EndoGI modulates Notch signaling and axon guidance in Drosophila

Signaling through the Notch receptor has dramatically different effects depending on cell type and developmental timing. While a myriad of biological systems affected by Notch have been described, the molecular mechanisms by which a generic Notch signal is translated into a cell-type-specific output...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Mechanisms of development 2011-01, Vol.128 (1), p.59-70
Hauptverfasser: O’Keefe, David D., Edgar, Bruce A., Saucedo, Leslie J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 70
container_issue 1
container_start_page 59
container_title Mechanisms of development
container_volume 128
creator O’Keefe, David D.
Edgar, Bruce A.
Saucedo, Leslie J.
description Signaling through the Notch receptor has dramatically different effects depending on cell type and developmental timing. While a myriad of biological systems affected by Notch have been described, the molecular mechanisms by which a generic Notch signal is translated into a cell-type-specific output are less clear. Canonically, the Notch intracellular domain (NICD) translocates into the nucleus upon ligand binding to transcriptionally regulate target genes. In order to generate specificity, therefore, additional factors must exist that modulate NICD activity. Here we describe a novel regulator of the Notch pathway, Endonuclease GI (EndoGI). EndoGI localizes to the nucleus of most cells and activates Notch signaling when overexpressed. In the absence of endoGI, mutant animals are viable, but uncoordinated as motor neurons fail to innervate their appropriate muscle targets. Our data is therefore consistent with EndoGI functioning as a positive regulator of the Notch signaling pathway, playing a critical role during axon guidance of motor neurons.
doi_str_mv 10.1016/j.mod.2010.10.001
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3039039</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0925477310000808</els_id><sourcerecordid>1008827906</sourcerecordid><originalsourceid>FETCH-LOGICAL-c483t-6ddd5096eaf2dda12631b94937b289da8e734223f68275f91b649c8a809431c3</originalsourceid><addsrcrecordid>eNp9kUtLAzEUhYMoWh8_wI3MTjdT854EQRSfhaIb9yFNMm3KNKmTmaL_3tSq6EYIXJL73cPNOQAcIzhEEPHz-XAR7RDDz_sQQrQFBkhUuOSE8W0wgBKzklYV2QP7Kc1hJhBHu2API8gY5XQAru6CjQ-jIgv1je5cKp5iZ2ZF8tOgGx-mhQ620G8xFNPeWx2MK3wobtuY4nLmG30IdmrdJHf0VQ_Ay_3dy81jOX5-GN1cj0tDBelKbq1lUHKna2ytRpgTNJFUkmqChbRauIpQjEnNBa5YLdGEU2mEFlBSggw5AJcb2WU_WThrXOha3ahl6xe6fVdRe_W3E_xMTeNKEUhkPlng9Eugja-9S51a-GRc0-jgYp-UYKiiFWM8k2f_kghCkZeUcI2iDWqyH6l19c9CCKp1RGqusrNqHdH6KQeQZ05-_-Rn4juTDFxsAJftXHnXqmS8y8Zb3zrTKRv9P_IfDLeg3A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1008827906</pqid></control><display><type>article</type><title>EndoGI modulates Notch signaling and axon guidance in Drosophila</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>O’Keefe, David D. ; Edgar, Bruce A. ; Saucedo, Leslie J.</creator><creatorcontrib>O’Keefe, David D. ; Edgar, Bruce A. ; Saucedo, Leslie J.</creatorcontrib><description>Signaling through the Notch receptor has dramatically different effects depending on cell type and developmental timing. While a myriad of biological systems affected by Notch have been described, the molecular mechanisms by which a generic Notch signal is translated into a cell-type-specific output are less clear. Canonically, the Notch intracellular domain (NICD) translocates into the nucleus upon ligand binding to transcriptionally regulate target genes. In order to generate specificity, therefore, additional factors must exist that modulate NICD activity. Here we describe a novel regulator of the Notch pathway, Endonuclease GI (EndoGI). EndoGI localizes to the nucleus of most cells and activates Notch signaling when overexpressed. In the absence of endoGI, mutant animals are viable, but uncoordinated as motor neurons fail to innervate their appropriate muscle targets. Our data is therefore consistent with EndoGI functioning as a positive regulator of the Notch signaling pathway, playing a critical role during axon guidance of motor neurons.