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Partial penetrance facilitates developmental evolution in bacteria

Development normally occurs similarly in all individuals within an isogenic population, but mutations often affect the fate of individual organisms differently1-4. This phenomenon, known as partial penetrance, has been observed in diverse developmental systems. However, it remains unclear how the un...

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Autores principales: Eldar, Avigdor, Chary, Vasant, Xenopoulos, Panagiotis, Fontes, Michelle E., Loson, Oliver C., Dworkin, Jonathan, Piggot, Patrick, Elowitz, Michael B.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716064/
https://www.ncbi.nlm.nih.gov/pubmed/19578359
http://dx.doi.org/10.1038/nature08150
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author Eldar, Avigdor
Chary, Vasant
Xenopoulos, Panagiotis
Fontes, Michelle E.
Loson, Oliver C.
Dworkin, Jonathan
Piggot, Patrick
Elowitz, Michael B.
author_facet Eldar, Avigdor
Chary, Vasant
Xenopoulos, Panagiotis
Fontes, Michelle E.
Loson, Oliver C.
Dworkin, Jonathan
Piggot, Patrick
Elowitz, Michael B.
author_sort Eldar, Avigdor
collection PubMed
description Development normally occurs similarly in all individuals within an isogenic population, but mutations often affect the fate of individual organisms differently1-4. This phenomenon, known as partial penetrance, has been observed in diverse developmental systems. However, it remains unclear how the underlying genetic network specifies the set of possible alternative fates and how the relative frequencies of these fates evolve5-8. Here, we identify a stochastic cell fate determination process that operates in Bacillus subtilis sporulation mutants and show how it allows genetic control of the penetrance of multiple fates. Mutations in an inter-compartmental signaling process generate a set of discrete alternative fates not observed in wild-type cells, including rare formation of two viable “twin” spores, rather than one within a single cell. By genetically modulating chromosome replication and septation, we could systematically tune the penetrance of each mutant fate. Furthermore, signaling and replication perturbations synergize to dramatically increase the penetrance of twin sporulation. These results suggest a potential pathway for developmental evolution between monosporulation and twin sporulation through states of intermediate twin penetrance. Furthermore, time-lapse microscopy of twin sporulation in wild-type Clostridium oceanicum showed a strong resemblance to twin sporulation in these B. subtilis mutants9,10. Together the results suggest that noise can facilitate developmental evolution by enabling the initial expression of discrete morphological traits at low penetrance, and allowing their stabilization by gradual adjustment of genetic parameters.
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spelling pubmed-27160642010-01-23 Partial penetrance facilitates developmental evolution in bacteria Eldar, Avigdor Chary, Vasant Xenopoulos, Panagiotis Fontes, Michelle E. Loson, Oliver C. Dworkin, Jonathan Piggot, Patrick Elowitz, Michael B. Nature Article Development normally occurs similarly in all individuals within an isogenic population, but mutations often affect the fate of individual organisms differently1-4. This phenomenon, known as partial penetrance, has been observed in diverse developmental systems. However, it remains unclear how the underlying genetic network specifies the set of possible alternative fates and how the relative frequencies of these fates evolve5-8. Here, we identify a stochastic cell fate determination process that operates in Bacillus subtilis sporulation mutants and show how it allows genetic control of the penetrance of multiple fates. Mutations in an inter-compartmental signaling process generate a set of discrete alternative fates not observed in wild-type cells, including rare formation of two viable “twin” spores, rather than one within a single cell. By genetically modulating chromosome replication and septation, we could systematically tune the penetrance of each mutant fate. Furthermore, signaling and replication perturbations synergize to dramatically increase the penetrance of twin sporulation. These results suggest a potential pathway for developmental evolution between monosporulation and twin sporulation through states of intermediate twin penetrance. Furthermore, time-lapse microscopy of twin sporulation in wild-type Clostridium oceanicum showed a strong resemblance to twin sporulation in these B. subtilis mutants9,10. Together the results suggest that noise can facilitate developmental evolution by enabling the initial expression of discrete morphological traits at low penetrance, and allowing their stabilization by gradual adjustment of genetic parameters. 2009-07-05 2009-07-23 /pmc/articles/PMC2716064/ /pubmed/19578359 http://dx.doi.org/10.1038/nature08150 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Eldar, Avigdor
Chary, Vasant
Xenopoulos, Panagiotis
Fontes, Michelle E.
Loson, Oliver C.
Dworkin, Jonathan
Piggot, Patrick
Elowitz, Michael B.
Partial penetrance facilitates developmental evolution in bacteria
title Partial penetrance facilitates developmental evolution in bacteria
title_full Partial penetrance facilitates developmental evolution in bacteria
title_fullStr Partial penetrance facilitates developmental evolution in bacteria
title_full_unstemmed Partial penetrance facilitates developmental evolution in bacteria
title_short Partial penetrance facilitates developmental evolution in bacteria
title_sort partial penetrance facilitates developmental evolution in bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716064/
https://www.ncbi.nlm.nih.gov/pubmed/19578359
http://dx.doi.org/10.1038/nature08150
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