ZFIN ID: ZDB-PUB-070513-24
Identification of zygotic genes expressed at the midblastula transition in zebrafish
O'Boyle, S., Bree, R.T., McLoughlin, S., Grealy, M., and Byrnes, L.
Date: 2007
Source: Biochemical and Biophysical Research Communications   358(2): 462-468 (Journal)
Registered Authors: Bree, Ronan, Byrnes, Lucy, McLoughlin, Sarah, O'Boyle, Shaun
Keywords: Gene expression, Midblastula transition, Suppression subtractive hybridisation, Zebrafish
MeSH Terms:
  • Animals
  • Cell Cycle/physiology*
  • Cell Cycle Proteins/metabolism*
  • Cells, Cultured
  • Gene Expression Regulation, Developmental/physiology*
  • Zebrafish/embryology*
  • Zebrafish/metabolism*
  • Zygote/cytology*
  • Zygote/metabolism*
PubMed: 17490614 Full text @ Biochem. Biophys. Res. Commun.
Early development of the embryo is directed by maternal gene products and characterised by limited zygotic gene activity, cell division synchrony and no cell motility in several vertebrates including fish and frogs. At the midblastula transition (MBT), zygotic transcription is grossly activated, cells become motile and cell divisions become asynchronous. The aim of this study was to identify genes whose expression is up-regulated at the MBT in zebrafish. Suppression subtractive hybridisation (SSH) was employed to isolate 48 unique cDNAs, 28 of which show significant similarity to known genes and 20 represent novel cDNAs. Twenty one of these genes, with potential roles in transcriptional regulation, cell cycle control, and embryonic patterning showed increased expression at the MBT. Our results demonstrate the value of SSH as a tool to clone novel, zygotic, developmentally regulated genes that may be important in the progression of the MBT and embryonic patterning.