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The gang of four gene regulates growth and patterning of the developing Drosophila eye
We report here the identification of a novel complementation group in the fruit fly Drosophila melanogaster named gang of four (gfr). Mutations in gfr disrupt patterns of cell differentiation in the eye and increase eye size through a proliferative mechanism that can be enhanced by a block in apopto...
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Published in: | Fly (Austin, Tex.) Tex.), 2010-04, Vol.4 (2), p.104-116 |
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description | We report here the identification of a novel complementation group in the fruit fly Drosophila melanogaster named gang of four (gfr). Mutations in gfr disrupt patterns of cell differentiation in the eye and increase eye size through a proliferative mechanism that can be enhanced by a block in apoptosis. gfr mutant cells show several features of deregulated Ras/MAP kinase activity, including reduced expression of the Capicua growth suppressing transcription factor and synthetically lethality with alleles of the Jun N-terminal kinase phosphatase puckered. gfr alleles also upreguate Notch activity in the eye. Thus, gfr alleles appear to elicit growth and patterning phenotypes via effects on multiple signaling pathways. Moreover, the gfr alleles behave as gain-of-function lesions and overexpress the gene bruno-3 (bru-3), which is located at the genomic region to which gfr lesions map. Genetic reduction of bru-3 suppresses phenotypes caused by gfr alleles, and like gfr alleles, overexpression of bru-3 depresses levels of Cic protein, indicating that overexpression of bru-3 is central to gfr mutant phenotypes. |
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Mutations in gfr disrupt patterns of cell differentiation in the eye and increase eye size through a proliferative mechanism that can be enhanced by a block in apoptosis. gfr mutant cells show several features of deregulated Ras/MAP kinase activity, including reduced expression of the Capicua growth suppressing transcription factor and synthetically lethality with alleles of the Jun N-terminal kinase phosphatase puckered. gfr alleles also upreguate Notch activity in the eye. Thus, gfr alleles appear to elicit growth and patterning phenotypes via effects on multiple signaling pathways. Moreover, the gfr alleles behave as gain-of-function lesions and overexpress the gene bruno-3 (bru-3), which is located at the genomic region to which gfr lesions map. Genetic reduction of bru-3 suppresses phenotypes caused by gfr alleles, and like gfr alleles, overexpression of bru-3 depresses levels of Cic protein, indicating that overexpression of bru-3 is central to gfr mutant phenotypes.</description><identifier>ISSN: 1933-6934</identifier><identifier>ISSN: 1933-6942</identifier><identifier>EISSN: 1933-6942</identifier><identifier>DOI: 10.4161/fly.4.2.11890</identifier><identifier>PMID: 20473027</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Alleles ; Animals ; Animals, Genetically Modified ; apoptosis ; Base Sequence ; Binding ; Biology ; Bioscience ; Body Patterning - genetics ; Calcium ; Cancer ; Cell ; Cell Death - genetics ; cell differentiation ; cells ; Chromosome Mapping ; Cycle ; death ; DNA Primers - genetics ; Drosophila melanogaster ; Drosophila melanogaster - genetics ; Drosophila melanogaster - growth & development ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Eye - growth & development ; Eye - metabolism ; eyes ; Female ; fruit flies ; gain-of-function mutation ; Gene Expression Regulation, Developmental ; Genes, Insect ; Genetic Complementation Test ; genomics ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Landes ; Male ; MAP Kinase Signaling System - genetics ; mitogen-activated protein kinase ; Models, Biological ; mutants ; Mutation ; Organogenesis ; Phenotype ; Phosphoprotein Phosphatases - genetics ; Phosphoprotein Phosphatases - metabolism ; Proteins ; Receptors, Notch - genetics ; Receptors, Notch - metabolism ; signal transduction ; transcription factors ; Wings, Animal - growth & development ; Wings, Animal - metabolism</subject><ispartof>Fly (Austin, Tex.), 2010-04, Vol.4 (2), p.104-116</ispartof><rights>Copyright © 2010 Landes Bioscience 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-7ff4c6d6306e4e8c4b750357270e9825cb701b2700034bd93a75bd41b8a756593</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908041/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908041/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20473027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beam, Carolyn K.