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Genotype-Phenotype Associations in a Nonmodel Prokaryote
To help define the biological functions of nonessential genes of Francisella novicida, we measured the growth of arrayed members of a comprehensive transposon mutant library under a variety of nutrition and stress conditions. Mutant phenotypes were identified for 37% of the genes, corresponding to t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312209/ https://www.ncbi.nlm.nih.gov/pubmed/22434848 http://dx.doi.org/10.1128/mBio.00001-12 |
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author | Enstrom, Mark Held, Kiara Ramage, Beth Brittnacher, Mitchell Gallagher, Larry Manoil, Colin |
author_facet | Enstrom, Mark Held, Kiara Ramage, Beth Brittnacher, Mitchell Gallagher, Larry Manoil, Colin |
author_sort | Enstrom, Mark |
collection | PubMed |
description | To help define the biological functions of nonessential genes of Francisella novicida, we measured the growth of arrayed members of a comprehensive transposon mutant library under a variety of nutrition and stress conditions. Mutant phenotypes were identified for 37% of the genes, corresponding to ten carbon source utilization pathways, nine amino acid- and nucleotide-biosynthetic pathways, ten intrinsic antibiotic resistance traits, and six other stress resistance traits. The greatest surprise of the analysis was the large number of genotype-phenotype relationships that were not predictable from studies of Escherichia coli and other model species. The study identified candidate genes for a missing glycolysis function (phosphofructokinase), an unusual proline-biosynthetic pathway, parallel outer membrane lipid asymmetry maintenance systems, and novel antibiotic resistance functions. The analysis provides an evaluation of annotation predictions, identifies cases in which fundamental processes differ from those in model species, and helps create an empirical foundation for understanding virulence and other complex processes. |
format | Online Article Text |
id | pubmed-3312209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-33122092012-03-26 Genotype-Phenotype Associations in a Nonmodel Prokaryote Enstrom, Mark Held, Kiara Ramage, Beth Brittnacher, Mitchell Gallagher, Larry Manoil, Colin mBio Research Article To help define the biological functions of nonessential genes of Francisella novicida, we measured the growth of arrayed members of a comprehensive transposon mutant library under a variety of nutrition and stress conditions. Mutant phenotypes were identified for 37% of the genes, corresponding to ten carbon source utilization pathways, nine amino acid- and nucleotide-biosynthetic pathways, ten intrinsic antibiotic resistance traits, and six other stress resistance traits. The greatest surprise of the analysis was the large number of genotype-phenotype relationships that were not predictable from studies of Escherichia coli and other model species. The study identified candidate genes for a missing glycolysis function (phosphofructokinase), an unusual proline-biosynthetic pathway, parallel outer membrane lipid asymmetry maintenance systems, and novel antibiotic resistance functions. The analysis provides an evaluation of annotation predictions, identifies cases in which fundamental processes differ from those in model species, and helps create an empirical foundation for understanding virulence and other complex processes. American Society of Microbiology 2012-03-20 /pmc/articles/PMC3312209/ /pubmed/22434848 http://dx.doi.org/10.1128/mBio.00001-12 Text en Copyright © 2012 Enstrom et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Enstrom, Mark Held, Kiara Ramage, Beth Brittnacher, Mitchell Gallagher, Larry Manoil, Colin Genotype-Phenotype Associations in a Nonmodel Prokaryote |
title | Genotype-Phenotype Associations in a Nonmodel Prokaryote |
title_full | Genotype-Phenotype Associations in a Nonmodel Prokaryote |
title_fullStr | Genotype-Phenotype Associations in a Nonmodel Prokaryote |
title_full_unstemmed | Genotype-Phenotype Associations in a Nonmodel Prokaryote |
title_short | Genotype-Phenotype Associations in a Nonmodel Prokaryote |
title_sort | genotype-phenotype associations in a nonmodel prokaryote |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312209/ https://www.ncbi.nlm.nih.gov/pubmed/22434848 http://dx.doi.org/10.1128/mBio.00001-12 |
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