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PMID: 21196518 Published · ppublish English Evaluation Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.

Genetics ·Vol. 187 ·No. 3 ·2011-03-00 ·Pages 633-41

Arnold CN, Xia Y, Lin P, Ross C, Schwander M, Smart NG, Müller U, Beutler B

Abstract

In a pedigree of C57BL/6J mice homozygous for germline mutations induced by the mutagen N-ethyl-N-nitrosourea (ENU), numerous animals died under specific pathogen-free (SPF) conditions between 6 and 7 months of age. Death was caused by nephritic syndrome, which progressed to renal failure associated with focal segmental glomerulosclerosis. To identify the mutation responsible for renal disease, we sequenced genomic DNA from an affected animal using the Applied Biosystems SOLiD sequencing platform. Approximately 74% of the nucleotides comprising coding sequences and splice junctions in the mouse genome were covered at least three times. Within this portion of the genome, 64 discrepancies were flagged as potential homozygous mutations and 82 were flagged as potential heterozygous mutations. A total of 10 of these calls, all homozygous, were validated by capillary sequencing. One of the validated mutations disrupted splicing of the Col4a4 transcript. Genetic mapping by bulk segregation analysis excluded all mutations but this one as the cause of renal disease in Aoba mice. Col4a4 has not been targeted in the mouse, and this strain, named Aoba, represents the first functionally null allele in this species. Our study demonstrates the speed and utility of whole genome sequencing coupled with low resolution meiotic mapping as a means of identifying causative mutations induced by ENU.

MeSH Terms
Alleles Animals Chromosome Mapping Chromosome Segregation Collagen Type IV/genetics DNA Mutational Analysis/methods Ethylnitrosourea/toxicity Genome Genome-Wide Association Study/methods Germ-Line Mutation/genetics Glomerulosclerosis, Focal Segmental/genetics Heterozygote Homozygote Mice Mice, Inbred C57BL Proteinuria/chemically induced,genetics RNA Splice Sites Renal Insufficiency/chemically induced,genetics
Chemicals
Collagen Type IV RNA Splice Sites Ethylnitrosourea
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Arnold Carrie N
Department of Genetics, Institute for Childhood and Neglected Disease, The Scripps Research Institute, La Jolla, California 92037, USA.
Xia Yu
Lin Pei
Ross Charles
Schwander Martin
Smart Nora G
Müller Ulrich
Beutler Bruce
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Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
1943-2631
Published
2011-03-00
Epub
2010-00-31
Pages
633-41
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC3063661
Subset
IM
Grants
NIAID NIH HHS · HHSN272200700038C · United States
NIDCD NIH HHS · R01 DC007704 · United States
NIDCD NIH HHS · DC005969 · United States
NIDCD NIH HHS · DC007704 · United States
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