</creatorcontrib><creatorcontrib>Moberg, Kenneth H.</creatorcontrib><title>The gang of four gene regulates growth and patterning of the developing Drosophila eye</title><title>Fly (Austin, Tex.)</title><addtitle>Fly (Austin)</addtitle><description>We report here the identification of a novel complementation group in the fruit fly Drosophila melanogaster named gang of four (gfr). Mutations in gfr disrupt patterns of cell differentiation in the eye and increase eye size through a proliferative mechanism that can be enhanced by a block in apoptosis. gfr mutant cells show several features of deregulated Ras/MAP kinase activity, including reduced expression of the Capicua growth suppressing transcription factor and synthetically lethality with alleles of the Jun N-terminal kinase phosphatase puckered. gfr alleles also upreguate Notch activity in the eye. Thus, gfr alleles appear to elicit growth and patterning phenotypes via effects on multiple signaling pathways. Moreover, the gfr alleles behave as gain-of-function lesions and overexpress the gene bruno-3 (bru-3), which is located at the genomic region to which gfr lesions map. Genetic reduction of bru-3 suppresses phenotypes caused by gfr alleles, and like gfr alleles, overexpression of bru-3 depresses levels of Cic protein, indicating that overexpression of bru-3 is central to gfr mutant phenotypes.</description><subject>Alleles</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>apoptosis</subject><subject>Base Sequence</subject><subject>Binding</subject><subject>Biology</subject><subject>Bioscience</subject><subject>Body Patterning - genetics</subject><subject>Calcium</subject><subject>Cancer</subject><subject>Cell</subject><subject>Cell Death - genetics</subject><subject>cell differentiation</subject><subject>cells</subject><subject>Chromosome Mapping</subject><subject>Cycle</subject><subject>death</subject><subject>DNA Primers - genetics</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Eye - growth & development</subject><subject>Eye - metabolism</subject><subject>eyes</subject><subject>Female</subject><subject>fruit flies</subject><subject>gain-of-function mutation</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genes, Insect</subject><subject>Genetic Complementation Test</subject><subject>genomics</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Landes</subject><subject>Male</subject><subject>MAP Kinase Signaling System - genetics</subject><subject>mitogen-activated protein kinase</subject><subject>Models, Biological</subject><subject>mutants</subject><subject>Mutation</subject><subject>Organogenesis</subject><subject>Phenotype</subject><subject>Phosphoprotein Phosphatases - genetics</subject><subject>Phosphoprotein Phosphatases - metabolism</subject><subject>Proteins</subject><subject>Receptors, Notch - genetics</subject><subject>Receptors, Notch - metabolism</subject><subject>signal transduction</subject><subject>transcription factors</subject><subject>Wings, Animal - growth & development</subject><subject>Wings, Animal - metabolism</subject><issn>1933-6934</issn><issn>1933-6942</issn><issn>1933-6942</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkc2P1SAUxRujccbRpVvTnW765Kul3Zjo6KjJS9yMJq4IpZc-DIUKdCbvv5dnx0YToysu8LuHczlF8RSjHcMNfqntccd2ZIdx26F7xTnuKK2ajpH7W03ZWfEoxm8I1bxG9cPijCDGKSL8vPhyfYBylG4svS61X0I5goMywLhYmSCWY_C36VBKN5SzTAmCMyuccuMAN2D9fDp5G3z088FYWcIRHhcPtLQRntytF8Xnq3fXlx-q_af3Hy9f7ytVY5oqrjVTzdBQ1ACDVrE-G6Q1JxxB15Ja9RzhPu8QoqwfOip53Q8M920umrqjF8WrVXde-gkGBS4FacUczCTDUXhpxJ83zhzE6G8E6VCLGM4Cz-8Egv--QExiMlGBtdKBX6LglFLEEGeZfPFPkrDsuGlxQzJarajKnxID6M0QRuKUmsipCSaI-Jla5p_9PsVG_4opA3gF8mMDxN74qAw4BRt6EpQhGWVhE_1fD6LiDcjpav_1ZGUedO5p1x7jtA-TvPXBDiLJo_VBB-mUiYL-fYYfHxnKyg</recordid><startdate>20100401</startdate><enddate>20100401</enddate><creator>Beam, Carolyn K.</creator><creator>Moberg, Kenneth H.</creator><general>Taylor & Francis</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>7S9</scope><scope>L.6</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20100401</creationdate><title>The gang of four gene regulates growth and patterning of the developing Drosophila eye</title><author>Beam, Carolyn K. ; Moberg, Kenneth H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-7ff4c6d6306e4e8c4b750357270e9825cb701b2700034bd93a75bd41b8a756593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Alleles</topic><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>apoptosis</topic><topic>Base Sequence</topic><topic>Binding</topic><topic>Biology</topic><topic>Bioscience</topic><topic>Body