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Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over

BACKGROUND: Exome sequencing has become a popular method to evaluate undirected mutagenesis experiments in mice. However, the most suitable mouse strain for the biological model may be relatively distant from the standard mouse reference genome. For pinpointing causative variants, a matching referen...

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Autores principales: Derdak, Sophia, Sabrautzki, Sibylle, de Angelis, Martin Hrabě, Gut, Marta, Gut, Ivo G, Beltran, Sergi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422528/
https://www.ncbi.nlm.nih.gov/pubmed/25943197
http://dx.doi.org/10.1186/s12864-015-1548-7
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author Derdak, Sophia
Sabrautzki, Sibylle
de Angelis, Martin Hrabě
Gut, Marta
Gut, Ivo G
Beltran, Sergi
author_facet Derdak, Sophia
Sabrautzki, Sibylle
de Angelis, Martin Hrabě
Gut, Marta
Gut, Ivo G
Beltran, Sergi
author_sort Derdak, Sophia
collection PubMed
description BACKGROUND: Exome sequencing has become a popular method to evaluate undirected mutagenesis experiments in mice. However, the most suitable mouse strain for the biological model may be relatively distant from the standard mouse reference genome. For pinpointing causative variants, a matching reference with gene annotations is essential, but not always readily available. RESULTS: We present an approach that allows to use murine Ensembl annotations on alternative mouse strain assemblies. We resolved ENU-induced mutation screening for 8 phenotypic mutant lines generated on C3HeB/FeJ background aligning the sequences against the closely related, but not annotated reference of C3H/HeJ. Variants occurring in all strains were filtered out as specific for the C3HeB/FeJ strain but unrelated to mutagenesis. Variants occurring exclusively in all individuals of one mutant line and matching the inheritance model were selected as mutagenesis-related. These variants were annotated with gene and exon names lifted over from the standard murine reference mm9 to C3H/HeJ using megablast. For each mutant line, we could restrict the results to exonic variants in between 1 and 23 genes. CONCLUSIONS: The presented method of exonic annotation lift-over proved to be a valuable tool in the search for mutagenesis-derived coding genomic variants and the assessment of genotype-phenotype relationships.
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spelling pubmed-44225282015-05-07 Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over Derdak, Sophia Sabrautzki, Sibylle de Angelis, Martin Hrabě Gut, Marta Gut, Ivo G Beltran, Sergi BMC Genomics Methodology Article BACKGROUND: Exome sequencing has become a popular method to evaluate undirected mutagenesis experiments in mice. However, the most suitable mouse strain for the biological model may be relatively distant from the standard mouse reference genome. For pinpointing causative variants, a matching reference with gene annotations is essential, but not always readily available. RESULTS: We present an approach that allows to use murine Ensembl annotations on alternative mouse strain assemblies. We resolved ENU-induced mutation screening for 8 phenotypic mutant lines generated on C3HeB/FeJ background aligning the sequences against the closely related, but not annotated reference of C3H/HeJ. Variants occurring in all strains were filtered out as specific for the C3HeB/FeJ strain but unrelated to mutagenesis. Variants occurring exclusively in all individuals of one mutant line and matching the inheritance model were selected as mutagenesis-related. These variants were annotated with gene and exon names lifted over from the standard murine reference mm9 to C3H/HeJ using megablast. For each mutant line, we could restrict the results to exonic variants in between 1 and 23 genes. CONCLUSIONS: The presented method of exonic annotation lift-over proved to be a valuable tool in the search for mutagenesis-derived coding genomic variants and the assessment of genotype-phenotype relationships. BioMed Central 2015-05-06 /pmc/articles/PMC4422528/ /pubmed/25943197 http://dx.doi.org/10.1186/s12864-015-1548-7 Text en © Derdak et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Derdak, Sophia
Sabrautzki, Sibylle
de Angelis, Martin Hrabě
Gut, Marta
Gut, Ivo G
Beltran, Sergi
Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
title Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
title_full Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
title_fullStr Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
title_full_unstemmed Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
title_short Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
title_sort genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422528/
https://www.ncbi.nlm.nih.gov/pubmed/25943197
http://dx.doi.org/10.1186/s12864-015-1548-7
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