High-resolution, high-throughput SNP mapping in Drosophila melanogaster

被引:0
|
作者
Chen D. [1 ]
Ahlford A. [2 ]
Schnorrer F. [1 ]
Kalchhauser I. [1 ]
Fellner M. [1 ,3 ]
Viràgh E. [4 ]
Kiss I. [4 ]
Syvänen A.-C. [2 ]
Dickson B.J. [1 ]
机构
[1] Research Institute of Molecular Pathology (IMP), A-1030 Vienna
[2] Uppsala University, Department of Medical Sciences, Molecular Medicine, S-75185 Uppsala
[3] Institute of Molecular Biotechnology of the Austrian Academy of Sciences, A-1030 Vienna
[4] Biological Research Centre, Hungarian Academy of Sciences, H-6701 Szeged
基金
奥地利科学基金会;
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D O I
10.1038/nmeth.1191
中图分类号
学科分类号
摘要
Single nucleotide polymorphisms (SNPs) are useful markers for genetic mapping experiments in model organisms. Here we report the establishment of a high-density SNP map and high-throughput genotyping assays for Drosophila melanogaster. Our map comprises 27,367 SNPs in common laboratory Drosophila stocks. These SNPs were clustered within 2,238 amplifiable markers at an average density of 1 marker every 50.3 kb, or 6.3 genes. We have also constructed a set of 62 Drosophila stocks, each of which facilitates the generation of recombinants within a defined genetic interval of 1-2 Mb. For flexible, high-throughput SNP genotyping, we used fluorescent tag-array mini-sequencing (TAMS) assays. We designed and validated TAMS assays for 293 SNPs at an average resolution of 391.3 kb, and demonstrated the utility of these tools by rapidly mapping 14 mutations that disrupt embryonic muscle patterning. These resources enable high-resolution high-throughput genetic mapping in Drosophila.
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页码:323 / 329
页数:6
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