A dominant negative allele of the Drosophila leucine zipper protein Bunched blocks bunched function during tissue patterning
The bunched ( bun) gene encodes the Drosophila member of the TSC-22/GILZ family of leucine zipper transcriptional regulators. The bun locus encodes multiple BUN protein isoforms and has diverse roles during patterning of the eye, wing margin, dorsal notum and eggshell. Here we report the constructio...
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creator | Ash, David M. Hackney, Jennifer F. Jean-Francois, Michele Burton, Neal C. Dobens, Leonard L. |
description | The
bunched (
bun) gene encodes the Drosophila member of the TSC-22/GILZ family of leucine zipper transcriptional regulators. The
bun locus encodes multiple BUN protein isoforms and has diverse roles during patterning of the eye, wing margin, dorsal notum and eggshell. Here we report the construction and activity of a dominant negative allele (BunDN) of the BUN-B isoform. In the ovary, BunDN expression in the follicle cells (FC) resulted in epithelial defects including aberrant accumulation of DE-cadherin and failure to rearrange into columnar FC cell shapes. BunDN expression in the posterior FC led to loss of epithelial integrity associated with extensive apoptosis. BunDN FC phenotypes collectively resemble loss-of-function
bun mutant phenotypes. BunDN expression using tissue-specific imaginal disk drivers resulted in characteristic cuticular patterning defects that were enhanced by
bun mutations and suppressed by co-expression of the BUN-B protein isoform. These data indicate that BunDN has dominant negative activity useful to identify
bun functions and genetic interactions that occur during tissue patterning. |
doi_str_mv | 10.1016/j.mod.2007.05.003 |
format | Article |
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bunched (
bun) gene encodes the Drosophila member of the TSC-22/GILZ family of leucine zipper transcriptional regulators. The
bun locus encodes multiple BUN protein isoforms and has diverse roles during patterning of the eye, wing margin, dorsal notum and eggshell. Here we report the construction and activity of a dominant negative allele (BunDN) of the BUN-B isoform. In the ovary, BunDN expression in the follicle cells (FC) resulted in epithelial defects including aberrant accumulation of DE-cadherin and failure to rearrange into columnar FC cell shapes. BunDN expression in the posterior FC led to loss of epithelial integrity associated with extensive apoptosis. BunDN FC phenotypes collectively resemble loss-of-function
bun mutant phenotypes. BunDN expression using tissue-specific imaginal disk drivers resulted in characteristic cuticular patterning defects that were enhanced by
bun mutations and suppressed by co-expression of the BUN-B protein isoform. These data indicate that BunDN has dominant negative activity useful to identify
bun functions and genetic interactions that occur during tissue patterning.</description><identifier>ISSN: 0925-4773</identifier><identifier>EISSN: 1872-6356</identifier><identifier>DOI: 10.1016/j.mod.2007.05.003</identifier><identifier>PMID: 17600691</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Body Patterning ; Bunched ; Cadherins - metabolism ; Cell Shape ; Dominant negative ; Drosophila ; Drosophila - embryology ; Drosophila - metabolism ; Drosophila - physiology ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Epithelium - abnormalities ; Epithelium - embryology ; Epithelium - physiology ; Female ; GILZ ; Mutation ; Oogenesis ; Ovarian Follicle - cytology ; Ovarian Follicle - metabolism ; Tissue patterning ; TSC-22 ; TSC-22/GILZ family</subject><ispartof>Mechanisms of development, 2007-08, Vol.124 (7), p.559-569</ispartof><rights>2007</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-ee3dd3de0f334183975b82d24b7f57fad46b1172aeac3eb3ee3490c302daddae3</citedby><cites>FETCH-LOGICAL-c394t-ee3dd3de0f334183975b82d24b7f57fad46b1172aeac3eb3ee3490c302daddae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0925477307000986$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17600691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ash, David M.</creatorcontrib><creatorcontrib>Hackney, Jennifer F.</creatorcontrib><creatorcontrib>Jean-Francois, Michele</creatorcontrib><creatorcontrib>Burton, Neal C.</creatorcontrib><creatorcontrib>Dobens, Leonard L.</creatorcontrib><title>A dominant negative allele of the Drosophila leucine zipper protein Bunched blocks bunched function during tissue patterning</title><title>Mechanisms of development</title><addtitle>Mech Dev</addtitle><description>The
bunched (
bun) gene encodes the Drosophila member of the TSC-22/GILZ family of leucine zipper transcriptional regulators. The
bun locus encodes multiple BUN protein isoforms and has diverse roles during patterning of the eye, wing margin, dorsal notum and eggshell. Here we report the construction and activity of a dominant negative allele (BunDN) of the BUN-B isoform. In the ovary, BunDN expression in the follicle cells (FC) resulted in epithelial defects including aberrant accumulation of DE-cadherin and failure to rearrange into columnar FC cell shapes. BunDN expression in the posterior FC led to loss of epithelial integrity associated with extensive apoptosis. BunDN FC phenotypes collectively resemble loss-of-function
bun mutant phenotypes. BunDN expression using tissue-specific imaginal disk drivers resulted in characteristic cuticular patterning defects that were enhanced by
bun mutations and suppressed by co-expression of the BUN-B protein isoform. These data indicate that BunDN has dominant negative activity useful to identify
