Aner Gurvitz , Leila Wabnegger , Hanspeter Rottensteiner , Ian W Dawes , Andreas Hartig , Helmut Ruis , Barbara Hamilton
{"title":"油酸诱导酵母基因SPS19编码过氧化物酶体β-氧化辅酶2,4-二烯酰辅酶a还原酶的adr1p依赖性调控","authors":"Aner Gurvitz , Leila Wabnegger , Hanspeter Rottensteiner , Ian W Dawes , Andreas Hartig , Helmut Ruis , Barbara Hamilton","doi":"10.1006/mcbr.2000.0261","DOIUrl":null,"url":null,"abstract":"<div><p>The role of <em>Saccharomyces cerevisiae</em> Adr1p was examined with respect to the transcriptional regulation of the <em>SPS19</em> gene encoding the peroxisomal β-oxidation auxiliary enzyme 2,4-dienoyl-CoA reductase. The <em>SPS19</em> promoter contains both an oleate response element that binds the Pip2p-Oaf1p transcription factor as well as a canonical Adr1p-binding element, termed UAS1<sub>SPS19</sub>. Northern analysis demonstrated that transcriptional up-regulation of <em>SPS19</em> was abolished in cells devoid of Adr1p. Expression of an <em>SPS19-lacZ</em> reporter gene was shown to be quiescent in the <em>adr1</em>Δ mutant and abnormally elevated in cells containing multiple <em>ADR1</em> copies. UAS1<sub>SPS19</sub> was able to compete for formation of a specific complex between recombinant Adr1p-LacZ and UAS1<sub>CTA1</sub> representing the corresponding Adr1p-binding element in the promoter of the catalase A gene, and to interact directly with this fusion protein. We conclude that in the presence of fatty acids in the medium transcription of <em>SPS19</em> is directly regulated by both Pip2p-Oaf1p and Adr1p.</p></div>","PeriodicalId":80086,"journal":{"name":"Molecular cell biology research communications : MCBRC","volume":"4 2","pages":"Pages 81-89"},"PeriodicalIF":0.0000,"publicationDate":"2000-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/mcbr.2000.0261","citationCount":"25","resultStr":"{\"title\":\"Adr1p-Dependent Regulation of the Oleic Acid-Inducible Yeast Gene SPS19 Encoding the Peroxisomal β-Oxidation Auxiliary Enzyme 2,4-Dienoyl-CoA Reductase\",\"authors\":\"Aner Gurvitz , Leila Wabnegger , Hanspeter Rottensteiner , Ian W Dawes , Andreas Hartig , Helmut Ruis , Barbara Hamilton\",\"doi\":\"10.1006/mcbr.2000.0261\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The role of <em>Saccharomyces cerevisiae</em> Adr1p was examined with respect to the transcriptional regulation of the <em>SPS19</em> gene encoding the peroxisomal β-oxidation auxiliary enzyme 2,4-dienoyl-CoA reductase. The <em>SPS19</em> promoter contains both an oleate response element that binds the Pip2p-Oaf1p transcription factor as well as a canonical Adr1p-binding element, termed UAS1<sub>SPS19</sub>. Northern analysis demonstrated that transcriptional up-regulation of <em>SPS19</em> was abolished in cells devoid of Adr1p. Expression of an <em>SPS19-lacZ</em> reporter gene was shown to be quiescent in the <em>adr1</em>Δ mutant and abnormally elevated in cells containing multiple <em>ADR1</em> copies. UAS1<sub>SPS19</sub> was able to compete for formation of a specific complex between recombinant Adr1p-LacZ and UAS1<sub>CTA1</sub> representing the corresponding Adr1p-binding element in the promoter of the catalase A gene, and to interact directly with this fusion protein. We conclude that in the presence of fatty acids in the medium transcription of <em>SPS19</em> is directly regulated by both Pip2p-Oaf1p and Adr1p.</p></div>\",\"PeriodicalId\":80086,\"journal\":{\"name\":\"Molecular cell biology research communications : MCBRC\",\"volume\":\"4 2\",\"pages\":\"Pages 81-89\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1006/mcbr.2000.0261\",\"citationCount\":\"25\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular cell biology research communications : MCBRC\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1522472400902617\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular cell biology research communications : MCBRC","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1522472400902617","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Adr1p-Dependent Regulation of the Oleic Acid-Inducible Yeast Gene SPS19 Encoding the Peroxisomal β-Oxidation Auxiliary Enzyme 2,4-Dienoyl-CoA Reductase
The role of Saccharomyces cerevisiae Adr1p was examined with respect to the transcriptional regulation of the SPS19 gene encoding the peroxisomal β-oxidation auxiliary enzyme 2,4-dienoyl-CoA reductase. The SPS19 promoter contains both an oleate response element that binds the Pip2p-Oaf1p transcription factor as well as a canonical Adr1p-binding element, termed UAS1SPS19. Northern analysis demonstrated that transcriptional up-regulation of SPS19 was abolished in cells devoid of Adr1p. Expression of an SPS19-lacZ reporter gene was shown to be quiescent in the adr1Δ mutant and abnormally elevated in cells containing multiple ADR1 copies. UAS1SPS19 was able to compete for formation of a specific complex between recombinant Adr1p-LacZ and UAS1CTA1 representing the corresponding Adr1p-binding element in the promoter of the catalase A gene, and to interact directly with this fusion protein. We conclude that in the presence of fatty acids in the medium transcription of SPS19 is directly regulated by both Pip2p-Oaf1p and Adr1p.