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Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita
The segmentation gene network in insects can produce equivalent phenotypic outputs despite differences in upstream regulatory inputs between species. We investigate the mechanistic basis of this phenomenon through a systems-level analysis of the gap gene network in the scuttle fly Megaselia abdita (...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337606/ https://www.ncbi.nlm.nih.gov/pubmed/25560971 http://dx.doi.org/10.7554/eLife.04785 |
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author | Wotton, Karl R Jiménez-Guri, Eva Crombach, Anton Janssens, Hilde Alcaine-Colet, Anna Lemke, Steffen Schmidt-Ott, Urs Jaeger, Johannes |
author_facet | Wotton, Karl R Jiménez-Guri, Eva Crombach, Anton Janssens, Hilde Alcaine-Colet, Anna Lemke, Steffen Schmidt-Ott, Urs Jaeger, Johannes |
author_sort | Wotton, Karl R |
collection | PubMed |
description | The segmentation gene network in insects can produce equivalent phenotypic outputs despite differences in upstream regulatory inputs between species. We investigate the mechanistic basis of this phenomenon through a systems-level analysis of the gap gene network in the scuttle fly Megaselia abdita (Phoridae). It combines quantification of gene expression at high spatio-temporal resolution with systematic knock-downs by RNA interference (RNAi). Initiation and dynamics of gap gene expression differ markedly between M. abdita and Drosophila melanogaster, while the output of the system converges to equivalent patterns at the end of the blastoderm stage. Although the qualitative structure of the gap gene network is conserved, there are differences in the strength of regulatory interactions between species. We term such network rewiring ‘quantitative system drift’. It provides a mechanistic explanation for the developmental hourglass model in the dipteran lineage. Quantitative system drift is likely to be a widespread mechanism for developmental evolution. DOI: http://dx.doi.org/10.7554/eLife.04785.001 |
format | Online Article Text |
id | pubmed-4337606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43376062015-03-04 Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita Wotton, Karl R Jiménez-Guri, Eva Crombach, Anton Janssens, Hilde Alcaine-Colet, Anna Lemke, Steffen Schmidt-Ott, Urs Jaeger, Johannes eLife Developmental Biology and Stem Cells The segmentation gene network in insects can produce equivalent phenotypic outputs despite differences in upstream regulatory inputs between species. We investigate the mechanistic basis of this phenomenon through a systems-level analysis of the gap gene network in the scuttle fly Megaselia abdita (Phoridae). It combines quantification of gene expression at high spatio-temporal resolution with systematic knock-downs by RNA interference (RNAi). Initiation and dynamics of gap gene expression differ markedly between M. abdita and Drosophila melanogaster, while the output of the system converges to equivalent patterns at the end of the blastoderm stage. Although the qualitative structure of the gap gene network is conserved, there are differences in the strength of regulatory interactions between species. We term such network rewiring ‘quantitative system drift’. It provides a mechanistic explanation for the developmental hourglass model in the dipteran lineage. Quantitative system drift is likely to be a widespread mechanism for developmental evolution. DOI: http://dx.doi.org/10.7554/eLife.04785.001 eLife Sciences Publications, Ltd 2015-01-05 /pmc/articles/PMC4337606/ /pubmed/25560971 http://dx.doi.org/10.7554/eLife.04785 Text en © 2015, Wotton et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Wotton, Karl R Jiménez-Guri, Eva Crombach, Anton Janssens, Hilde Alcaine-Colet, Anna Lemke, Steffen Schmidt-Ott, Urs Jaeger, Johannes Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita |
title | Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita |
title_full | Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita |
title_fullStr | Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita |
title_full_unstemmed | Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita |
title_short | Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita |
title_sort | quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly megaselia abdita |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337606/ https://www.ncbi.nlm.nih.gov/pubmed/25560971 http://dx.doi.org/10.7554/eLife.04785 |
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