</description><identifier>ISSN: 0925-4773</identifier><identifier>EISSN: 1872-6356</identifier><identifier>DOI: 10.1016/j.mod.2010.10.001</identifier><identifier>PMID: 21055464</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Animals, Genetically Modified ; Axon guidance ; Axons - metabolism ; Axons - pathology ; Delta ; Drosophila ; Drosophila melanogaster - embryology ; Drosophila melanogaster - genetics ; Drosophila melanogaster - metabolism ; Drosophila melanogaster - ultrastructure ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Embryo, Nonmammalian - metabolism ; Embryo, Nonmammalian - pathology ; EndoGI ; Eye - growth &amp; development ; Eye - ultrastructure ; Female ; Genes, Insect - genetics ; Motor neuron ; Motor Neurons - metabolism ; Motor Neurons - pathology ; Notch ; Phenotype ; Protein Transport ; Receptors, Notch - metabolism ; Signal Transduction ; Tissue growth</subject><ispartof>Mechanisms of development, 2011-01, Vol.128 (1), p.59-70</ispartof><rights>2010 Elsevier Ireland Ltd</rights><rights>Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-6ddd5096eaf2dda12631b94937b289da8e734223f68275f91b649c8a809431c3</citedby><cites>FETCH-LOGICAL-c483t-6ddd5096eaf2dda12631b94937b289da8e734223f68275f91b649c8a809431c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mod.2010.10.001$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21055464$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O’Keefe, David D.</creatorcontrib><creatorcontrib>Edgar, Bruce A.</creatorcontrib><creatorcontrib>Saucedo, Leslie J.</creatorcontrib><title>EndoGI modulates Notch signaling and axon guidance in Drosophila</title><title>Mechanisms of development</title><addtitle>Mech Dev</addtitle><description>Signaling through the Notch receptor has dramatically different effects depending on cell type and developmental timing. While a myriad of biological systems affected by Notch have been described, the molecular mechanisms by which a generic Notch signal is translated into a cell-type-specific output are less clear. Canonically, the Notch intracellular domain (NICD) translocates into the nucleus upon ligand binding to transcriptionally regulate target genes. In order to generate specificity, therefore, additional factors must exist that modulate NICD activity. Here we describe a novel regulator of the Notch pathway, Endonuclease GI (EndoGI). EndoGI localizes to the nucleus of most cells and activates Notch signaling when overexpressed. In the absence of endoGI, mutant animals are viable, but uncoordinated as motor neurons fail to innervate their appropriate muscle targets. Our data is therefore consistent with EndoGI functioning as a positive regulator of the Notch signaling pathway, playing a critical role during axon guidance of motor neurons.</description><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Axon guidance</subject><subject>Axons - metabolism</subject><subject>Axons - pathology</subject><subject>Delta</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila melanogaster - ultrastructure</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Embryo, Nonmammalian - pathology</subject><subject>EndoGI</subject><subject>Eye - growth &amp; development</subject><subject>Eye - ultrastructure</subject><subject>Female</subject><subject>Genes, Insect - genetics</subject><subject>Motor neuron</subject><subject>Motor Neurons - metabolism</subject><subject>Motor Neurons - pathology</subject><subject>Notch</subject><subject>Phenotype</subject><subject>Protein Transport</subject><subject>Receptors, Notch - metabolism</subject><subject>Signal Transduction</subject><subject>Tissue growth</subject><issn>0925-4773</issn><issn>1872-6356</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtLAzEUhYMoWh8_wI3MTjdT854EQRSfhaIb9yFNMm3KNKmTmaL_3tSq6EYIXJL73cPNOQAcIzhEEPHz-XAR7RDDz_sQQrQFBkhUuOSE8W0wgBKzklYV2QP7Kc1hJhBHu2API8gY5XQAru6CjQ-jIgv1je5cKp5iZ2ZF8tOgGx-mhQ620G8xFNPeWx2MK3wobtuY4nLmG30IdmrdJHf0VQ_Ay_3dy81jOX5-GN1cj0tDBelKbq1lUHKna2ytRpgTNJFUkmqChbRauIpQjEnNBa5YLdGEU2mEFlBSggw5AJcb2WU_WThrXOha3ahl6xe6fVdRe_W3E_xMTeNKEUhkPlng9Eugja-9S51a-GRc0-jgYp-UYKiiFWM8k2f_kghCkZeUcI2iDWqyH6l19c9CCKp1RGqusrNqHdH6KQeQZ05-_-Rn4juTDFxsAJftXHnXqmS8y8Zb3zrTKRv9P_IfDLeg3A</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>O’Keefe, David D.</creator><creator>Edgar, Bruce A.</creator><creator>Saucedo, Leslie J.