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Plastid promoter utilization in a rice embryogenic cell culture
Plastid promoter utilization was characterized in rice by mapping transcript 5'-ends in samples derived from leaves and cultured embryogenic cells. We have found that rbcL, atpB and the rRNA operon are transcribed by the plastid-encoded plastid RNA polymerase (PEP), while clpP is transcribed by...
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Published in: | Current genetics 1998-07, Vol.34 (1), p.67-70 |
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creator | Silhavy, D Maliga, P |
description | Plastid promoter utilization was characterized in rice by mapping transcript 5'-ends in samples derived from leaves and cultured embryogenic cells. We have found that rbcL, atpB and the rRNA operon are transcribed by the plastid-encoded plastid RNA polymerase (PEP), while clpP is transcribed by the nucleus-encoded plastid RNA polymerase (NEP) in both chloroplasts and the non-green plastids of embryogenic cultured cells. This finding is in contrast to reports on BY2 tobacco, in which NEP promoter activity in cultured cells was enhanced relative to leaves, facilitating identification of NEP promoters which are undetectable in chloroplasts. Therefore, it appears that activation of plastid NEP promoters in rice is not essential for adaptation to cell culture. |
doi_str_mv | 10.1007/s002940050367 |
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We have found that rbcL, atpB and the rRNA operon are transcribed by the plastid-encoded plastid RNA polymerase (PEP), while clpP is transcribed by the nucleus-encoded plastid RNA polymerase (NEP) in both chloroplasts and the non-green plastids of embryogenic cultured cells. This finding is in contrast to reports on BY2 tobacco, in which NEP promoter activity in cultured cells was enhanced relative to leaves, facilitating identification of NEP promoters which are undetectable in chloroplasts. Therefore, it appears that activation of plastid NEP promoters in rice is not essential for adaptation to cell culture.</description><identifier>ISSN: 0172-8083</identifier><identifier>EISSN: 1432-0983</identifier><identifier>DOI: 10.1007/s002940050367</identifier><identifier>PMID: 9683677</identifier><language>eng</language><publisher>United States</publisher><subject>Adenosine Triphosphatases - genetics ; Base Sequence ; Cells, Cultured ; chloroplast DNA ; chloroplasts ; Chloroplasts - metabolism ; chromosome mapping ; cultured cells ; DNA, Plant - chemistry ; DNA-directed RNA polymerase ; DNA-Directed RNA Polymerases - genetics ; DNA-Directed RNA Polymerases - metabolism ; Endopeptidase Clp ; enzyme activity ; gene expression ; Histone-Lysine N-Methyltransferase - genetics ; leaves ; messenger RNA ; Nicotiana tabacum ; nucleotide sequences ; operon ; Oryza - embryology ; Oryza - genetics ; Oryza sativa ; Plant Leaves - chemistry ; plastids ; Plastids - genetics ; promoter regions ; Promoter Regions, Genetic ; ribosomal RNA ; RNA, Ribosomal, 16S - genetics ; Sequence Alignment ; Serine Endopeptidases ; somatic embryogenesis ; transcription (genetics) ; Transcription, Genetic</subject><ispartof>Current genetics, 1998-07, Vol.34 (1), p.67-70</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-1d0585cd9e909164a90a9351d21fd4357ac6914875dc56a878e73e4c31f915773</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9683677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silhavy, D</creatorcontrib><creatorcontrib>Maliga, P</creatorcontrib><title>Plastid promoter utilization in a rice embryogenic cell culture</title><title>Current genetics</title><addtitle>Curr Genet</addtitle><description>Plastid promoter utilization was characterized in rice by mapping transcript 5'-ends in samples derived from leaves and cultured embryogenic cells. We have found that rbcL, atpB and the rRNA operon are transcribed by the plastid-encoded plastid RNA polymerase (PEP), while clpP is transcribed by the nucleus-encoded plastid RNA polymerase (NEP) in both chloroplasts and the non-green plastids of embryogenic cultured cells. This finding is in contrast to reports on BY2 tobacco, in which NEP promoter activity in cultured cells was enhanced relative to leaves, facilitating identification of NEP promoters which are undetectable in chloroplasts. Therefore, it appears that activation of plastid NEP promoters in rice is not essential for adaptation to cell culture.