The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination
Abstract A critical juncture in early development is the partitioning of cells that will adopt different fates into three germ layers: the ectoderm, the mesoderm, and the endoderm. This step is achieved through the internalization of specified cells from the outermost surface layer, through a proces...
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A critical juncture in early development is the partitioning of cells that will adopt different fates into three germ layers: the ectoderm, the mesoderm, and the endoderm. This step is achieved through the internalization of specified cells from the outermost surface layer, through a process called gastrulation. In Drosophila, gastrulation is achieved through cell shape changes (i.e., apical constriction) that change tissue curvature and lead to the folding of a surface epithelium. Folding of embryonic tissue results in mesoderm and endoderm invagination, not as individual cells, but as collective tissue units. The tractability of Drosophila as a model system is best exemplified by how much we know about Drosophila gastrulation, from the signals that pattern the embryo to the molecular components that generate force, and how these components are organized to promote cell and tissue shape changes. For mesoderm invagination, graded signaling by the morphogen, Spätzle, sets up a gradient in transcriptional activity that leads to the expression of a secreted ligand (Folded gastrulation) and a transmembrane protein (T48). Together with the GPCR Mist, which is expressed in the mesoderm, and the GPCR Smog, which is expressed uniformly, these signals activate heterotrimeric G-protein and small Rho-family G-protein signaling to promote apical contractility and changes in cell and tissue shape. A notable feature of this signaling pathway is its intricate organization in both space and time. At the cellular level, signaling components and the cytoskeleton exhibit striking polarity, not only along the apical–basal cell axis, but also within the apical domain. Furthermore, gene expression controls a highly choreographed chain of events, the dynamics of which are critical for primordium invagination; it does not simply throw the cytoskeletal “on” switch. Finally, studies of Drosophila gastrulation have provided insight into how global tissue mechanics and movements are intertwined as multiple tissues simultaneously change shape. Overall, these studies have contributed to the view that cells respond to forces that propagate over great distances, demonstrating that cellular decisions, and, ultimately, tissue shape changes, proceed by integrating cues across an entire embryo. |
doi_str_mv | 10.1534/genetics.119.301292 |
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A critical juncture in early development is the partitioning of cells that will adopt different fates into three germ layers: the ectoderm, the mesoderm, and the endoderm. This step is achieved through the internalization of specified cells from the outermost surface layer, through a process called gastrulation. In Drosophila, gastrulation is achieved through cell shape changes (i.e., apical constriction) that change tissue curvature and lead to the folding of a surface epithelium. Folding of embryonic tissue results in mesoderm and endoderm invagination, not as individual cells, but as collective tissue units. The tractability of Drosophila as a model system is best exemplified by how much we know about Drosophila gastrulation, from the signals that pattern the embryo to the molecular components that generate force, and how these components are organized to promote cell and tissue shape changes. For mesoderm invagination, graded signaling by the morphogen, Spätzle, sets up a gradient in transcriptional activity that leads to the expression of a secreted ligand (Folded gastrulation) and a transmembrane protein (T48). Together with the GPCR Mist, which is expressed in the mesoderm, and the GPCR Smog, which is expressed uniformly, these signals activate heterotrimeric G-protein and small Rho-family G-protein signaling to promote apical contractility and changes in cell and tissue shape. A notable feature of this signaling pathway is its intricate organization in both space and time. At the cellular level, signaling components and the cytoskeleton exhibit striking polarity, not only along the apical–basal cell axis, but also within the apical domain. Furthermore, gene expression controls a highly choreographed chain of events, the dynamics of which are critical for primordium invagination; it does not simply throw the cytoskeletal “on” switch. Finally, studies of Drosophila gastrulation have provided insight into how global tissue mechanics and movements are intertwined as multiple tissues simultaneously change shape. Overall, these studies have contributed to the view that cells respond to forces that propagate over great distances, demonstrating that cellular decisions, and, ultimately, tissue shape changes, proceed by integrating cues across an entire embryo.