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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 (...

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Autores principales: Wotton, Karl R, Jiménez-Guri, Eva, Crombach, Anton, Janssens, Hilde, Alcaine-Colet, Anna, Lemke, Steffen, Schmidt-Ott, Urs, Jaeger, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
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
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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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