Conservation between animals and plants of the cis-acting element involved in the unfolded protein response
Using Arabidopsis thaliana, we identified the cis-element involved in the plant unfolded protein response (UPR). In transgenic plants, tunicamycin stimulated expression of a reporter gene under the control of the BiP promoter and promoter analysis identified a 24 bp sequence crucial to this inductio...
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| Veröffentlicht in: | Biochemical and biophysical research communications 2003-01, Vol.301 (1), p.225-230 |
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| container_title | Biochemical and biophysical research communications |
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| creator | Oh, Dong-Ha Kwon, Chang-Seob Sano, Hiroshi Chung, Won-Il Koizumi, Nozomu |
| description | Using
Arabidopsis thaliana, we identified the
cis-element involved in the plant unfolded protein response (UPR). In transgenic plants, tunicamycin stimulated expression of a reporter gene under the control of the BiP promoter and promoter analysis identified a 24
bp sequence crucial to this induction. When fused with a minimal promoter, a hexamer of this sequence was sufficient for induction of a reporter gene in protoplasts treated with tunicamycin or dithiothreitol. Induction rate equivalent to original promoter was observed when the assay was conducted in transgenic plants. This 24
bp sequence contained two elements also responsible for the UPR in animals. Either of these elements was sufficient for the plant UPR, indicating conservation between animals and plants of
cis-elements involved in the UPR. |
| doi_str_mv | 10.1016/S0006-291X(02)03019-X |
| format | Article |
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Arabidopsis thaliana, we identified the
cis-element involved in the plant unfolded protein response (UPR). In transgenic plants, tunicamycin stimulated expression of a reporter gene under the control of the BiP promoter and promoter analysis identified a 24
bp sequence crucial to this induction. When fused with a minimal promoter, a hexamer of this sequence was sufficient for induction of a reporter gene in protoplasts treated with tunicamycin or dithiothreitol. Induction rate equivalent to original promoter was observed when the assay was conducted in transgenic plants. This 24
bp sequence contained two elements also responsible for the UPR in animals. Either of these elements was sufficient for the plant UPR, indicating conservation between animals and plants of
cis-elements involved in the UPR.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/S0006-291X(02)03019-X</identifier><identifier>PMID: 12535667</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Bacterial Agents - pharmacology ; Arabidopsis - drug effects ; Arabidopsis - genetics ; Arabidopsis - physiology ; Arabidopsis thaliana ; Base Sequence ; BiP ; cis-Element ; Gene Expression Regulation ; Genes, Plant ; Genes, Reporter ; Molecular Sequence Data ; Mutation ; Plants, Genetically Modified ; Promoter ; Promoter Regions, Genetic ; Protein Folding ; Tunicamycin ; Tunicamycin - pharmacology ; UPR</subject><ispartof>Biochemical and biophysical research communications, 2003-01, Vol.301 (1), p.225-230</ispartof><rights>2002 Elsevier Science (USA)</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-819628a47a504159c9d8ddd724ee20fd5832e91cfcdb928fdcad193e55b5fb53</citedby><cites>FETCH-LOGICAL-c458t-819628a47a504159c9d8ddd724ee20fd5832e91cfcdb928fdcad193e55b5fb53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X0203019X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12535667$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oh, Dong-Ha</creatorcontrib><creatorcontrib>Kwon, Chang-Seob</creatorcontrib><creatorcontrib>Sano, Hiroshi</creatorcontrib><creatorcontrib>Chung, Won-Il</creatorcontrib><creatorcontrib>Koizumi, Nozomu</creatorcontrib><title>Conservation between animals and plants of the cis-acting element involved in the unfolded protein response</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Using
Arabidopsis thaliana, we identified the
cis-element involved in the plant unfolded protein response (UPR). In transgenic plants, tunicamycin stimulated expression of a reporter gene under the control of the BiP promoter and promoter analysis identified a 24
bp sequence crucial to this induction. When fused with a minimal promoter, a hexamer of this sequence was sufficient for induction of a reporter gene in protoplasts treated with tunicamycin or dithiothreitol. Induction rate equivalent to original promoter was observed when the assay was conducted in transgenic plants. This 24
bp sequence contained two elements also responsible for the UPR in animals. Either of these elements was sufficient for the plant UPR, indicating conservation between animals and plants of
