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Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa

Classical forward genetics has been foundational to modern biology, and has been the paradigm for characterizing the role of genes in shaping phenotypes for decades. In recent years, reverse genetics has been used to identify the functions of genes, via the intentional introduction of variation and...

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Autores principales: McCluskey, Kevin, Wiest, Aric E., Grigoriev, Igor V., Lipzen, Anna, Martin, Joel, Schackwitz, Wendy, Baker, Scott E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276140/
https://www.ncbi.nlm.nih.gov/pubmed/22384341
http://dx.doi.org/10.1534/g3.111.000307
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author McCluskey, Kevin
Wiest, Aric E.
Grigoriev, Igor V.
Lipzen, Anna
Martin, Joel
Schackwitz, Wendy
Baker, Scott E.
author_facet McCluskey, Kevin
Wiest, Aric E.
Grigoriev, Igor V.
Lipzen, Anna
Martin, Joel
Schackwitz, Wendy
Baker, Scott E.
author_sort McCluskey, Kevin
collection PubMed
description Classical forward genetics has been foundational to modern biology, and has been the paradigm for characterizing the role of genes in shaping phenotypes for decades. In recent years, reverse genetics has been used to identify the functions of genes, via the intentional introduction of variation and subsequent evaluation in physiological, molecular, and even population contexts. These approaches are complementary and whole genome analysis serves as a bridge between the two. We report in this article the whole genome sequencing of eighteen classical mutant strains of Neurospora crassa and the putative identification of the mutations associated with corresponding mutant phenotypes. Although some strains carry multiple unique nonsynonymous, nonsense, or frameshift mutations, the combined power of limiting the scope of the search based on genetic markers and of using a comparative analysis among the eighteen genomes provides strong support for the association between mutation and phenotype. For ten of the mutants, the mutant phenotype is recapitulated in classical or gene deletion mutants in Neurospora or other filamentous fungi. From thirteen to 137 nonsense mutations are present in each strain and indel sizes are shown to be highly skewed in gene coding sequence. Significant additional genetic variation was found in the eighteen mutant strains, and this variability defines multiple alleles of many genes. These alleles may be useful in further genetic and molecular analysis of known and yet-to-be-discovered functions and they invite new interpretations of molecular and genetic interactions in classical mutant strains.
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spelling pubmed-32761402012-03-01 Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa McCluskey, Kevin Wiest, Aric E. Grigoriev, Igor V. Lipzen, Anna Martin, Joel Schackwitz, Wendy Baker, Scott E. G3 (Bethesda) Investigation Classical forward genetics has been foundational to modern biology, and has been the paradigm for characterizing the role of genes in shaping phenotypes for decades. In recent years, reverse genetics has been used to identify the functions of genes, via the intentional introduction of variation and subsequent evaluation in physiological, molecular, and even population contexts. These approaches are complementary and whole genome analysis serves as a bridge between the two. We report in this article the whole genome sequencing of eighteen classical mutant strains of Neurospora crassa and the putative identification of the mutations associated with corresponding mutant phenotypes. Although some strains carry multiple unique nonsynonymous, nonsense, or frameshift mutations, the combined power of limiting the scope of the search based on genetic markers and of using a comparative analysis among the eighteen genomes provides strong support for the association between mutation and phenotype. For ten of the mutants, the mutant phenotype is recapitulated in classical or gene deletion mutants in Neurospora or other filamentous fungi. From thirteen to 137 nonsense mutations are present in each strain and indel sizes are shown to be highly skewed in gene coding sequence. Significant additional genetic variation was found in the eighteen mutant strains, and this variability defines multiple alleles of many genes. These alleles may be useful in further genetic and molecular analysis of known and yet-to-be-discovered functions and they invite new interpretations of molecular and genetic interactions in classical mutant strains. Genetics Society of America 2011-09-01 /pmc/articles/PMC3276140/ /pubmed/22384341 http://dx.doi.org/10.1534/g3.111.000307 Text en Copyright © 2011 McCluskey et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
McCluskey, Kevin
Wiest, Aric E.
Grigoriev, Igor V.
Lipzen, Anna
Martin, Joel
Schackwitz, Wendy
Baker, Scott E.
Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa
title Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa
title_full Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa
title_fullStr Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa
title_full_unstemmed Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa
title_short Rediscovery by Whole Genome Sequencing: Classical Mutations and Genome Polymorphisms in Neurospora crassa
title_sort rediscovery by whole genome sequencing: classical mutations and genome polymorphisms in neurospora crassa
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276140/
https://www.ncbi.nlm.nih.gov/pubmed/22384341
http://dx.doi.org/10.1534/g3.111.000307
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