Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis

被引:37
作者
Brady, KP
Rowe, LB
Her, H
Stevens, TJ
Eppig, J
Sussman, DJ
Sikela, J
Beier, DR
机构
[1] HARVARD UNIV,SCH MED,BRIGHAM & WOMENS HOSP,DIV GENET,BOSTON,MA 02115
[2] JACKSON LAB,BAR HARBOR,ME 04605
[3] UNIV COLORADO,HLTH SCI CTR,DEPT PHARMACOL,DENVER,CO 80262
[4] UNIV MARYLAND,SCH MED,DIV HUMAN GENET,BALTIMORE,MD 21201
来源
GENOME RESEARCH | 1997年 / 7卷 / 11期
关键词
D O I
10.1101/gr.7.11.1085
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
We have demonstrated previously that noncoding sequences of genes are a robust source of polymorphisms between mouse species when tested using single-strand conformation polymorphism (SSCP) analysis, and that these polymorphisms are useful for genetic mapping. In this report we demonstrate that presumptive 3'-untranslated region sequence obtained from expressed sequence tags (ESTs) can be analyzed in a similar fashion, and we have used this approach to map 262 loci using an interspecific backcross. These results demonstrate SSCP analysis of genes or ESTs is a simple and efficient means for the genetic localization of transcribed sequences, and is furthermore an approach that is applicable to any system for which there is sufficient sequence polymorphism.
引用
收藏
页码:1085 / 1093
页数:9
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