cis-elements involved in the UPR.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Arabidopsis - drug effects</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - physiology</subject><subject>Arabidopsis thaliana</subject><subject>Base Sequence</subject><subject>BiP</subject><subject>cis-Element</subject><subject>Gene Expression Regulation</subject><subject>Genes, Plant</subject><subject>Genes, Reporter</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Plants, Genetically Modified</subject><subject>Promoter</subject><subject>Promoter Regions, Genetic</subject><subject>Protein Folding</subject><subject>Tunicamycin</subject><subject>Tunicamycin - pharmacology</subject><subject>UPR</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkbtOxDAQRS0EguXxCaBUCIrA2ImTuEJoxUtCooBiOyuxJ2DI2ovtXcTf430ISqqZsc7Mle8l5JjCBQVaXT4DQJUzQSdnwM6hACryyRYZURCQMwrlNhn9IntkP4R3AErLSuySPcp4wauqHpGPsbMB_aKNxtmsw_iFaLPWmmk7hFR1NhtaG0Pm-iy-YaZMyFsVjX3NcMAp2pgZu3DDAnVqVsjc9m7QaZ55FzE9egyzpcoh2enTVTza1APycnvzMr7PH5_uHsbXj7kqeRPzhoqKNW1ZtxxKyoUSutFa16xEZNBr3hQMBVW90p1gTa9Vq6kokPOO9x0vDsjp-mzS_5xjiHJqgsIh_QPdPMiaCS6YgH9B2lScN7VIIF-DyrsQPPZy5pNB_ltSkMs05CoNubRaApOrNOQk7Z1sBObdFPXf1sb-BFytAUx2LAx6GZRBq1AbjypK7cw_Ej9jBpxW</recordid><startdate>20030131</startdate><enddate>20030131</enddate><creator>Oh, Dong-Ha</creator><creator>Kwon, Chang-Seob</creator><creator>Sano, Hiroshi</creator><creator>Chung, Won-Il</creator><creator>Koizumi, Nozomu</creator><general>Elsevier Inc</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>7TM</scope><scope>7X8</scope></search><sort><creationdate>20030131</creationdate><title>Conservation between animals and plants of the cis-acting element involved in the unfolded protein response</title><author>Oh, Dong-Ha ; Kwon, Chang-Seob ; Sano, Hiroshi ; Chung, Won-Il ; Koizumi, Nozomu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-819628a47a504159c9d8ddd724ee20fd5832e91cfcdb928fdcad193e55b5fb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Arabidopsis - drug effects</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - physiology</topic><topic>Arabidopsis thaliana</topic><topic>Base Sequence</topic><topic>BiP</topic><topic>cis-Element</topic><topic>Gene Expression Regulation</topic><topic>Genes, Plant</topic><topic>Genes, Reporter</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Plants, Genetically Modified</topic><topic>Promoter</topic><topic>Promoter Regions, Genetic</topic><topic>Protein Folding</topic><topic>Tunicamycin</topic><topic>Tunicamycin - pharmacology</topic><topic>UPR</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oh, Dong-Ha</creatorcontrib><creatorcontrib>Kwon, Chang-Seob</creatorcontrib><creatorcontrib>Sano, Hiroshi</creatorcontrib><creatorcontrib>Chung, Won-Il</creatorcontrib><creatorcontrib>Koizumi, Nozomu</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oh, Dong-Ha</au><au>Kwon, Chang-Seob</au><au>Sano, Hiroshi</au><au>Chung, Won-Il</au><au>Koizumi, Nozomu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conservation between animals and plants of the cis-acting element involved in the unfolded protein response</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2003-01-31</date><risdate>2003</risdate><volume>301</volume><issue>1</issue><spage>225</spage><epage>230</epage><pages>225-230</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Using
Arabidopsis thaliana, we identified the
cis-element involved in the plant unfolded protein response (UPR). In transgenic plants, tunicamycin stimulated expression of a reporter gene under the control of the BiP promoter and promoter analysis identified a 24
bp sequence crucial to this induction. When fused with a minimal promoter, a hexamer of this sequence was sufficient for induction of a reporter gene in protoplasts treated with tunicamycin or dithiothreitol. Induction rate equivalent to original promoter was observed when the assay was conducted in transgenic plants. This 24
bp sequence contained two elements also responsible for the UPR in animals. Either of these elements was sufficient for the plant UPR, indicating conservation between animals and plants of
cis-elements involved in the UPR.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12535667</pmid><doi>10.1016/S0006-291X(02)03019-X</doi><tpages>6</tpages></addata></record> |
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| source | MEDLINE; ScienceDirect Freedom Collection (Elsevier) |
| subjects | Animals Anti-Bacterial Agents - pharmacology Arabidopsis - drug effects Arabidopsis - genetics Arabidopsis - physiology Arabidopsis thaliana Base Sequence BiP cis-Element Gene Expression Regulation Genes, Plant Genes, Reporter Molecular Sequence Data Mutation Plants, Genetically Modified Promoter Promoter Regions, Genetic Protein Folding Tunicamycin Tunicamycin - pharmacology UPR |
| title | Conservation between animals and plants of the cis-acting element involved in the unfolded protein response |
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