Genetic linkage mapping of zebrafish genes and ESTs

被引:76
作者
Kelly, PD
Chu, F
Woods, IG
Ngo-Hazelett, P
Cardozo, T
Huang, H
Kimm, F
Liao, LY
Yan, YL
Zhou, YY
Johnson, SL
Abagyan, R
Schier, AF
Postlethwait, JH
Talbot, WS [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[2] Univ Oregon, Inst Neurosci, Eugene, OR 97405 USA
[3] NYU, Sch Med, Skirball Inst Biomol Med, New York, NY 10016 USA
关键词
D O I
10.1101/gr.10.4.558
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Generic screens in zebrafish (Danio rerio) have isolated mutations in hundreds of genes essential for vertebrate development, physiology, and behavior. We have constructed a genetic linkage map that will facilitate the identification of candidate genes for these mutations and allow comparisons among the genomes of zebrafish and other vertebrates. On this map, we have localized 771 zebrafish genes and expressed sequence tags (ESTs) by scoring single-stranded conformational polymorphisms (SSCPs) in a meiotic mapping panel. Of these sequences, 642 represent previously unmapped genes and ESTs. The mapping panel was comprised of 42 homozygous diploid individuals produced by hear shock treatment of haploid embryos at the one-cell stage (HS diploids). This "doubled haploid" strategy combines the advantages of mapping in haploid and standard diploid systems, because heat shock diploid individuals have only one allele at each locus and can survive to adulthood, enabling a relatively large quantity of genomic DNA to be prepared from each individual in the mapping panel. To integrate this map with others, we also scored 593 previously mapped simple-sequence length polymorphisms (SSLPs) in the mapping panel. This map will accelerate the molecular analysis of zebrafish mutations and facilitate comparative analysis of vertebrate genomes.
引用
收藏
页码:558 / 567
页数:10
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