topic>Molecular Sequence Data</topic><topic>Morone chrysops</topic><topic>Morone saxatilis</topic><topic>Oncorhynchus mykiss</topic><topic>Rats</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - methods</topic><topic>RNA, Messenger - analysis</topic><topic>Teleostei</topic><topic>Transforming Growth Factor beta - genetics</topic><topic>transforming growth factor- beta</topic><topic>transforming growth factor-β, TGF-β, sequence, hybrid striped bass, Morone saxatilis X M. chrysops, quantitative PCR</topic><topic>Xenopus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harms, C.A</creatorcontrib><creatorcontrib>Kennedy-Stoskopf, S</creatorcontrib><creatorcontrib>Horne, W.A</creatorcontrib><creatorcontrib>Fuller, F.J</creatorcontrib><creatorcontrib>Tompkins, W.A.F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Fish & shellfish immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harms, C.A</au><au>Kennedy-Stoskopf, S</au><au>Horne, W.A</au><au>Fuller, F.J</au><au>Tompkins, W.A.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning and sequencing hybrid striped bass (Morone saxatilis x M. chrysops) transforming growth factor-β (TGF-β), and development of a reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay to measure TGF-β mRNA of teleost fish</atitle><jtitle>Fish & shellfish immunology</jtitle><addtitle>Fish Shellfish Immunol</addtitle><date>2000-01</date><risdate>2000</risdate><volume>10</volume><issue>1</issue><spage>61</spage><epage>85</epage><pages>61-85</pages><issn>1050-4648</issn><eissn>1095-9947</eissn><abstract>A transforming growth factor (TGF)-β was isolated and cloned from hybrid striped bass (Morone saxatilis x M. chrysops) anterior kidney mononuclear cells. This isolate (Genbank accession number AF140363) contains an open reading frame of 1146 bases coding for a 382 amino acid protein most similar to rainbow trout TGF-β (57·3 and 78·6% identity with precursor and active protein, respectively) and rat TGF-β1(41·1 and 68·8% identity with precursor and active protein, respectively). Consensus primers were demonstrated to amplify specifically by polymerase chain reaction (PCR), a TGF-β segment from 14 species of teleost fish comprising 10 taxonomic families in 7 orders. A reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay was devised to measure TGF-β mRNA expression in teleost fish. Higher levels of TGF-β mRNA expression were detected in mononuclear cells of peripheral blood than from spleen or anterior kidney.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>10938723</pmid><doi>10.1006/fsim.1999.0230</doi><tpages>25</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Bass - metabolism Blotting, Northern - veterinary Blotting, Southern - veterinary Chimera - genetics Cloning, Molecular Consensus Sequence Humans Kidney - chemistry Molecular Sequence Data Morone chrysops Morone saxatilis Oncorhynchus mykiss Rats Reverse Transcriptase Polymerase Chain Reaction - methods RNA, Messenger - analysis Teleostei Transforming Growth Factor beta - genetics transforming growth factor- beta transforming growth factor-β, TGF-β, sequence, hybrid striped bass, Morone saxatilis X M. chrysops, quantitative PCR Xenopus |
title | Cloning and sequencing hybrid striped bass (Morone saxatilis x M. chrysops) transforming growth factor-β (TGF-β), and development of a reverse transcription quantitative competitive polymerase chain reaction (RT-qcPCR) assay to measure TGF-β mRNA of teleost fish |
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