FISHing for chick genes:: Triple-label whole-mount fluorescence in situ hybridization detects simultaneous and overlapping gene expression in avian embryos

被引:53
作者
Denkers, N
García-Villalba, P
Rodesch, CK
Nielson, KR
Mauch, TJ
机构
[1] Univ Utah, Sch Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Sch Med, Fluorescence Microscopy Core, Salt Lake City, UT USA
关键词
fluorescence in situ hybridization; whole-mount; chick; avian; embryo; confocal; colocalization; mesoderm; pax-2; paraxis; chordin;
D O I
10.1002/dvdy.20005
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Multi-color whole-mount in situ hybridization is a powerful technique for comparing the spatial expression patterns of two or more genes in developing embryos. We have developed an amplified triple-label whole-mount fluorescence in situ hybridization (FISH) protocol that permits detection of three different mRNAs in a single embryo. Our protocol uses simultaneous in situ hybridization to haptenylated riboprobes, followed by sequential antibody detection using anti-hapten antibodies conjugated to horseradish peroxidase, and the tyramide signal amplification (TSA) fluorescence detection system. Conventional fluorescence microscopy identifies areas of overlapping gene expression at the tissue level, whereas confocal fluorescence microscopy permits single-cell resolution and differentiates specialized cell types within a given tissue. This protocol will provide researchers engaged in the use of FISH with a solid starting point for adapting their own in situ hybridization protocols, either alone or in combination with immunohistochemistry or green fluorescence protein colocalization. Developmental Dynamics 229.651-657, 2004. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:651 / 657
页数:7
相关论文
共 29 条