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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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.
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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. 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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 &amp; development</subject><subject>Ectoderm</subject><subject>Embryo, Nonmammalian</subject><subject>Embryonic Development - genetics</subject><subject>Embryos</subject><subject>Endoderm</subject><subject>Endoderm - growth &amp; 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 &amp; 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 &amp; development</topic><topic>Ectoderm</topic><topic>Embryo, Nonmammalian</topic><topic>Embryonic Development - genetics</topic><topic>Embryos</topic><topic>Endoderm</topic><topic>Endoderm - growth &amp; 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 &amp; 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 &amp; 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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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