PUBLICATION
Effect of inhibitors of DNA replication on early zebrafish embryos: evidence for coordinate activation of multiple intrinsic cell-cycle checkpoints at the mid-blastula transition
- Authors
- Ikegami, R., Rivera-Bennetts, A.K., Brooker, D.L., and Yager, T.D.
- ID
- ZDB-PUB-971203-12
- Date
- 1997
- Source
- Zygote (Cambridge, England) 5(2): 153-175 (Journal)
- Registered Authors
- Ikegami, Richard, Yager, Tom
- Keywords
- none
- MeSH Terms
-
- Animals
- Aphidicolin/pharmacology
- Blastocyst/drug effects*
- Blastocyst/physiology*
- Camptothecin/pharmacology
- Cell Cycle/drug effects*
- DNA Replication/drug effects*
- Embryo, Nonmammalian/drug effects*
- Etoposide/pharmacology
- Gene Deletion
- Mutagenesis
- Time Factors
- Zebrafish
- PubMed
- 9276512 Full text @ Zygote
Citation
Ikegami, R., Rivera-Bennetts, A.K., Brooker, D.L., and Yager, T.D. (1997) Effect of inhibitors of DNA replication on early zebrafish embryos: evidence for coordinate activation of multiple intrinsic cell-cycle checkpoints at the mid-blastula transition. Zygote (Cambridge, England). 5(2):153-175.
Abstract
We address the developmental activation, in the zebrafish embryo, of intrinsic cell-cycle checkpoints which monitor the DNA replication process and progression through the cell cycle. Eukaryotic DNA replication is probably carried out by a multiprotein complex containing numerous enzymes and accessory factors that act in concert to effect processive DNA synthesis (Applegren, N. et al. (1995) J. Cell. Biochem. 59, 91-107). We have exposed early zebrafish embryos to three chemical agents which are predicted to specifically inhibit the DNA polymerase alpha, topoisomerase I and topoisomerase II components of the DNA replication complex. We present four findings: (1) Before mid-blastula transition (MBT) an inhibition of DNA synthesis does not block cells from attempting to proceed through mitosis, implying the lack of functional checkpoints. (2) After MBT, the embryo displays two distinct modes of intrinsic checkpoint operation. One mode is a rapid and complete stop of cell division, and the other is an 'adaptive' response in which the cell cycle continues to operate, perhaps in a 'repair' mode, to generate daughter nuclei with few visible defects. (3) The embryo does not display a maximal capability for the 'adaptive' response until several hours after MBT, which is consistent with a slow transcriptional control mechanism for checkpoint activation. (4) The slow activation of checkpoints at MBT provides a window of time during which inhibitors of DNA synthesis will induce cytogenetic lesions without killing the embryo. This could be useful in the design of a deletion-mutagenesis strategy.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping