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Mapping Challenging Mutations by Whole-Genome Sequencing

Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their...

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Autores principales: Smith, Harold E., Fabritius, Amy S., Jaramillo-Lambert, Aimee, Golden, Andy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4856081/
https://www.ncbi.nlm.nih.gov/pubmed/26945029
http://dx.doi.org/10.1534/g3.116.028316
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author Smith, Harold E.
Fabritius, Amy S.
Jaramillo-Lambert, Aimee
Golden, Andy
author_facet Smith, Harold E.
Fabritius, Amy S.
Jaramillo-Lambert, Aimee
Golden, Andy
author_sort Smith, Harold E.
collection PubMed
description Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their genetic tractability. Therefore, most of the mapping methods for mutation identification by whole-genome sequencing are directed toward alleles that fulfill those criteria (i.e., single-gene, homozygous variants). However, such approaches are not entirely suitable for the characterization of a variety of more challenging mutations, such as dominant and semidominant alleles or multigenic traits. Therefore, we have developed strategies for the identification of those classes of mutations, using polymorphism mapping in Caenorhabditis elegans as our model for validation. We also report an alternative approach for mutation identification from traditional recombinant crosses, and a solution to the technical challenge of sequencing sterile or terminally arrested strains where population size is limiting. The methods described herein extend the applicability of whole-genome sequencing to a broader spectrum of mutations, including classes that are difficult to map by traditional means.
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spelling pubmed-48560812016-05-05 Mapping Challenging Mutations by Whole-Genome Sequencing Smith, Harold E. Fabritius, Amy S. Jaramillo-Lambert, Aimee Golden, Andy G3 (Bethesda) Investigations Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their genetic tractability. Therefore, most of the mapping methods for mutation identification by whole-genome sequencing are directed toward alleles that fulfill those criteria (i.e., single-gene, homozygous variants). However, such approaches are not entirely suitable for the characterization of a variety of more challenging mutations, such as dominant and semidominant alleles or multigenic traits. Therefore, we have developed strategies for the identification of those classes of mutations, using polymorphism mapping in Caenorhabditis elegans as our model for validation. We also report an alternative approach for mutation identification from traditional recombinant crosses, and a solution to the technical challenge of sequencing sterile or terminally arrested strains where population size is limiting. The methods described herein extend the applicability of whole-genome sequencing to a broader spectrum of mutations, including classes that are difficult to map by traditional means. Genetics Society of America 2016-03-04 /pmc/articles/PMC4856081/ /pubmed/26945029 http://dx.doi.org/10.1534/g3.116.028316 Text en Copyright © 2016 Smith et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Smith, Harold E.
Fabritius, Amy S.
Jaramillo-Lambert, Aimee
Golden, Andy
Mapping Challenging Mutations by Whole-Genome Sequencing
title Mapping Challenging Mutations by Whole-Genome Sequencing
title_full Mapping Challenging Mutations by Whole-Genome Sequencing
title_fullStr Mapping Challenging Mutations by Whole-Genome Sequencing
title_full_unstemmed Mapping Challenging Mutations by Whole-Genome Sequencing
title_short Mapping Challenging Mutations by Whole-Genome Sequencing
title_sort mapping challenging mutations by whole-genome sequencing
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4856081/
https://www.ncbi.nlm.nih.gov/pubmed/26945029
http://dx.doi.org/10.1534/g3.116.028316
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