Rap1 and Canoe/afadin are essential for establishment of apical-basal polarity in the Drosophila embryo
The establishment and maintenance of apical-basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization....
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Veröffentlicht in: | Molecular biology of the cell 2013-04, Vol.24 (7), p.945-963 |
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description | The establishment and maintenance of apical-basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization. Bazooka then helps to position both adherens junctions and atypical protein kinase C (aPKC). Although a polarized cytoskeleton is critical for Bazooka positioning, proteins mediating this remained unknown. We found that the small GTPase Rap1 and the actin-junctional linker Canoe/afadin are essential for polarity establishment, as both adherens junctions and Bazooka are mispositioned in their absence. Rap1 and Canoe do not simply organize the cytoskeleton, as actin and microtubules become properly polarized in their absence. Canoe can recruit Bazooka when ectopically expressed, but they do not obligatorily colocalize. Rap1 and Canoe play continuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore apical Bazooka in the absence of Rap1 or Canoe. We next tested the current linear model for polarity establishment. Both Bazooka and aPKC regulate Canoe localization despite being "downstream" of Canoe. Further, Rap1, Bazooka, and aPKC, but not Canoe, regulate columnar cell shape. These data reshape our view, suggesting that polarity establishment is regulated by a protein network rather than a linear pathway. |
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Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization. Bazooka then helps to position both adherens junctions and atypical protein kinase C (aPKC). Although a polarized cytoskeleton is critical for Bazooka positioning, proteins mediating this remained unknown. We found that the small GTPase Rap1 and the actin-junctional linker Canoe/afadin are essential for polarity establishment, as both adherens junctions and Bazooka are mispositioned in their absence. Rap1 and Canoe do not simply organize the cytoskeleton, as actin and microtubules become properly polarized in their absence. Canoe can recruit Bazooka when ectopically expressed, but they do not obligatorily colocalize. Rap1 and Canoe play continuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore apical Bazooka in the absence of Rap1 or Canoe. We next tested the current linear model for polarity establishment. Both Bazooka and aPKC regulate Canoe localization despite being "downstream" of Canoe. Further, Rap1, Bazooka, and aPKC, but not Canoe, regulate columnar cell shape. These data reshape our view, suggesting that polarity establishment is regulated by a protein network rather than a linear pathway.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.E12-10-0736</identifier><identifier>PMID: 23363604</identifier><language>eng</language><publisher>United States: American Society for Cell Biology</publisher><subject>Adherens Junctions - metabolism ; Animals ; BASIC BIOLOGICAL SCIENCES ; Cell biology ; Cell Line ; Cell Polarity ; Cell Shape ; Cytoskeleton - metabolism ; Drosophila melanogaster - embryology ; Drosophila melanogaster - genetics ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Embryo, Nonmammalian - cytology ; Embryo, Nonmammalian - embryology ; Embryo, Nonmammalian - metabolism ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Microscopy, Confocal ; Models, Biological ; Mutation ; Protein Kinase C - genetics ; Protein Kinase C - metabolism ; rap1 GTP-Binding Proteins - genetics ; rap1 GTP-Binding Proteins - metabolism ; RNA Interference</subject><ispartof>Molecular biology of the cell, 2013-04, Vol.24 (7), p.945-963</ispartof><rights>2013 Choi This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License ( ). 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-f7e39e6771ad14d80288661bec6a9cff549912bb7b89225cccb0aff368f9c1b53</citedby><cites>FETCH-LOGICAL-c425t-f7e39e6771ad14d80288661bec6a9cff549912bb7b89225cccb0aff368f9c1b53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608504/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608504/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23363604$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1625230$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><contributor>Montell, Denise</contributor><creatorcontrib>Choi, Wangsun</creatorcontrib><creatorcontrib>Harris, Nathan J</creatorcontrib><creatorcontrib>Sumigray, Kaelyn D</creatorcontrib><creatorcontrib>Peifer, Mark</creatorcontrib><creatorcontrib>Univ. of North Carolina, Chapel Hill, NC (United States)</creatorcontrib><title>Rap1 and Canoe/afadin are essential for establishment of apical-basal polarity in the Drosophila embryo</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>The establishment and maintenance of apical-basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization. Bazooka then helps to position both adherens junctions and atypical protein kinase C (aPKC). Although a polarized cytoskeleton is critical for Bazooka positioning, proteins mediating this remained unknown. We found that the small GTPase Rap1 and the actin-junctional linker Canoe/afadin are essential for polarity establishment, as both adherens junctions and Bazooka are mispositioned in their absence. Rap1 and Canoe do not simply organize the cytoskeleton, as actin and microtubules become properly polarized in their absence. Canoe can recruit Bazooka when ectopically expressed, but they do not obligatorily colocalize. Rap1 and Canoe play continuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore apical Bazooka in the absence of Rap1 or Canoe. We next tested the current linear model for polarity establishment. Both Bazooka and aPKC regulate Canoe localization despite being "downstream" of Canoe. Further, Rap1, Bazooka, and aPKC, but not Canoe, regulate columnar cell shape. These data reshape our view, suggesting that polarity establishment is regulated by a protein network rather than a linear pathway.