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Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks
A common occurrence in metazoan development is the rise of multiple tissues/organs from a single uniform precursor field. One example is the anterior forebrain of vertebrates, which produces the eyes, hypothalamus, diencephalon, and telencephalon. Another instance is the Drosophila wing disc, which...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792024/ https://www.ncbi.nlm.nih.gov/pubmed/29351292 http://dx.doi.org/10.1371/journal.pgen.1007185 |
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author | Palliyil, Sneha Zhu, Jinjin Baker, Luke R. Neuman, Sarah D. Bashirullah, Arash Kumar, Justin P. |
author_facet | Palliyil, Sneha Zhu, Jinjin Baker, Luke R. Neuman, Sarah D. Bashirullah, Arash Kumar, Justin P. |
author_sort | Palliyil, Sneha |
collection | PubMed |
description | A common occurrence in metazoan development is the rise of multiple tissues/organs from a single uniform precursor field. One example is the anterior forebrain of vertebrates, which produces the eyes, hypothalamus, diencephalon, and telencephalon. Another instance is the Drosophila wing disc, which generates the adult wing blade, the hinge, and the thorax. Gene regulatory networks (GRNs) that are comprised of signaling pathways and batteries of transcription factors parcel the undifferentiated field into discrete territories. This simple model is challenged by two observations. First, many GRN members that are thought to control the fate of one organ are actually expressed throughout the entire precursor field at earlier points in development. Second, each GRN can simultaneously promote one of the possible fates choices while repressing the other alternatives. It is therefore unclear how GRNs function to allocate tissue fates if their members are uniformly expressed and competing with each other within the same populations of cells. We address this paradigm by studying fate specification in the Drosophila eye-antennal disc. The disc, which begins its development as a homogeneous precursor field, produces a number of adult structures including the compound eyes, the ocelli, the antennae, the maxillary palps, and the surrounding head epidermis. Several selector genes that control the fates of the eye and antenna, respectively, are first expressed throughout the entire eye-antennal disc. We show that during early stages, these genes are tasked with promoting the growth of the entire field. Upon segregation to distinct territories within the disc, each GRN continues to promote growth while taking on the additional roles of promoting distinct primary fates and repressing alternate fates. The timing of both expression pattern restriction and expansion of functional duties is an elemental requirement for allocating fates within a single field. |
format | Online Article Text |
id | pubmed-5792024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57920242018-02-09 Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks Palliyil, Sneha Zhu, Jinjin Baker, Luke R. Neuman, Sarah D. Bashirullah, Arash Kumar, Justin P. PLoS Genet Research Article A common occurrence in metazoan development is the rise of multiple tissues/organs from a single uniform precursor field. One example is the anterior forebrain of vertebrates, which produces the eyes, hypothalamus, diencephalon, and telencephalon. Another instance is the Drosophila wing disc, which generates the adult wing blade, the hinge, and the thorax. Gene regulatory networks (GRNs) that are comprised of signaling pathways and batteries of transcription factors parcel the undifferentiated field into discrete territories. This simple model is challenged by two observations. First, many GRN members that are thought to control the fate of one organ are actually expressed throughout the entire precursor field at earlier points in development. Second, each GRN can simultaneously promote one of the possible fates choices while repressing the other alternatives. It is therefore unclear how GRNs function to allocate tissue fates if their members are uniformly expressed and competing with each other within the same populations of cells. We address this paradigm by studying fate specification in the Drosophila eye-antennal disc. The disc, which begins its development as a homogeneous precursor field, produces a number of adult structures including the compound eyes, the ocelli, the antennae, the maxillary palps, and the surrounding head epidermis. Several selector genes that control the fates of the eye and antenna, respectively, are first expressed throughout the entire eye-antennal disc. We show that during early stages, these genes are tasked with promoting the growth of the entire field. Upon segregation to distinct territories within the disc, each GRN continues to promote growth while taking on the additional roles of promoting distinct primary fates and repressing alternate fates. The timing of both expression pattern restriction and expansion of functional duties is an elemental requirement for allocating fates within a single field. Public Library of Science 2018-01-19 /pmc/articles/PMC5792024/ /pubmed/29351292 http://dx.doi.org/10.1371/journal.pgen.1007185 Text en © 2018 Palliyil et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Palliyil, Sneha Zhu, Jinjin Baker, Luke R. Neuman, Sarah D. Bashirullah, Arash Kumar, Justin P. Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
title | Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
title_full | Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
title_fullStr | Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
title_full_unstemmed | Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
title_short | Allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
title_sort | allocation of distinct organ fates from a precursor field requires a shift in expression and function of gene regulatory networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792024/ https://www.ncbi.nlm.nih.gov/pubmed/29351292 http://dx.doi.org/10.1371/journal.pgen.1007185 |
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