Gene mapping in zebrafish using single-strand conformation polymorphism analysis

被引:19
|
作者
Förnzler, D
Her, H
Knapik, EW
Clark, M
Lehrach, H
Postlethwait, JH
Zon, LI
Beier, DR
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA 02114 USA
[3] Max Planck Inst Mol Genet, Berlin, Germany
[4] Univ Oregon, Inst Neurosci, Eugene, OR 97403 USA
[5] Harvard Univ, Childrens Hosp, Sch Med, HHMI, Boston, MA 02115 USA
[6] Harvard Univ, Childrens Hosp, Sch Med, Div Hematol Oncol, Boston, MA 02115 USA
关键词
D O I
10.1006/geno.1998.5386
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To exploit fully the power of the zebrafish system as a model for vertebrate development, it will be necessary to develop efficient tools for genomic analysis. In this report we have tested whether single-strand conformation polymorphism analysis (SSCP) can be utilized for gene mapping in zebrafish. Over 100 primer pairs derived from noncoding regions of known genes and partially characterized cDNAs were analyzed, and a polymorphism frequency of approximately 50% was detected in zebrafish strains used for genetic mapping studies. A subset of these polymorphic cDNAs was localized on the zebrafish map. SSCP thus represents an efficient strategy for mapping transcribed sequences with a high resolution in the zebrafish genome, which will facilitate the integration of existing zebrafish framework maps, the generation of a zebrafish EST map, and the application of alternative gene localization strategies such as comparative mapping. (C) 1998 Academic Press.
引用
收藏
页码:216 / 222
页数:7
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