</description><subject>Adherens Junctions - metabolism</subject><subject>Animals</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Cell biology</subject><subject>Cell Line</subject><subject>Cell Polarity</subject><subject>Cell Shape</subject><subject>Cytoskeleton - metabolism</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Embryo, Nonmammalian - cytology</subject><subject>Embryo, Nonmammalian - embryology</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Microscopy, Confocal</subject><subject>Models, Biological</subject><subject>Mutation</subject><subject>Protein Kinase C - genetics</subject><subject>Protein Kinase C - metabolism</subject><subject>rap1 GTP-Binding Proteins - genetics</subject><subject>rap1 GTP-Binding Proteins - metabolism</subject><subject>RNA Interference</subject><issn>1059-1524</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1v1DAQxSMEoqVw5oYsTlzS9fgr8QUJLeVDqoSE4GyNHbsxSuJgZyvtf49XWyo42WP_5nn8XtO8BnoNVMNutu76BlgLtKUdV0-aS9Bct0L26mndU6lbkExcNC9K-UUpCKG6580F41xxRcVlc_cdVyC4DGSPS_I7DDjEhWD2xJfily3iRELKtdrQTrGMcz0kKRBco8OptVgqsaYJc9yOpPZuoycfcyppHeOExM82H9PL5lnAqfhXD-tV8_PTzY_9l_b22-ev-w-3rRNMbm3oPNdedR3gAGLoKet7pcB6p1C7EKTQGpi1ne01Y9I5ZymGwFUftAMr-VXz_qy7HuzsB1eHzTiZNccZ89EkjOb_myWO5i7dm2pHL6moAm_PAqls0RQXN-9Gl5bFu82AYpJxWqF3D6_k9PtQrTFzLM5PEy4-HYoBzoBzqTpe0d0ZddWSkn14nAWoOWVoaobGAzvVpwxrx5t_v_DI_w2N_wFO5pm-</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Choi, Wangsun</creator><creator>Harris, Nathan J</creator><creator>Sumigray, Kaelyn D</creator><creator>Peifer, Mark</creator><general>American Society for Cell Biology</general><general>The American Society for Cell Biology</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>7X8</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>20130401</creationdate><title>Rap1 and Canoe/afadin are essential for establishment of apical-basal polarity in the Drosophila embryo</title><author>Choi, Wangsun ; Harris, Nathan J ; Sumigray, Kaelyn D ; Peifer, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-f7e39e6771ad14d80288661bec6a9cff549912bb7b89225cccb0aff368f9c1b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adherens Junctions - metabolism</topic><topic>Animals</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Cell biology</topic><topic>Cell Line</topic><topic>Cell Polarity</topic><topic>Cell Shape</topic><topic>Cytoskeleton - metabolism</topic><topic>Drosophila melanogaster - embryology</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Embryo, Nonmammalian - cytology</topic><topic>Embryo, Nonmammalian - embryology</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Microscopy, Confocal</topic><topic>Models, Biological</topic><topic>Mutation</topic><topic>Protein Kinase C - genetics</topic><topic>Protein Kinase C - metabolism</topic><topic>rap1 GTP-Binding Proteins - genetics</topic><topic>rap1 GTP-Binding Proteins - metabolism</topic><topic>RNA Interference</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Wangsun</creatorcontrib><creatorcontrib>Harris, Nathan J</creatorcontrib><creatorcontrib>Sumigray, Kaelyn D</creatorcontrib><creatorcontrib>Peifer, Mark</creatorcontrib><creatorcontrib>Univ. of North Carolina, Chapel Hill, NC (United States)</creatorcontrib><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><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Wangsun</au><au>Harris, Nathan J</au><au>Sumigray, Kaelyn D</au><au>Peifer, Mark</au><au>Montell, Denise</au><aucorp>Univ. of North Carolina, Chapel Hill, NC (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rap1 and Canoe/afadin are essential for establishment of apical-basal polarity in the Drosophila embryo</atitle><jtitle>Molecular biology of the cell</jtitle><addtitle>Mol Biol Cell</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>24</volume><issue>7</issue><spage>945</spage><epage>963</epage><pages>945-963</pages><issn>1059-1524</issn><eissn>1939-4586</eissn><abstract>The establishment and maintenance of apical-basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization. Bazooka then helps to position both adherens junctions and atypical protein kinase C (aPKC). Although a polarized cytoskeleton is critical for Bazooka positioning, proteins mediating this remained unknown. We found that the small GTPase Rap1 and the actin-junctional linker Canoe/afadin are essential for polarity establishment, as both adherens junctions and Bazooka are mispositioned in their absence. Rap1 and Canoe do not simply organize the cytoskeleton, as actin and microtubules become properly polarized in their absence. Canoe can recruit Bazooka when ectopically expressed, but they do not obligatorily colocalize. Rap1 and Canoe play continuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore apical Bazooka in the absence of Rap1 or Canoe. We next tested the current linear model for polarity establishment. Both Bazooka and aPKC regulate Canoe localization despite being "downstream" of Canoe. Further, Rap1, Bazooka, and aPKC, but not Canoe, regulate columnar cell shape. These data reshape our view, suggesting that polarity establishment is regulated by a protein network rather than a linear pathway.</abstract><cop>United States</cop><pub>American Society for Cell Biology</pub><pmid>23363604</pmid><doi>10.1091/mbc.E12-10-0736</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adherens Junctions - metabolism Animals BASIC BIOLOGICAL SCIENCES Cell biology Cell Line Cell Polarity Cell Shape Cytoskeleton - metabolism Drosophila melanogaster - embryology Drosophila melanogaster - genetics Drosophila melanogaster - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism Embryo, Nonmammalian - cytology Embryo, Nonmammalian - embryology Embryo, Nonmammalian - metabolism Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism Microscopy, Confocal Models, Biological Mutation Protein Kinase C - genetics Protein Kinase C - metabolism rap1 GTP-Binding Proteins - genetics rap1 GTP-Binding Proteins - metabolism RNA Interference |
title | Rap1 and Canoe/afadin are essential for establishment of apical-basal polarity in the Drosophila embryo |
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