Genotype-Phenotype Associations in a Nonmodel Prokaryote

ABSTRACT 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, correspon...

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Autores principales: Mark Enstrom, Kiara Held, Beth Ramage, Mitchell Brittnacher, Larry Gallagher, Colin Manoil
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Lenguaje:EN
Publicado: American Society for Microbiology 2012
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spelling oai:doaj.org-article:ccf55f3555474e7d86cf56ddf7f620ea2021-11-15T15:39:08ZGenotype-Phenotype Associations in a Nonmodel Prokaryote10.1128/mBio.00001-122150-7511https://doaj.org/article/ccf55f3555474e7d86cf56ddf7f620ea2012-05-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.00001-12https://doaj.org/toc/2150-7511ABSTRACT 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. IMPORTANCE The value of genome sequences as foundations for analyzing complex traits in nonmodel organisms is limited by the need to rely almost exclusively on sequence similarities to predict gene functions in annotations. Many genes cannot be assigned functions, and some predictions are incorrect or incomplete. Due to these limitations, genome-scale experimental approaches that test and extend bioinformatics-based predictions are sorely needed. In this study, we describe such an approach based on phenotypic analysis of a comprehensive, sequence-defined transposon mutant library.Mark EnstromKiara HeldBeth RamageMitchell BrittnacherLarry GallagherColin ManoilAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 3, Iss 2 (2012)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Mark Enstrom
Kiara Held
Beth Ramage
Mitchell Brittnacher
Larry Gallagher
Colin Manoil
Genotype-Phenotype Associations in a Nonmodel Prokaryote
description ABSTRACT 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. IMPORTANCE The value of genome sequences as foundations for analyzing complex traits in nonmodel organisms is limited by the need to rely almost exclusively on sequence similarities to predict gene functions in annotations. Many genes cannot be assigned functions, and some predictions are incorrect or incomplete. Due to these limitations, genome-scale experimental approaches that test and extend bioinformatics-based predictions are sorely needed. In this study, we describe such an approach based on phenotypic analysis of a comprehensive, sequence-defined transposon mutant library.
format article
author Mark Enstrom
Kiara Held
Beth Ramage
Mitchell Brittnacher
Larry Gallagher
Colin Manoil
author_facet Mark Enstrom
Kiara Held
Beth Ramage
Mitchell Brittnacher
Larry Gallagher
Colin Manoil
author_sort Mark Enstrom
title Genotype-Phenotype Associations in a Nonmodel Prokaryote
title_short 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_sort genotype-phenotype associations in a nonmodel prokaryote
publisher American Society for Microbiology
publishDate 2012
url https://doaj.org/article/ccf55f3555474e7d86cf56ddf7f620ea
work_keys_str_mv AT markenstrom genotypephenotypeassociationsinanonmodelprokaryote
AT kiaraheld genotypephenotypeassociationsinanonmodelprokaryote
AT bethramage genotypephenotypeassociationsinanonmodelprokaryote
AT mitchellbrittnacher genotypephenotypeassociationsinanonmodelprokaryote
AT larrygallagher genotypephenotypeassociationsinanonmodelprokaryote
AT colinmanoil genotypephenotypeassociationsinanonmodelprokaryote
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