Expression of synaptotagmin in Drosophila reveals transport and localization of synaptic vesicles to the synapse
Synaptotagmin is a synaptic vesicle-specific integral membrane protein that has been suggested to play a key role in synaptic vesicle docking and fusion. By monitoring Synaptotagmin's cellular and subcellular distribution during development, it is possible to study synaptic vesicle localization...
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Veröffentlicht in: | Development (Cambridge) 1993-08, Vol.118 (4), p.1077-1088 |
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description | Synaptotagmin is a synaptic vesicle-specific integral membrane protein that has been suggested to play a key role in synaptic vesicle docking and fusion. By monitoring Synaptotagmin's cellular and subcellular distribution during development, it is possible to study synaptic vesicle localization and transport, and synapse formation. We have initiated the study of Synaptotagmin's expression during Drosophila neurogenesis in order to follow synaptic vesicle movement prior to and during synapse formation, as well as to localize synaptic sites in Drosophila. In situ hybridizations to whole-mount embryos show that synaptotagmin (syt) message is present in the cell bodies of all peripheral nervous system neurons and many, if not all, central nervous system neurons during neurite outgrowth and synapse formation, and in mature neurons. Immunocytochemical staining with antisera specific to Synaptotagmin indicates that the protein is present at all stages of the Drosophila life cycle following germ band retraction. In embryos, Synaptotagmin is only transiently localized to the cell body of neurons and is transported rapidly along axons during axonogenesis. After synapse formation, Synaptotagmin accumulates in a punctate pattern at all identifiable synaptic contact sites, suggesting a general role for Synaptotagmin in synapse function. In embryos and larvae, the most intense staining is found along two broad longitudinal tracts on the dorsal side of the ventral nerve cord and the brain, and at neuromuscular junctions in the periphery. In the adult head, Synaptotagmin localizes the discrete regions of the neurophil where synapses are predicted to occur. These data indicate that synaptic vesicles are present in axons before synapse formation, and become restricted to synaptic contact sites after synapses are formed. Since a similar expression pattern of Synaptotagmin has been reported in mammals, we propose that the function of Synaptotagmin and the mechanisms governing localization of the synaptic vesicle before and after synapse formation are conserved in invertebrate and vertebrate species. The ability to mark synapses in Drosophila should facilitate the study of synapse formation and function, providing a new tool to dissect the molecular mechanisms underlying these processes. |
doi_str_mv | 10.1242/dev.118.4.1077 |
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T ; BELLEN, H. J ; PERIN, M. S</creator><creatorcontrib>LITTLETON, J. T ; BELLEN, H. J ; PERIN, M. S</creatorcontrib><description>Synaptotagmin is a synaptic vesicle-specific integral membrane protein that has been suggested to play a key role in synaptic vesicle docking and fusion. By monitoring Synaptotagmin's cellular and subcellular distribution during development, it is possible to study synaptic vesicle localization and transport, and synapse formation. We have initiated the study of Synaptotagmin's expression during Drosophila neurogenesis in order to follow synaptic vesicle movement prior to and during synapse formation, as well as to localize synaptic sites in Drosophila. In situ hybridizations to whole-mount embryos show that synaptotagmin (syt) message is present in the cell bodies of all peripheral nervous system neurons and many, if not all, central nervous system neurons during neurite outgrowth and synapse formation, and in mature neurons. Immunocytochemical staining with antisera specific to Synaptotagmin indicates that the protein is present at all stages of the Drosophila life cycle following germ band retraction. In embryos, Synaptotagmin is only transiently localized to the cell body of neurons and is transported rapidly along axons during axonogenesis. After synapse formation, Synaptotagmin accumulates in a punctate pattern at all identifiable synaptic contact sites, suggesting a general role for Synaptotagmin in synapse function. In embryos and larvae, the most intense staining is found along two broad longitudinal tracts on the dorsal side of the ventral nerve cord and the brain, and at neuromuscular junctions in the periphery. In the adult head, Synaptotagmin localizes the discrete regions of the neurophil where synapses are predicted to occur. These data indicate that synaptic vesicles are present in axons before synapse formation, and become restricted to synaptic contact sites after synapses are formed. Since a similar expression pattern of Synaptotagmin has been reported in mammals, we propose that the function of Synaptotagmin and the mechanisms governing localization of the synaptic vesicle before and after synapse formation are conserved in invertebrate and vertebrate species. The ability to mark synapses in Drosophila should facilitate the study of synapse formation and function, providing a new tool to dissect the molecular mechanisms underlying these processes.