High Resolution Whole Mount In Situ Hybridization within Zebrafish Embryos to Study Gene Expression and Function
- Authors
- Chitramuthu, B.P., and Bennett, H.P.
- ID
- ZDB-PUB-131203-28
- Date
- 2013
- Source
- Journal of visualized experiments : JoVE (80): e50644 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Embryo Culture Techniques/methods*
- Embryo, Nonmammalian
- Humans
- In Situ Hybridization/methods*
- RNA Probes/chemistry
- RNA Probes/genetics
- RNA, Antisense/chemistry
- RNA, Antisense/genetics
- Zebrafish/embryology*
- Zebrafish/genetics*
- PubMed
- 24192694 Full text @ J. Vis. Exp.
This article focuses on whole-mount in situ hybridization (WISH) of zebrafish embryos. The WISH technology facilitates the assessment of gene expression both in terms of tissue distribution and developmental stage. Protocols are described for the use of WISH of zebrafish embryos using antisense RNA probes labeled with digoxigenin. Probes are generated by incorporating digoxigenin-linked nucleotides through in vitro transcription of gene templates that have been cloned and linearized. The chorions of embryos harvested at defined developmental stages are removed before incubation with specific probes. Following a washing procedure to remove excess probe, embryos are incubated with anti-digoxigenin antibody conjugated with alkaline phosphatase. By employing a chromogenic substrate for alkaline phosphatase, specific gene expression can be assessed. Depending on the level of gene expression the entire procedure can be completed within 2-3 days.