A High-Density Single Nucleotide Polymorphism Map for Neurospora crassa

被引:46
|
作者
Lambreghts, Randy [1 ]
Shi, Mi [1 ]
Belden, William J. [1 ]
DeCaprio, David [3 ,4 ]
Park, Danny [3 ,4 ]
Henn, Matthew R. [3 ,4 ]
Galagan, James E. [3 ,4 ]
Bastuerkmen, Meray [5 ]
Birren, Bruce W. [3 ,4 ]
Sachs, Matthew S. [5 ]
Dunlap, Jay C. [1 ]
Loros, Jennifer J. [1 ,2 ]
机构
[1] Dartmouth Med Sch, Dept Genet, Hanover, NH 03755 USA
[2] Dartmouth Med Sch, Dept Biochem, Hanover, NH 03755 USA
[3] MIT, Broad Inst, Cambridge, MA 02142 USA
[4] Harvard Univ, Cambridge, MA 02142 USA
[5] Oregon Hlth & Sci Univ, Dept Environment & Biomol Syst, Beaverton, OR 97006 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-KINASE; MARKERS; GENES; IDENTIFICATION; RECOMBINATION; SEQUENCE; MUTATION; REGIONS; LOCI;
D O I
10.1534/genetics.108.089292
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:767 / 781
页数:15
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