</description><identifier>ISSN: 0950-1991</identifier><identifier>EISSN: 1477-9129</identifier><identifier>DOI: 10.1242/dev.118.4.1077</identifier><identifier>PMID: 8269841</identifier><language>eng</language><publisher>Cambridge: The Company of Biologists Limited</publisher><subject>Animals ; Biochemistry. Physiology. Immunology ; Biological and medical sciences ; Calcium-Binding Proteins ; Drosophila ; Drosophila - embryology ; Drosophila - genetics ; Fundamental and applied biological sciences. Psychology ; Gene Expression - physiology ; Genes, Insect - genetics ; Immunoblotting ; Immunohistochemistry ; In Situ Hybridization ; Insecta ; Invertebrates ; Membrane Glycoproteins - analysis ; Membrane Glycoproteins - genetics ; Nerve Tissue Proteins - analysis ; Nerve Tissue Proteins - genetics ; Nervous System - embryology ; Neuromuscular Junction - chemistry ; Physiology. Development ; Synapses - chemistry ; Synapses - physiology ; Synaptic Vesicles - chemistry ; Synaptic Vesicles - physiology ; Synaptotagmins</subject><ispartof>Development (Cambridge), 1993-08, Vol.118 (4), p.1077-1088</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-b207b6447e7250563c16aca48016af05d2866be769e7c1cb1a83f8d82ca461bb3</citedby><cites>FETCH-LOGICAL-c454t-b207b6447e7250563c16aca48016af05d2866be769e7c1cb1a83f8d82ca461bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3665,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3803652$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8269841$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LITTLETON, J. T</creatorcontrib><creatorcontrib>BELLEN, H. J</creatorcontrib><creatorcontrib>PERIN, M. S</creatorcontrib><title>Expression of synaptotagmin in Drosophila reveals transport and localization of synaptic vesicles to the synapse</title><title>Development (Cambridge)</title><addtitle>Development</addtitle><description>Synaptotagmin is a synaptic vesicle-specific integral membrane protein that has been suggested to play a key role in synaptic vesicle docking and fusion. By monitoring Synaptotagmin's cellular and subcellular distribution during development, it is possible to study synaptic vesicle localization and transport, and synapse formation. We have initiated the study of Synaptotagmin's expression during Drosophila neurogenesis in order to follow synaptic vesicle movement prior to and during synapse formation, as well as to localize synaptic sites in Drosophila. In situ hybridizations to whole-mount embryos show that synaptotagmin (syt) message is present in the cell bodies of all peripheral nervous system neurons and many, if not all, central nervous system neurons during neurite outgrowth and synapse formation, and in mature neurons. Immunocytochemical staining with antisera specific to Synaptotagmin indicates that the protein is present at all stages of the Drosophila life cycle following germ band retraction. In embryos, Synaptotagmin is only transiently localized to the cell body of neurons and is transported rapidly along axons during axonogenesis. After synapse formation, Synaptotagmin accumulates in a punctate pattern at all identifiable synaptic contact sites, suggesting a general role for Synaptotagmin in synapse function. In embryos and larvae, the most intense staining is found along two broad longitudinal tracts on the dorsal side of the ventral nerve cord and the brain, and at neuromuscular junctions in the periphery. In the adult head, Synaptotagmin localizes the discrete regions of the neurophil where synapses are predicted to occur. These data indicate that synaptic vesicles are present in axons before synapse formation, and become restricted to synaptic contact sites after synapses are formed. Since a similar expression pattern of Synaptotagmin has been reported in mammals, we propose that the function of Synaptotagmin and the mechanisms governing localization of the synaptic vesicle before and after synapse formation are conserved in invertebrate and vertebrate species. The ability to mark synapses in Drosophila should facilitate the study of synapse formation and function, providing a new tool to dissect the molecular mechanisms underlying these processes.</description><subject>Animals</subject><subject>Biochemistry. Physiology. Immunology</subject><subject>Biological and medical sciences</subject><subject>Calcium-Binding Proteins</subject><subject>Drosophila</subject><subject>Drosophila - embryology</subject><subject>Drosophila - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression - physiology</subject><subject>Genes, Insect - genetics</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Insecta</subject><subject>Invertebrates</subject><subject>Membrane Glycoproteins - analysis</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Nerve Tissue Proteins - analysis</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nervous System - embryology</subject><subject>Neuromuscular Junction - chemistry</subject><subject>Physiology. Development</subject><subject>Synapses - chemistry</subject><subject>Synapses - physiology</subject><subject>Synaptic Vesicles - chemistry</subject><subject>Synaptic Vesicles - physiology</subject><subject>Synaptotagmins</subject><issn>0950-1991</issn><issn>1477-9129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS0EKtuFKzekHBC3BNtxbOeISvmQKvXSni3HmewaeePg8S4tf3292lUFJyRr5vB-fiO9R8g7RhvGBf80wqFhTDeiYVSpF2TFhFJ1z3j_kqxo39Ga9T17TS4Rf1JKW6nUBbnQXPZasBVZrh-WBIg-zlWcKnyc7ZJjtpudn6vyvqSIcdn6YKsEB7ABq5zsjEtMubLzWIXobPB_bP7HwbvqAOhdgMLHKm_hJCC8Ia-m4gJvz3tN7r9e3119r29uv_24-nxTO9GJXA-cqkEKoUDxjnaydUxaZ4WmZU-0G7mWcgAle1COuYFZ3U561Lwwkg1DuyYfT75Lir_2gNnsPDoIwc4Q92iUZK1qy_gfyKTkSpXk1qQ5ga5kggkmsyS_s-nRMGqOXZjShSldGGGOXZQP78_O-2EH4zN-Dr_oH866xRLiVHJ1Hp-xVpe2Ol6w-oRt_Wb72ycwg48hbjxmPJ6EEJe_zz4BHPaj7A</recordid><startdate>19930801</startdate><enddate>19930801</enddate><creator>LITTLETON, J. T</creator><creator>BELLEN, H. J</creator><creator>PERIN, M. S</creator><general>The Company of Biologists Limited</general><general>Company of Biologists</general><scope>IQODW</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>7SS</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19930801</creationdate><title>Expression of synaptotagmin in Drosophila reveals transport and localization of synaptic vesicles to the synapse</title><author>LITTLETON, J. T ; BELLEN, H. J ; PERIN, M. