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The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination
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...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Genetics Society of America
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054018/ https://www.ncbi.nlm.nih.gov/pubmed/32132154 http://dx.doi.org/10.1534/genetics.119.301292 |
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author | Martin, Adam C. |
author_facet | Martin, Adam C. |
author_sort | Martin, Adam C. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7054018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-70540182020-03-11 The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination Martin, Adam C. Genetics Flybook 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. Genetics Society of America 2020-03 2019-12-11 /pmc/articles/PMC7054018/ /pubmed/32132154 http://dx.doi.org/10.1534/genetics.119.301292 Text en Copyright © 2020 Martin Available freely online through the author-supported open access option. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Flybook Martin, Adam C. The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
title | The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
title_full | The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
title_fullStr | The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
title_full_unstemmed | The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
title_short | The Physical Mechanisms of Drosophila Gastrulation: Mesoderm and Endoderm Invagination |
title_sort | physical mechanisms of drosophila gastrulation: mesoderm and endoderm invagination |
topic | Flybook |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054018/ https://www.ncbi.nlm.nih.gov/pubmed/32132154 http://dx.doi.org/10.1534/genetics.119.301292 |
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