Identification of short promoter regions involved in the transcriptional expression of the nitrate reductase gene in Chlamydomonas reinhardtii
In Chlamydomonas reinhardtii, the expression of the Nia1 gene encoding NAD(P)H nitrate reductase is controlled at the transcriptional level, positively by light and negatively by ammonium. Previous work has shown that the region -279 to +269 with respect to the start site of transcription was suffic...
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Veröffentlicht in: | Plant molecular biology 2001-01, Vol.45 (2), p.215-227 |
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description | In Chlamydomonas reinhardtii, the expression of the Nia1 gene encoding NAD(P)H nitrate reductase is controlled at the transcriptional level, positively by light and negatively by ammonium. Previous work has shown that the region -279 to +269 with respect to the start site of transcription was sufficient to confer regulated expression of a promoterless arylsulfatase (Ars) reporter gene. To understand the mechanisms underlying this regulation, the -279 to +2 sequence was analysed for the presence of ammonium-responsive elements using either pJD54 (promoterless Ars gene) or pJD100 (minimal beta-tubulin promoter-driven Ars gene). The region lying between -195 and -120 was shown to be dispensable. Essential responsive elements were found in four distinct regions between -231 and -219, -120 and -100, -76 and -65 and -33 and -8. Each of these sequences is required for maximal expression in the absence of ammonium and a conserved GGA/TAGGGT motif is present in two of these regions. Several deletions within the region -33 to -77 were shown to partially relieve the transformants from the negative effect of ammonium. These experiments demonstrate that Nia1 expression is promoted by at least four elements between -231 and -8 and suggest that part of the repression by ammonium takes place through a proximal element located in the -51 to -33 sequence. |
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Previous work has shown that the region -279 to +269 with respect to the start site of transcription was sufficient to confer regulated expression of a promoterless arylsulfatase (Ars) reporter gene. To understand the mechanisms underlying this regulation, the -279 to +2 sequence was analysed for the presence of ammonium-responsive elements using either pJD54 (promoterless Ars gene) or pJD100 (minimal beta-tubulin promoter-driven Ars gene). The region lying between -195 and -120 was shown to be dispensable. Essential responsive elements were found in four distinct regions between -231 and -219, -120 and -100, -76 and -65 and -33 and -8. Each of these sequences is required for maximal expression in the absence of ammonium and a conserved GGA/TAGGGT motif is present in two of these regions. Several deletions within the region -33 to -77 were shown to partially relieve the transformants from the negative effect of ammonium. These experiments demonstrate that Nia1 expression is promoted by at least four elements between -231 and -8 and suggest that part of the repression by ammonium takes place through a proximal element located in the -51 to -33 sequence.</description><identifier>ISSN: 0167-4412</identifier><identifier>EISSN: 1573-5028</identifier><identifier>DOI: 10.1023/A:1006401312916</identifier><identifier>PMID: 11289512</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Ammonium ; Animals ; aryl sulfatase ; Arylsulfatases - genetics ; Arylsulfatases - metabolism ; Bacteria ; Base Sequence ; Chlamydomonas reinhardtii ; Chlamydomonas reinhardtii - enzymology ; Chlamydomonas reinhardtii - genetics ; DNA - genetics ; DNA, Recombinant ; Enzymes ; Gene Expression Regulation, Enzymologic ; Molecular Sequence Data ; NAD(P)H nitrate reductase ; nia1 gene ; Nitrate Reductase ; Nitrate Reductases - genetics ; Plasmids - genetics ; Promoter Regions, Genetic - genetics ; Sequence Deletion ; Transcription, Genetic ; Transformation, Genetic</subject><ispartof>Plant molecular biology, 2001-01, Vol.45 (2), p.215-227</ispartof><rights>Kluwer Academic Publishers 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-12af06a51681b9547966d78cd14badd916c75820acddd68209cffa1eaa47de113</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11289512$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Loppes, R</creatorcontrib><creatorcontrib>Radoux, M</creatorcontrib><title>Identification of short promoter regions involved in the transcriptional expression of the nitrate reductase gene in Chlamydomonas reinhardtii</title><title>Plant molecular biology</title><addtitle>Plant Mol Biol</addtitle><description>In Chlamydomonas reinhardtii, the expression of the Nia1 gene encoding NAD(P)H nitrate reductase is controlled at the transcriptional level, positively by light and negatively by ammonium. Previous work has shown that the region -279 to +269 with respect to the start site of transcription was sufficient to confer regulated expression of a promoterless arylsulfatase (Ars) reporter gene. To understand the mechanisms underlying this regulation, the -279 to +2 sequence was analysed for the presence of ammonium-responsive elements using either pJD54 (promoterless Ars gene) or pJD100 (minimal beta-tubulin promoter-driven Ars gene). The region lying between -195 and -120 was shown to be dispensable. Essential responsive elements were found in four distinct regions between -231 and -219, -120 and -100, -76 and -65 and -33 and -8. Each of these sequences is required for maximal expression in the absence of ammonium and a conserved GGA/TAGGGT motif is present in two of these regions. Several deletions within the region -33 to -77 were shown to partially relieve the transformants from the negative effect of ammonium. These experiments demonstrate that Nia1 expression is promoted by at least four elements between -231 and -8 and suggest that part of the repression by ammonium takes place through a proximal element located in the -51 to -33 sequence.