</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>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110101</creationdate><title>EndoGI modulates Notch signaling and axon guidance in Drosophila</title><author>O’Keefe, David D. ; Edgar, Bruce A. ; Saucedo, Leslie J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-6ddd5096eaf2dda12631b94937b289da8e734223f68275f91b649c8a809431c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Axon guidance</topic><topic>Axons - metabolism</topic><topic>Axons - pathology</topic><topic>Delta</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - embryology</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila melanogaster - ultrastructure</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Embryo, Nonmammalian - pathology</topic><topic>EndoGI</topic><topic>Eye - growth &amp; development</topic><topic>Eye - ultrastructure</topic><topic>Female</topic><topic>Genes, Insect - genetics</topic><topic>Motor neuron</topic><topic>Motor Neurons - metabolism</topic><topic>Motor Neurons - pathology</topic><topic>Notch</topic><topic>Phenotype</topic><topic>Protein Transport</topic><topic>Receptors, Notch - metabolism</topic><topic>Signal Transduction</topic><topic>Tissue growth</topic><toplevel>online_resources</toplevel><creatorcontrib>O’Keefe, David D.</creatorcontrib><creatorcontrib>Edgar, Bruce A.</creatorcontrib><creatorcontrib>Saucedo, Leslie J.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Mechanisms of development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O’Keefe, David D.</au><au>Edgar, Bruce A.</au><au>Saucedo, Leslie J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EndoGI modulates Notch signaling and axon guidance in Drosophila</atitle><jtitle>Mechanisms of development</jtitle><addtitle>Mech Dev</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>128</volume><issue>1</issue><spage>59</spage><epage>70</epage><pages>59-70</pages><issn>0925-4773</issn><eissn>1872-6356</eissn><abstract>Signaling through the Notch receptor has dramatically different effects depending on cell type and developmental timing. While a myriad of biological systems affected by Notch have been described, the molecular mechanisms by which a generic Notch signal is translated into a cell-type-specific output are less clear. Canonically, the Notch intracellular domain (NICD) translocates into the nucleus upon ligand binding to transcriptionally regulate target genes. In order to generate specificity, therefore, additional factors must exist that modulate NICD activity. Here we describe a novel regulator of the Notch pathway, Endonuclease GI (EndoGI). EndoGI localizes to the nucleus of most cells and activates Notch signaling when overexpressed. In the absence of endoGI, mutant animals are viable, but uncoordinated as motor neurons fail to innervate their appropriate muscle targets. Our data is therefore consistent with EndoGI functioning as a positive regulator of the Notch signaling pathway, playing a critical role during axon guidance of motor neurons.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>21055464</pmid><doi>10.1016/j.mod.2010.10.001</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0925-4773
ispartof Mechanisms of development, 2011-01, Vol.128 (1), p.59-70
issn 0925-4773
1872-6356
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3039039
source MEDLINE; Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals
subjects Animals
Animals, Genetically Modified
Axon guidance
Axons - metabolism
Axons - pathology
Delta
Drosophila
Drosophila melanogaster - embryology
Drosophila melanogaster - genetics
Drosophila melanogaster - metabolism
Drosophila melanogaster - ultrastructure
Drosophila Proteins - genetics
Drosophila Proteins - metabolism
Embryo, Nonmammalian - metabolism
Embryo, Nonmammalian - pathology
EndoGI
Eye - growth & development
Eye - ultrastructure
Female
Genes, Insect - genetics
Motor neuron
Motor Neurons - metabolism
Motor Neurons - pathology
Notch
Phenotype
Protein Transport
Receptors, Notch - metabolism
Signal Transduction
Tissue growth
title EndoGI modulates Notch signaling and axon guidance in Drosophila
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T04%3A09%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=EndoGI%20modulates%20Notch%20signaling%20and%20axon%20guidance%20in%20Drosophila&rft.jtitle=Mechanisms%20of%20development&rft.au=O%E2%80%99Keefe,%20David%20D.&rft.date=2011-01-01&rft.volume=128&rft.issue=1&rft.spage=59&rft.epage=70&rft.pages=59-70&rft.issn=0925-4773&rft.eissn=1872-6356&rft_id=info:doi/10.1016/j.mod.2010.10.001&rft_dat=%3Cproquest_pubme%3E1008827906%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1008827906&rft_id=info:pmid/21055464&rft_els_id=S0925477310000808&rfr_iscdi=true