The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila
Polycomb group proteins are required for long-term repression of many genes in Drosophila and all metazoans. In Drosophila , DNA fragments called Polycomb-group response elements (PREs) have been identified that mediate the action of Polycomb-group proteins. Previous studies have shown that a 2 kb f...
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Veröffentlicht in: | Development (Cambridge) 2008-02, Vol.135 (4), p.669-676 |
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description | Polycomb group proteins are required for long-term repression of many genes in Drosophila and all metazoans. In Drosophila , DNA fragments called Polycomb-group response elements (PREs) have been identified that mediate the action of Polycomb-group proteins. Previous studies have shown that a 2 kb fragment located from -2.4 kb to -395 bp upstream of the Drosophila engrailed promoter contains a multipartite PRE that can mediate mini- white silencing and act as a PRE in an Ubx -reporter construct. Here, we study the role of this 2 kb fragment in the regulation of the engrailed gene itself. Our results show that within this 2 kb fragment, there are two subfragments that can act as PREs in embryos. In addition to their role in gene silencing, these two adjacent PRE fragments can facilitate the activation of the engrailed promoter by distant enhancers. The repressive action of the engrailed PRE can also act over a distance. A 181 bp subfragment can act as a PRE and also mediate positive effects in an enhancer-detector construct. Finally, a deletion of 530 bp of the 2 kb PRE fragment within the endogenous engrailed gene causes a loss-of-function phenotype, showing the importance of the positive regulatory effects of this PRE-containing fragment. Our data are consistent with the model that engrailed PREs bring chromatin together, allowing both positive and negative regulatory interactions between distantly located DNA fragments. |
doi_str_mv | 10.1242/dev.014779 |
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In Drosophila , DNA fragments called Polycomb-group response elements (PREs) have been identified that mediate the action of Polycomb-group proteins. Previous studies have shown that a 2 kb fragment located from -2.4 kb to -395 bp upstream of the Drosophila engrailed promoter contains a multipartite PRE that can mediate mini- white silencing and act as a PRE in an Ubx -reporter construct. Here, we study the role of this 2 kb fragment in the regulation of the engrailed gene itself. Our results show that within this 2 kb fragment, there are two subfragments that can act as PREs in embryos. In addition to their role in gene silencing, these two adjacent PRE fragments can facilitate the activation of the engrailed promoter by distant enhancers. The repressive action of the engrailed PRE can also act over a distance. A 181 bp subfragment can act as a PRE and also mediate positive effects in an enhancer-detector construct. Finally, a deletion of 530 bp of the 2 kb PRE fragment within the endogenous engrailed gene causes a loss-of-function phenotype, showing the importance of the positive regulatory effects of this PRE-containing fragment. Our data are consistent with the model that engrailed PREs bring chromatin together, allowing both positive and negative regulatory interactions between distantly located DNA fragments.</description><identifier>ISSN: 0950-1991</identifier><identifier>EISSN: 1477-9129</identifier><identifier>DOI: 10.1242/dev.014779</identifier><identifier>PMID: 18199580</identifier><language>eng</language><publisher>England: The Company of Biologists Limited</publisher><subject>Animals ; Base Pairing ; DNA - genetics ; Drosophila ; Drosophila melanogaster - embryology ; Drosophila melanogaster - genetics ; Embryo, Nonmammalian - metabolism ; Enhancer Elements, Genetic - genetics ; Gene Expression Regulation ; Genome ; Homeodomain Proteins - genetics ; Metazoa ; Phenotype ; Polycomb-Group Proteins ; Repressor Proteins - genetics ; Response Elements - genetics ; Sequence Deletion ; Silencer Elements, Transcriptional - genetics ; Transcription Factors - genetics ; Transcription, Genetic ; Wings, Animal - abnormalities</subject><ispartof>Development (Cambridge), 2008-02, Vol.135 (4), p.669-676</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-f9b6b0a795ae013155a544808ac7a67b8277ccb3e220c35cb36da1e2ef943ba73</citedby><cites>FETCH-LOGICAL-c353t-f9b6b0a795ae013155a544808ac7a67b8277ccb3e220c35cb36da1e2ef943ba73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3664,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18199580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DeVido, Sarah K</creatorcontrib><creatorcontrib>Kwon, Deborah</creatorcontrib><creatorcontrib>Brown, J Lesley</creatorcontrib><creatorcontrib>Kassis, Judith A</creatorcontrib><title>The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila</title><title>Development (Cambridge)</title><addtitle>Development</addtitle><description>Polycomb group proteins are required for long-term repression of many genes in Drosophila and all metazoans. In Drosophila , DNA fragments called Polycomb-group response elements (PREs) have been identified that mediate the action of Polycomb-group proteins. Previous studies have shown that a 2 kb fragment located from -2.4 kb to -395 bp upstream of the Drosophila engrailed promoter contains a multipartite PRE that can mediate mini- white silencing and act as a PRE in an Ubx -reporter construct. Here, we study the role of this 2 kb fragment in the regulation of the engrailed gene itself. Our results show that within this 2 kb fragment, there are two subfragments that can act as PREs in embryos. In addition to their role in gene silencing, these two adjacent PRE fragments can facilitate the activation of the engrailed promoter by distant enhancers. The repressive action of the engrailed PRE can also act over a distance. A 181 bp subfragment can act as a PRE and also mediate positive effects in an enhancer-detector construct. Finally, a deletion of 530 bp of the 2 kb PRE fragment within the endogenous engrailed gene causes a loss-of-function phenotype, showing the importance of the positive regulatory effects of this PRE-containing fragment. Our data are consistent with the model that engrailed PREs bring chromatin together, allowing both positive and negative regulatory interactions between distantly located DNA fragments.