</description><identifier>ISSN: 1943-2631</identifier><identifier>ISSN: 0016-6731</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1534/genetics.119.301292</identifier><identifier>PMID: 32132154</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Cell size ; Contractility ; Cytoskeleton ; Drosophila ; Drosophila melanogaster - genetics ; Drosophila melanogaster - growth & development ; Ectoderm ; Embryo, Nonmammalian ; Embryonic Development - genetics ; Embryos ; Endoderm ; Endoderm - growth & development ; Epithelium ; Flybook ; Folding ; G protein-coupled receptors ; Gastrulation ; Gastrulation - genetics ; Gene expression ; Gene Expression Regulation, Developmental - genetics ; Genetics ; Heparan sulfate ; Insects ; Internalization ; Ligands ; Membrane Proteins - genetics ; Mesoderm ; Mesoderm - growth & development ; Morphogenesis ; Morphogenesis - genetics ; Organisms ; Physical Phenomena ; Polarity ; Proteins ; rho GTP-Binding Proteins - genetics ; Signal transduction ; Signal Transduction - genetics ; Signaling ; Smog ; Surface layers ; Tissues ; Transcription</subject><ispartof>Genetics (Austin), 2020-03, Vol.214 (3), p.543-560</ispartof><rights>Genetics 2020 2020</rights><rights>Copyright © 2020 Martin.</rights><rights>Copyright Genetics Society of America Mar 2020</rights><rights>Copyright © 2020 Martin 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-177b5b15430143f8121b9351555fcd5f7bdd39fe3e3c5d3945f4c9387edb53a03</citedby><cites>FETCH-LOGICAL-c427t-177b5b15430143f8121b9351555fcd5f7bdd39fe3e3c5d3945f4c9387edb53a03</cites><orcidid>0000-0001-8060-2607</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32132154$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martin, Adam C</creatorcontrib><title>The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>Abstract
A critical juncture in early development is the partitioning of cells that will adopt different fates into three germ layers: the ectoderm, the mesoderm, and the endoderm. This step is achieved through the internalization of specified cells from the outermost surface layer, through a process called gastrulation. In Drosophila, gastrulation is achieved through cell shape changes (i.e., apical constriction) that change tissue curvature and lead to the folding of a surface epithelium. Folding of embryonic tissue results in mesoderm and endoderm invagination, not as individual cells, but as collective tissue units. The tractability of Drosophila as a model system is best exemplified by how much we know about Drosophila gastrulation, from the signals that pattern the embryo to the molecular components that generate force, and how these components are organized to promote cell and tissue shape changes. For mesoderm invagination, graded signaling by the morphogen, Spätzle, sets up a gradient in transcriptional activity that leads to the expression of a secreted ligand (Folded gastrulation) and a transmembrane protein (T48). Together with the GPCR Mist, which is expressed in the mesoderm, and the GPCR Smog, which is expressed uniformly, these signals activate heterotrimeric G-protein and small Rho-family G-protein signaling to promote apical contractility and changes in cell and tissue shape. A notable feature of this signaling pathway is its intricate organization in both space and time. At the cellular level, signaling components and the cytoskeleton exhibit striking polarity, not only along the apical–basal cell axis, but also within the apical domain. Furthermore, gene expression controls a highly choreographed chain of events, the dynamics of which are critical for primordium invagination; it does not simply throw the cytoskeletal “on” switch. Finally, studies of Drosophila gastrulation have provided insight into how global tissue mechanics and movements are intertwined as multiple tissues simultaneously change shape. Overall, these studies have contributed to the view that cells respond to forces that propagate over great distances, demonstrating that cellular decisions, and, ultimately, tissue shape changes, proceed by integrating cues across an entire embryo.</description><subject>Animals</subject><subject>Cell size</subject><subject>Contractility</subject><subject>Cytoskeleton</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Ectoderm</subject><subject>Embryo, Nonmammalian</subject><subject>Embryonic Development - genetics</subject><subject>Embryos</subject><subject>Endoderm</subject><subject>Endoderm - growth & development</subject><subject>Epithelium</subject><subject>Flybook</subject><subject>Folding</subject><subject>G protein-coupled receptors</subject><subject>Gastrulation</subject><subject>Gastrulation - genetics</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Developmental - genetics</subject><subject>Genetics</subject><subject>Heparan sulfate</subject><subject>Insects</subject><subject>Internalization</subject><subject>Ligands</subject><subject>Membrane Proteins - genetics</subject><subject>Mesoderm</subject><subject>Mesoderm - growth & development</subject><subject>Morphogenesis</subject><subject>Morphogenesis - genetics</subject><subject>Organisms</subject><subject>Physical Phenomena</subject><subject>Polarity</subject><subject>Proteins</subject><subject>rho GTP-Binding Proteins - genetics</subject><subject>Signal transduction</subject><subject>Signal Transduction - genetics</subject><subject>Signaling</subject><subject>Smog</subject><subject>Surface layers</subject><subject>Tissues</subject><subject>Transcription</subject><issn>1943-2631</issn><issn>0016-6731</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkVFLwzAUhYMobk5_gSAFX3zZTJpmbXwQZM45mOjD9DWkabpmtMlM2sH-vZndhvokBHIv-e7h3BwALhEcIIKj24XUslbCDRCiAwxRSMMj0EU0wv1wiNHxj7oDzpxbQgiHlCSnoIND5A-JuuBjXsjgrdg4JXgZvEhRcK1c5QKTB4_WOLMqVMmDCXe1bUpeK6PvPOZMJm0VcJ0FY521zVSv-ULpb-YcnOS8dPJid_fA-9N4Pnruz14n09HDrC-iMK77KI5Tknoj3n6E8wSFKKWYIEJILjKSx2mWYZpLLLEgvopIHgmKk1hmKcEc4h64b3VXTVrJTEhdW16ylVUVtxtmuGK_X7Qq2MKsWQxJBFHiBW52AtZ8NtLVrFJOyLLkWprGsRDHKCEE0dij13_QpWms9uttqQTSJIRDT-GWEv73nJX5wQyCbJsb2-fGfG6szc1PXf3c4zCzD8oDgxYwzepfil-d-aWA</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Martin, Adam