Patterning - genetics</topic><topic>Calcium</topic><topic>Cancer</topic><topic>Cell</topic><topic>Cell Death - genetics</topic><topic>cell differentiation</topic><topic>cells</topic><topic>Chromosome Mapping</topic><topic>Cycle</topic><topic>death</topic><topic>DNA Primers - genetics</topic><topic>Drosophila melanogaster</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Eye - growth & development</topic><topic>Eye - metabolism</topic><topic>eyes</topic><topic>Female</topic><topic>fruit flies</topic><topic>gain-of-function mutation</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genes, Insect</topic><topic>Genetic Complementation Test</topic><topic>genomics</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Landes</topic><topic>Male</topic><topic>MAP Kinase Signaling System - genetics</topic><topic>mitogen-activated protein kinase</topic><topic>Models, Biological</topic><topic>mutants</topic><topic>Mutation</topic><topic>Organogenesis</topic><topic>Phenotype</topic><topic>Phosphoprotein Phosphatases - genetics</topic><topic>Phosphoprotein Phosphatases - metabolism</topic><topic>Proteins</topic><topic>Receptors, Notch - genetics</topic><topic>Receptors, Notch - metabolism</topic><topic>signal transduction</topic><topic>transcription factors</topic><topic>Wings, Animal - growth & development</topic><topic>Wings, Animal - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beam, Carolyn K.</creatorcontrib><creatorcontrib>Moberg, Kenneth H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Fly (Austin, Tex.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beam, Carolyn K.</au><au>Moberg, Kenneth H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The gang of four gene regulates growth and patterning of the developing Drosophila eye</atitle><jtitle>Fly (Austin, Tex.)</jtitle><addtitle>Fly (Austin)</addtitle><date>2010-04-01</date><risdate>2010</risdate><volume>4</volume><issue>2</issue><spage>104</spage><epage>116</epage><pages>104-116</pages><issn>1933-6934</issn><issn>1933-6942</issn><eissn>1933-6942</eissn><abstract>We report here the identification of a novel complementation group in the fruit fly Drosophila melanogaster named gang of four (gfr). Mutations in gfr disrupt patterns of cell differentiation in the eye and increase eye size through a proliferative mechanism that can be enhanced by a block in apoptosis. gfr mutant cells show several features of deregulated Ras/MAP kinase activity, including reduced expression of the Capicua growth suppressing transcription factor and synthetically lethality with alleles of the Jun N-terminal kinase phosphatase puckered. gfr alleles also upreguate Notch activity in the eye. Thus, gfr alleles appear to elicit growth and patterning phenotypes via effects on multiple signaling pathways. Moreover, the gfr alleles behave as gain-of-function lesions and overexpress the gene bruno-3 (bru-3), which is located at the genomic region to which gfr lesions map. Genetic reduction of bru-3 suppresses phenotypes caused by gfr alleles, and like gfr alleles, overexpression of bru-3 depresses levels of Cic protein, indicating that overexpression of bru-3 is central to gfr mutant phenotypes.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>20473027</pmid><doi>10.4161/fly.4.2.11890</doi><tpages>13</tpages></addata></record> |
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subjects | Alleles Animals Animals, Genetically Modified apoptosis Base Sequence Binding Biology Bioscience Body Patterning - genetics Calcium Cancer Cell Cell Death - genetics cell differentiation cells Chromosome Mapping Cycle death DNA Primers - genetics Drosophila melanogaster Drosophila melanogaster - genetics Drosophila melanogaster - growth & development Drosophila melanogaster - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism Eye - growth & development Eye - metabolism eyes Female fruit flies gain-of-function mutation Gene Expression Regulation, Developmental Genes, Insect Genetic Complementation Test genomics Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Landes Male MAP Kinase Signaling System - genetics mitogen-activated protein kinase Models, Biological mutants Mutation Organogenesis Phenotype Phosphoprotein Phosphatases - genetics Phosphoprotein Phosphatases - metabolism Proteins Receptors, Notch - genetics Receptors, Notch - metabolism signal transduction transcription factors Wings, Animal - growth & development Wings, Animal - metabolism |
title | The gang of four gene regulates growth and patterning of the developing Drosophila eye |
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