bun functions and genetic interactions that occur during tissue patterning.</description><subject>Animals</subject><subject>Body Patterning</subject><subject>Bunched</subject><subject>Cadherins - metabolism</subject><subject>Cell Shape</subject><subject>Dominant negative</subject><subject>Drosophila</subject><subject>Drosophila - embryology</subject><subject>Drosophila - metabolism</subject><subject>Drosophila - physiology</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Epithelium - abnormalities</subject><subject>Epithelium - embryology</subject><subject>Epithelium - physiology</subject><subject>Female</subject><subject>GILZ</subject><subject>Mutation</subject><subject>Oogenesis</subject><subject>Ovarian Follicle - cytology</subject><subject>Ovarian Follicle - metabolism</subject><subject>Tissue patterning</subject><subject>TSC-22</subject><subject>TSC-22/GILZ family</subject><issn>0925-4773</issn><issn>1872-6356</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFu1DAQhi0EotvCA3BBPnFLGMeJvRGnUqAgVeICZ8uxJ10vjh1spxKIh8fVrsSN02hG3_ya-Qh5xaBlwMTbY7tE23YAsoWhBeBPyI7tZdcIPoinZAdjNzS9lPyCXOZ8BADGBHtOLpgUAGJkO_Lnmtq4uKBDoQHvdXEPSLX36JHGmZYD0g8p5rgenNfU42ZcQPrbrSsmuqZY0AX6fgvmgJZOPpofmU7ndq61uBio3ZIL97S4nDekqy4FU6iTF-TZrH3Gl-d6Rb5_-vjt5nNz9_X2y831XWP42JcGkVvLLcLMec_2fJTDtO9s109yHuSsbS8mxmSnURuOE698P4Lh0FltrUZ-Rd6ccuvBPzfMRS0uG_ReB4xbVmLPukEIUUF2Ak39OSec1ZrcotMvxUA9KldHVZWrR-UKBlWV153X5_BtWtD-2zg7rsC7E4D1xQeHSWXjMBi0LqEpykb3n_i_MMyVHQ</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>Ash, David M.</creator><creator>Hackney, Jennifer F.</creator><creator>Jean-Francois, Michele</creator><creator>Burton, Neal C.</creator><creator>Dobens, Leonard L.</creator><general>Elsevier Ireland Ltd</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>20070801</creationdate><title>A dominant negative allele of the Drosophila leucine zipper protein Bunched blocks bunched function during tissue patterning</title><author>Ash, David M. ; Hackney, Jennifer F. ; Jean-Francois, Michele ; Burton, Neal C. ; Dobens, Leonard L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-ee3dd3de0f334183975b82d24b7f57fad46b1172aeac3eb3ee3490c302daddae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Body Patterning</topic><topic>Bunched</topic><topic>Cadherins - metabolism</topic><topic>Cell Shape</topic><topic>Dominant negative</topic><topic>Drosophila</topic><topic>Drosophila - embryology</topic><topic>Drosophila - metabolism</topic><topic>Drosophila - physiology</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Epithelium - abnormalities</topic><topic>Epithelium - embryology</topic><topic>Epithelium - physiology</topic><topic>Female</topic><topic>GILZ</topic><topic>Mutation</topic><topic>Oogenesis</topic><topic>Ovarian Follicle - cytology</topic><topic>Ovarian Follicle - metabolism</topic><topic>Tissue patterning</topic><topic>TSC-22</topic><topic>TSC-22/GILZ family</topic><toplevel>online_resources</toplevel><creatorcontrib>Ash, David M.</creatorcontrib><creatorcontrib>Hackney, Jennifer F.</creatorcontrib><creatorcontrib>Jean-Francois, Michele</creatorcontrib><creatorcontrib>Burton, Neal C.</creatorcontrib><creatorcontrib>Dobens, Leonard L.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Mechanisms of development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ash, David M.</au><au>Hackney, Jennifer F.</au><au>Jean-Francois, Michele</au><au>Burton, Neal C.</au><au>Dobens, Leonard L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A dominant negative allele of the Drosophila leucine zipper protein Bunched blocks bunched function during tissue patterning</atitle><jtitle>Mechanisms of development</jtitle><addtitle>Mech Dev</addtitle><date>2007-08-01</date><risdate>2007</risdate><volume>124</volume><issue>7</issue><spage>559</spage><epage>569</epage><pages>559-569</pages><issn>0925-4773</issn><eissn>1872-6356</eissn><abstract>The
bunched (
bun) gene encodes the Drosophila member of the TSC-22/GILZ family of leucine zipper transcriptional regulators. The
bun locus encodes multiple BUN protein isoforms and has diverse roles during patterning of the eye, wing margin, dorsal notum and eggshell. Here we report the construction and activity of a dominant negative allele (BunDN) of the BUN-B isoform. In the ovary, BunDN expression in the follicle cells (FC) resulted in epithelial defects including aberrant accumulation of DE-cadherin and failure to rearrange into columnar FC cell shapes. BunDN expression in the posterior FC led to loss of epithelial integrity associated with extensive apoptosis. BunDN FC phenotypes collectively resemble loss-of-function
bun mutant phenotypes. BunDN expression using tissue-specific imaginal disk drivers resulted in characteristic cuticular patterning defects that were enhanced by
bun mutations and suppressed by co-expression of the BUN-B protein isoform. These data indicate that BunDN has dominant negative activity useful to identify
bun functions and genetic interactions that occur during tissue patterning.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>17600691</pmid><doi>10.1016/j.mod.2007.05.003</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Animals Body Patterning Bunched Cadherins - metabolism Cell Shape Dominant negative Drosophila Drosophila - embryology Drosophila - metabolism Drosophila - physiology Drosophila Proteins - genetics Drosophila Proteins - metabolism Epithelium - abnormalities Epithelium - embryology Epithelium - physiology Female GILZ Mutation Oogenesis Ovarian Follicle - cytology Ovarian Follicle - metabolism Tissue patterning TSC-22 TSC-22/GILZ family |
title | A dominant negative allele of the Drosophila leucine zipper protein Bunched blocks bunched function during tissue patterning |
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