</description><subject>Ammonium</subject><subject>Animals</subject><subject>aryl sulfatase</subject><subject>Arylsulfatases - genetics</subject><subject>Arylsulfatases - metabolism</subject><subject>Bacteria</subject><subject>Base Sequence</subject><subject>Chlamydomonas reinhardtii</subject><subject>Chlamydomonas reinhardtii - enzymology</subject><subject>Chlamydomonas reinhardtii - genetics</subject><subject>DNA - genetics</subject><subject>DNA, Recombinant</subject><subject>Enzymes</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Molecular Sequence Data</subject><subject>NAD(P)H nitrate reductase</subject><subject>nia1 gene</subject><subject>Nitrate Reductase</subject><subject>Nitrate Reductases - genetics</subject><subject>Plasmids - genetics</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Sequence Deletion</subject><subject>Transcription, Genetic</subject><subject>Transformation, Genetic</subject><issn>0167-4412</issn><issn>1573-5028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkT9v2zAQxYkiQe2mnbMFRIZuSniURErZDKN_DATIks7GmTzFDCTKJSmj_hL5zKFbd8mS6R5wv3uHe8fYJYgbELK8XdyBEKoSUIJsQX1gc6h1WdRCNmdsLkDpoqpAztinGJ-FyHCpPrIZgGzaGuScvaws-eQ6ZzC50fOx43E7hsR3YRzGRIEHesqNyJ3fj_2ebBY8bYmngD6a4HbHOew5_dkFivFkciS8y0yi7GAnkzASfyJPx_nltsfhYPMGjzH3nd9isMm5z-y8wz7Sl1O9YL--f3tc_izuH36slov7wpQAqQCJnVBYg2pg09aVbpWyujEWqg1am5Mwum6kQGOtVVm0pusQCLHSlgDKC_b1n28-8_dEMa0HFw31PXoap7jWOqfbyuZdEHQjdSt0Bq_fgM_jFHIwf820Bqlkhq5O0LQZyK53wQ0YDuv__yhfAUKvj-A</recordid><startdate>200101</startdate><enddate>200101</enddate><creator>Loppes, R</creator><creator>Radoux, M</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>3V.</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>F1W</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>200101</creationdate><title>Identification of short promoter regions involved in the transcriptional expression of the nitrate reductase gene in Chlamydomonas reinhardtii</title><author>Loppes, R ; Radoux, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-12af06a51681b9547966d78cd14badd916c75820acddd68209cffa1eaa47de113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Ammonium</topic><topic>Animals</topic><topic>aryl sulfatase</topic><topic>Arylsulfatases - genetics</topic><topic>Arylsulfatases - metabolism</topic><topic>Bacteria</topic><topic>Base Sequence</topic><topic>Chlamydomonas reinhardtii</topic><topic>Chlamydomonas reinhardtii - enzymology</topic><topic>Chlamydomonas reinhardtii - genetics</topic><topic>DNA - genetics</topic><topic>DNA, Recombinant</topic><topic>Enzymes</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Molecular Sequence Data</topic><topic>NAD(P)H nitrate reductase</topic><topic>nia1 gene</topic><topic>Nitrate Reductase</topic><topic>Nitrate Reductases - genetics</topic><topic>Plasmids - genetics</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Sequence Deletion</topic><topic>Transcription, Genetic</topic><topic>Transformation, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Loppes, R</creatorcontrib><creatorcontrib>Radoux, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids 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>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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Research Library Prep</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>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Plant molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Loppes, R</au><au>Radoux, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of short promoter regions involved in the transcriptional expression of the nitrate reductase gene in Chlamydomonas reinhardtii</atitle><jtitle>Plant molecular biology</jtitle><addtitle>Plant Mol Biol</addtitle><date>2001-01</date><risdate>2001</risdate><volume>45</volume><issue>2</issue><spage>215</spage><epage>227</epage><pages>215-227</pages><issn>0167-4412</issn><eissn>1573-5028</eissn><abstract>In Chlamydomonas reinhardtii, the expression of the Nia1 gene encoding NAD(P)H nitrate reductase is controlled at the transcriptional level, positively by light and negatively by ammonium. Previous work has shown that the region -279 to +269 with respect to the start site of transcription was sufficient to confer regulated expression of a promoterless arylsulfatase (Ars) reporter gene. To understand the mechanisms underlying this regulation, the -279 to +2 sequence was analysed for the presence of ammonium-responsive elements using either pJD54 (promoterless Ars gene) or pJD100 (minimal beta-tubulin promoter-driven Ars gene). The region lying between -195 and -120 was shown to be dispensable. Essential responsive elements were found in four distinct regions between -231 and -219, -120 and -100, -76 and -65 and -33 and -8. Each of these sequences is required for maximal expression in the absence of ammonium and a conserved GGA/TAGGGT motif is present in two of these regions. Several deletions within the region -33 to -77 were shown to partially relieve the transformants from the negative effect of ammonium. These experiments demonstrate that Nia1 expression is promoted by at least four elements between -231 and -8 and suggest that part of the repression by ammonium takes place through a proximal element located in the -51 to -33 sequence.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>11289512</pmid><doi>10.1023/A:1006401312916</doi><tpages>13</tpages></addata></record> |
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subjects | Ammonium Animals aryl sulfatase Arylsulfatases - genetics Arylsulfatases - metabolism Bacteria Base Sequence Chlamydomonas reinhardtii Chlamydomonas reinhardtii - enzymology Chlamydomonas reinhardtii - genetics DNA - genetics DNA, Recombinant Enzymes Gene Expression Regulation, Enzymologic Molecular Sequence Data NAD(P)H nitrate reductase nia1 gene Nitrate Reductase Nitrate Reductases - genetics Plasmids - genetics Promoter Regions, Genetic - genetics Sequence Deletion Transcription, Genetic Transformation, Genetic |
title | Identification of short promoter regions involved in the transcriptional expression of the nitrate reductase gene in Chlamydomonas reinhardtii |
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