</description><subject>Adenosine Triphosphatases - genetics</subject><subject>Base Sequence</subject><subject>Cells, Cultured</subject><subject>chloroplast DNA</subject><subject>chloroplasts</subject><subject>Chloroplasts - metabolism</subject><subject>chromosome mapping</subject><subject>cultured cells</subject><subject>DNA, Plant - chemistry</subject><subject>DNA-directed RNA polymerase</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>Endopeptidase Clp</subject><subject>enzyme activity</subject><subject>gene expression</subject><subject>Histone-Lysine N-Methyltransferase - genetics</subject><subject>leaves</subject><subject>messenger RNA</subject><subject>Nicotiana tabacum</subject><subject>nucleotide sequences</subject><subject>operon</subject><subject>Oryza - embryology</subject><subject>Oryza - genetics</subject><subject>Oryza sativa</subject><subject>Plant Leaves - chemistry</subject><subject>plastids</subject><subject>Plastids - genetics</subject><subject>promoter regions</subject><subject>Promoter Regions, Genetic</subject><subject>ribosomal RNA</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Sequence Alignment</subject><subject>Serine Endopeptidases</subject><subject>somatic embryogenesis</subject><subject>transcription (genetics)</subject><subject>Transcription, Genetic</subject><issn>0172-8083</issn><issn>1432-0983</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLAzEUhYMotVaXLsWs3I3em8ckWYkUX1BQ0K6HNJMpkXloMrOov94pLYIrV2dxPg6Hj5BzhGsEUDcJgBkBIIHn6oBMUXCWgdH8kEwBFcs0aH5MTlL6AECmjZqQicn1SKspuX2tbepDST9j13S9j3ToQx2-bR-6loaWWhqD89Q3q7jp1r4Njjpf19QNdT9Ef0qOKlsnf7bPGVk-3L_Pn7LFy-Pz_G6ROS54n2EJUktXGm_AYC6sAWu4xJJhVQoulXW5QaGVLJ3MrVbaK-6F41gZlErxGbna7Y4_vwaf-qIJaXvEtr4bUqEBBCrD_gVRIeco5QhmO9DFLqXoq-IzhsbGTYFQbM0Wf8yO_MV-eFg1vvyl9yrH_nLXV7Yr7DqGVCzfGCAHprVS0vAfvdl6zw</recordid><startdate>19980701</startdate><enddate>19980701</enddate><creator>Silhavy, D</creator><creator>Maliga, P</creator><scope>FBQ</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19980701</creationdate><title>Plastid promoter utilization in a rice embryogenic cell culture</title><author>Silhavy, D ; Maliga, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-1d0585cd9e909164a90a9351d21fd4357ac6914875dc56a878e73e4c31f915773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenosine Triphosphatases - genetics</topic><topic>Base Sequence</topic><topic>Cells, Cultured</topic><topic>chloroplast DNA</topic><topic>chloroplasts</topic><topic>Chloroplasts - metabolism</topic><topic>chromosome mapping</topic><topic>cultured cells</topic><topic>DNA, Plant - chemistry</topic><topic>DNA-directed RNA polymerase</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>Endopeptidase Clp</topic><topic>enzyme activity</topic><topic>gene expression</topic><topic>Histone-Lysine N-Methyltransferase - genetics</topic><topic>leaves</topic><topic>messenger RNA</topic><topic>Nicotiana tabacum</topic><topic>nucleotide sequences</topic><topic>operon</topic><topic>Oryza - embryology</topic><topic>Oryza - genetics</topic><topic>Oryza sativa</topic><topic>Plant Leaves - chemistry</topic><topic>plastids</topic><topic>Plastids - genetics</topic><topic>promoter regions</topic><topic>Promoter Regions, Genetic</topic><topic>ribosomal RNA</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Sequence Alignment</topic><topic>Serine Endopeptidases</topic><topic>somatic embryogenesis</topic><topic>transcription (genetics)</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silhavy, D</creatorcontrib><creatorcontrib>Maliga, P</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Current genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silhavy, D</au><au>Maliga, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plastid promoter utilization in a rice embryogenic cell culture</atitle><jtitle>Current genetics</jtitle><addtitle>Curr Genet</addtitle><date>1998-07-01</date><risdate>1998</risdate><volume>34</volume><issue>1</issue><spage>67</spage><epage>70</epage><pages>67-70</pages><issn>0172-8083</issn><eissn>1432-0983</eissn><abstract>Plastid promoter utilization was characterized in rice by mapping transcript 5'-ends in samples derived from leaves and cultured embryogenic cells. We have found that rbcL, atpB and the rRNA operon are transcribed by the plastid-encoded plastid RNA polymerase (PEP), while clpP is transcribed by the nucleus-encoded plastid RNA polymerase (NEP) in both chloroplasts and the non-green plastids of embryogenic cultured cells. This finding is in contrast to reports on BY2 tobacco, in which NEP promoter activity in cultured cells was enhanced relative to leaves, facilitating identification of NEP promoters which are undetectable in chloroplasts. Therefore, it appears that activation of plastid NEP promoters in rice is not essential for adaptation to cell culture.</abstract><cop>United States</cop><pmid>9683677</pmid><doi>10.1007/s002940050367</doi><tpages>4</tpages></addata></record> |
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subjects | Adenosine Triphosphatases - genetics Base Sequence Cells, Cultured chloroplast DNA chloroplasts Chloroplasts - metabolism chromosome mapping cultured cells DNA, Plant - chemistry DNA-directed RNA polymerase DNA-Directed RNA Polymerases - genetics DNA-Directed RNA Polymerases - metabolism Endopeptidase Clp enzyme activity gene expression Histone-Lysine N-Methyltransferase - genetics leaves messenger RNA Nicotiana tabacum nucleotide sequences operon Oryza - embryology Oryza - genetics Oryza sativa Plant Leaves - chemistry plastids Plastids - genetics promoter regions Promoter Regions, Genetic ribosomal RNA RNA, Ribosomal, 16S - genetics Sequence Alignment Serine Endopeptidases somatic embryogenesis transcription (genetics) Transcription, Genetic |
title | Plastid promoter utilization in a rice embryogenic cell culture |
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