C</creator><general>Oxford University Press</general><general>Genetics Society of America</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>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8060-2607</orcidid></search><sort><creationdate>20200301</creationdate><title>The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination</title><author>Martin, Adam C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-177b5b15430143f8121b9351555fcd5f7bdd39fe3e3c5d3945f4c9387edb53a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cell size</topic><topic>Contractility</topic><topic>Cytoskeleton</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Ectoderm</topic><topic>Embryo, Nonmammalian</topic><topic>Embryonic Development - genetics</topic><topic>Embryos</topic><topic>Endoderm</topic><topic>Endoderm - growth & development</topic><topic>Epithelium</topic><topic>Flybook</topic><topic>Folding</topic><topic>G protein-coupled receptors</topic><topic>Gastrulation</topic><topic>Gastrulation - genetics</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Developmental - genetics</topic><topic>Genetics</topic><topic>Heparan sulfate</topic><topic>Insects</topic><topic>Internalization</topic><topic>Ligands</topic><topic>Membrane Proteins - genetics</topic><topic>Mesoderm</topic><topic>Mesoderm - growth & development</topic><topic>Morphogenesis</topic><topic>Morphogenesis - genetics</topic><topic>Organisms</topic><topic>Physical Phenomena</topic><topic>Polarity</topic><topic>Proteins</topic><topic>rho GTP-Binding Proteins - genetics</topic><topic>Signal transduction</topic><topic>Signal Transduction - genetics</topic><topic>Signaling</topic><topic>Smog</topic><topic>Surface layers</topic><topic>Tissues</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martin, Adam C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martin, Adam C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>214</volume><issue>3</issue><spage>543</spage><epage>560</epage><pages>543-560</pages><issn>1943-2631</issn><issn>0016-6731</issn><eissn>1943-2631</eissn><abstract>Abstract
A critical juncture in early development is the partitioning of cells that will adopt different fates into three germ layers: the ectoderm, the mesoderm, and the endoderm. This step is achieved through the internalization of specified cells from the outermost surface layer, through a process called gastrulation. In Drosophila, gastrulation is achieved through cell shape changes (i.e., apical constriction) that change tissue curvature and lead to the folding of a surface epithelium. Folding of embryonic tissue results in mesoderm and endoderm invagination, not as individual cells, but as collective tissue units. The tractability of Drosophila as a model system is best exemplified by how much we know about Drosophila gastrulation, from the signals that pattern the embryo to the molecular components that generate force, and how these components are organized to promote cell and tissue shape changes. For mesoderm invagination, graded signaling by the morphogen, Spätzle, sets up a gradient in transcriptional activity that leads to the expression of a secreted ligand (Folded gastrulation) and a transmembrane protein (T48). Together with the GPCR Mist, which is expressed in the mesoderm, and the GPCR Smog, which is expressed uniformly, these signals activate heterotrimeric G-protein and small Rho-family G-protein signaling to promote apical contractility and changes in cell and tissue shape. A notable feature of this signaling pathway is its intricate organization in both space and time. At the cellular level, signaling components and the cytoskeleton exhibit striking polarity, not only along the apical–basal cell axis, but also within the apical domain. Furthermore, gene expression controls a highly choreographed chain of events, the dynamics of which are critical for primordium invagination; it does not simply throw the cytoskeletal “on” switch. Finally, studies of Drosophila gastrulation have provided insight into how global tissue mechanics and movements are intertwined as multiple tissues simultaneously change shape. Overall, these studies have contributed to the view that cells respond to forces that propagate over great distances, demonstrating that cellular decisions, and, ultimately, tissue shape changes, proceed by integrating cues across an entire embryo.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>32132154</pmid><doi>10.1534/genetics.119.301292</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0001-8060-2607</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell size Contractility Cytoskeleton Drosophila Drosophila melanogaster - genetics Drosophila melanogaster - growth & development Ectoderm Embryo, Nonmammalian Embryonic Development - genetics Embryos Endoderm Endoderm - growth & development Epithelium Flybook Folding G protein-coupled receptors Gastrulation Gastrulation - genetics Gene expression Gene Expression Regulation, Developmental - genetics Genetics Heparan sulfate Insects Internalization Ligands Membrane Proteins - genetics Mesoderm Mesoderm - growth & development Morphogenesis Morphogenesis - genetics Organisms Physical Phenomena Polarity Proteins rho GTP-Binding Proteins - genetics Signal transduction Signal Transduction - genetics Signaling Smog Surface layers Tissues Transcription |
title | The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
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