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-b207b6447e7250563c16aca48016af05d2866be769e7c1cb1a83f8d82ca461bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Biochemistry. Physiology. Immunology</topic><topic>Biological and medical sciences</topic><topic>Calcium-Binding Proteins</topic><topic>Drosophila</topic><topic>Drosophila - embryology</topic><topic>Drosophila - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression - physiology</topic><topic>Genes, Insect - genetics</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>Insecta</topic><topic>Invertebrates</topic><topic>Membrane Glycoproteins - analysis</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Nerve Tissue Proteins - analysis</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nervous System - embryology</topic><topic>Neuromuscular Junction - chemistry</topic><topic>Physiology. Development</topic><topic>Synapses - chemistry</topic><topic>Synapses - physiology</topic><topic>Synaptic Vesicles - chemistry</topic><topic>Synaptic Vesicles - physiology</topic><topic>Synaptotagmins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LITTLETON, J. T</creatorcontrib><creatorcontrib>BELLEN, H. J</creatorcontrib><creatorcontrib>PERIN, M. 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S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of synaptotagmin in Drosophila reveals transport and localization of synaptic vesicles to the synapse</atitle><jtitle>Development (Cambridge)</jtitle><addtitle>Development</addtitle><date>1993-08-01</date><risdate>1993</risdate><volume>118</volume><issue>4</issue><spage>1077</spage><epage>1088</epage><pages>1077-1088</pages><issn>0950-1991</issn><eissn>1477-9129</eissn><abstract>Synaptotagmin is a synaptic vesicle-specific integral membrane protein that has been suggested to play a key role in synaptic vesicle docking and fusion. By monitoring Synaptotagmin's cellular and subcellular distribution during development, it is possible to study synaptic vesicle localization and transport, and synapse formation. We have initiated the study of Synaptotagmin's expression during Drosophila neurogenesis in order to follow synaptic vesicle movement prior to and during synapse formation, as well as to localize synaptic sites in Drosophila. In situ hybridizations to whole-mount embryos show that synaptotagmin (syt) message is present in the cell bodies of all peripheral nervous system neurons and many, if not all, central nervous system neurons during neurite outgrowth and synapse formation, and in mature neurons. Immunocytochemical staining with antisera specific to Synaptotagmin indicates that the protein is present at all stages of the Drosophila life cycle following germ band retraction. In embryos, Synaptotagmin is only transiently localized to the cell body of neurons and is transported rapidly along axons during axonogenesis. After synapse formation, Synaptotagmin accumulates in a punctate pattern at all identifiable synaptic contact sites, suggesting a general role for Synaptotagmin in synapse function. In embryos and larvae, the most intense staining is found along two broad longitudinal tracts on the dorsal side of the ventral nerve cord and the brain, and at neuromuscular junctions in the periphery. In the adult head, Synaptotagmin localizes the discrete regions of the neurophil where synapses are predicted to occur. These data indicate that synaptic vesicles are present in axons before synapse formation, and become restricted to synaptic contact sites after synapses are formed. Since a similar expression pattern of Synaptotagmin has been reported in mammals, we propose that the function of Synaptotagmin and the mechanisms governing localization of the synaptic vesicle before and after synapse formation are conserved in invertebrate and vertebrate species. The ability to mark synapses in Drosophila should facilitate the study of synapse formation and function, providing a new tool to dissect the molecular mechanisms underlying these processes.</abstract><cop>Cambridge</cop><pub>The Company of Biologists Limited</pub><pmid>8269841</pmid><doi>10.1242/dev.118.4.1077</doi><tpages>12</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Company of Biologists |
subjects | Animals Biochemistry. Physiology. Immunology Biological and medical sciences Calcium-Binding Proteins Drosophila Drosophila - embryology Drosophila - genetics Fundamental and applied biological sciences. Psychology Gene Expression - physiology Genes, Insect - genetics Immunoblotting Immunohistochemistry In Situ Hybridization Insecta Invertebrates Membrane Glycoproteins - analysis Membrane Glycoproteins - genetics Nerve Tissue Proteins - analysis Nerve Tissue Proteins - genetics Nervous System - embryology Neuromuscular Junction - chemistry Physiology. Development Synapses - chemistry Synapses - physiology Synaptic Vesicles - chemistry Synaptic Vesicles - physiology Synaptotagmins |
title | Expression of synaptotagmin in Drosophila reveals transport and localization of synaptic vesicles to the synapse |
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