A High-Density Single Nucleotide Polymorphism Map for Neurospora crassa

Author:

Lambreghts Randy1,Shi Mi1,Belden William J1,deCaprio David2,Park Danny2,Henn Matthew R2,Galagan James E2,Baştürkmen Meray3,Birren Bruce W2,Sachs Matthew S3,Dunlap Jay C1,Loros Jennifer J14

Affiliation:

1. Department of Genetics and

2. Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts 02142 and

3. Department of Environmental and Biomolecular Systems, Oregon Health & Science University, Beaverton, Oregon 97006

4. Department of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755

Abstract

Abstract We report the discovery and validation of a set of single nucleotide polymorphisms (SNPs) between the reference Neurospora crassa strain Oak Ridge and the Mauriceville strain (FGSC 2555), of sufficient density to allow fine mapping of most loci. Sequencing of Mauriceville cDNAs and alignment to the completed genomic sequence of the Oak Ridge strain identified 19,087 putative SNPs. Of these, a subset was validated by cleaved amplified polymorphic sequence (CAPS), a simple and robust PCR-based assay that reliably distinguishes between SNP alleles. Experimental confirmation resulted in the development of 250 CAPS markers distributed evenly over the genome. To demonstrate the applicability of this map, we used bulked segregant analysis followed by interval mapping to locate the csp-1 mutation to a narrow region on LGI. Subsequently, we refined mapping resolution to 74 kbp by developing additional markers, resequenced the candidate gene, NCU02713.3, in the mutant background, and phenocopied the mutation by gene replacement in the WT strain. Together, these techniques demonstrate a generally applicable and straightforward approach for the isolation of novel genes from existing mutants. Data on both putative and validated SNPs are deposited in a customized public database at the Broad Institute, which encourages augmentation by community users.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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