</description><subject>Animals</subject><subject>Base Pairing</subject><subject>DNA - genetics</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila melanogaster - genetics</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Enhancer Elements, Genetic - genetics</subject><subject>Gene Expression Regulation</subject><subject>Genome</subject><subject>Homeodomain Proteins - genetics</subject><subject>Metazoa</subject><subject>Phenotype</subject><subject>Polycomb-Group Proteins</subject><subject>Repressor Proteins - genetics</subject><subject>Response Elements - genetics</subject><subject>Sequence Deletion</subject><subject>Silencer Elements, Transcriptional - genetics</subject><subject>Transcription Factors - genetics</subject><subject>Transcription, Genetic</subject><subject>Wings, Animal - abnormalities</subject><issn>0950-1991</issn><issn>1477-9129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtPwzAQhC0EglK48ANQThwQKX4kcXxE5SlVgkM5W467SY2cONgJqP8el1biyGlWu9-MtIPQBcEzQjN6u4KvGSYZ5-IATbaaCkLFIZpgkeOUCEFO0GkIHxhjVnB-jE5IGbd5iSdIL9eQeGchcXXy5uxGu7ZKG-_GPvEQetcFSMBCC90QEtPFZTNaNRjXbR3QNV4ZC6tk8KoL2pv-9xTBe--C69fGqjN0VCsb4HyvU_T--LCcP6eL16eX-d0i1SxnQ1qLqqiw4iJXgAkjea7yLCtxqTRXBa9KyrnWFQNKcXTEqVgpAhRqkbFKcTZFV7vc3rvPEcIgWxM0WKs6cGOQHFMmqCj-BYkoS4aLMoLXO1DHZ4KHWvbetMpvJMFy272M3ctd9xG-3KeOVQurP3RfdgRudsDaNOtv40FWxlnXmDCEbRBY10vCcpnJohDsB200kKM</recordid><startdate>200802</startdate><enddate>200802</enddate><creator>DeVido, Sarah K</creator><creator>Kwon, Deborah</creator><creator>Brown, J Lesley</creator><creator>Kassis, Judith A</creator><general>The Company of Biologists Limited</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>7SS</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200802</creationdate><title>The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila</title><author>DeVido, Sarah K ; Kwon, Deborah ; Brown, J Lesley ; Kassis, Judith A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-f9b6b0a795ae013155a544808ac7a67b8277ccb3e220c35cb36da1e2ef943ba73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Base Pairing</topic><topic>DNA - genetics</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - embryology</topic><topic>Drosophila melanogaster - genetics</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Enhancer Elements, Genetic - genetics</topic><topic>Gene Expression Regulation</topic><topic>Genome</topic><topic>Homeodomain Proteins - genetics</topic><topic>Metazoa</topic><topic>Phenotype</topic><topic>Polycomb-Group Proteins</topic><topic>Repressor Proteins - genetics</topic><topic>Response Elements - genetics</topic><topic>Sequence Deletion</topic><topic>Silencer Elements, Transcriptional - genetics</topic><topic>Transcription Factors - genetics</topic><topic>Transcription, Genetic</topic><topic>Wings, Animal - abnormalities</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DeVido, Sarah K</creatorcontrib><creatorcontrib>Kwon, Deborah</creatorcontrib><creatorcontrib>Brown, J Lesley</creatorcontrib><creatorcontrib>Kassis, Judith A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Nucleic Acids Abstracts</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>Development (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DeVido, Sarah K</au><au>Kwon, Deborah</au><au>Brown, J Lesley</au><au>Kassis, Judith A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila</atitle><jtitle>Development (Cambridge)</jtitle><addtitle>Development</addtitle><date>2008-02</date><risdate>2008</risdate><volume>135</volume><issue>4</issue><spage>669</spage><epage>676</epage><pages>669-676</pages><issn>0950-1991</issn><eissn>1477-9129</eissn><abstract>Polycomb group proteins are required for long-term repression of many genes in Drosophila and all metazoans. In Drosophila , DNA fragments called Polycomb-group response elements (PREs) have been identified that mediate the action of Polycomb-group proteins. Previous studies have shown that a 2 kb fragment located from -2.4 kb to -395 bp upstream of the Drosophila engrailed promoter contains a multipartite PRE that can mediate mini- white silencing and act as a PRE in an Ubx -reporter construct. Here, we study the role of this 2 kb fragment in the regulation of the engrailed gene itself. Our results show that within this 2 kb fragment, there are two subfragments that can act as PREs in embryos. In addition to their role in gene silencing, these two adjacent PRE fragments can facilitate the activation of the engrailed promoter by distant enhancers. The repressive action of the engrailed PRE can also act over a distance. A 181 bp subfragment can act as a PRE and also mediate positive effects in an enhancer-detector construct. Finally, a deletion of 530 bp of the 2 kb PRE fragment within the endogenous engrailed gene causes a loss-of-function phenotype, showing the importance of the positive regulatory effects of this PRE-containing fragment. Our data are consistent with the model that engrailed PREs bring chromatin together, allowing both positive and negative regulatory interactions between distantly located DNA fragments.</abstract><cop>England</cop><pub>The Company of Biologists Limited</pub><pmid>18199580</pmid><doi>10.1242/dev.014779</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Base Pairing DNA - genetics Drosophila Drosophila melanogaster - embryology Drosophila melanogaster - genetics Embryo, Nonmammalian - metabolism Enhancer Elements, Genetic - genetics Gene Expression Regulation Genome Homeodomain Proteins - genetics Metazoa Phenotype Polycomb-Group Proteins Repressor Proteins - genetics Response Elements - genetics Sequence Deletion Silencer Elements, Transcriptional - genetics Transcription Factors - genetics Transcription, Genetic Wings, Animal - abnormalities |
title | The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila |
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