

Type of Document Master's Thesis Author Auckland, Ian Author's Email Address iaucklan@vt.edu URN etd-08242005-123051 Title Quantitative Analysis of a Cell Cycle Checkpoint in Xenopus laevis Cell-Free Egg Extracts Degree Master of Science Department Biology Advisory Committee
Advisor Name Title Sible, Jill C. Committee Chair Tyson, John J. Committee Member Walker, Richard A. Committee Member Keywords
- cell cycle
- Xenopus laevis
- nucleocytoplasmic ratio
- cyclin-dependent kinases (Cdk)
Date of Defense 2005-08-10 Availability unrestricted Abstract In somatic cells, checkpoint pathways trigger cell cycle arrest in response tounreplicated or damaged DNA by inhibiting the activity of cyclin-dependent kinases
(Cdks). In the Xenopus laevis embryo, checkpoints are not operational until the
midblastula transition (MBT). Studies in cell-free egg extracts indicate that a threshold
concentration of nuclei, which approximates the MBT concentration, is required to elicit
a checkpoint. The checkpoint response to unreplicated DNA in the extract prevents
transition into mitosis by inhibiting Cdk1/cyclin B, causing an increase in the minimum
amount of cyclin B necessary to enter mitosis, termed the cyclin threshold. Once the
threshold of cyclin is maintained or exceeded, the system will proceed into mitosis after a
lag time. We have investigated the relationship between nuclear concentration and cell
cycle regulation in the extract. By precisely regulating the concentration of cyclin B and
nuclear content in extract samples, we have found 1) the concentration of nuclei affects
cyclin B thresholds and lag time of entry into mitosis, 2) elevated cyclin thresholds
caused by DNA replication blocks are further increased by increasing the concentration
of nuclei, and 3) double-stranded DNA breaks in the extract system do not affect cyclin
thresholds or lag time of entry into mitosis within the range of nuclear concentrations that
can be efficiently replicated. This data provides evidence of the importance of the
nucleocytoplasmic ratio in normal cell cycle progression and its importance for
checkpoint acquisition during early Xenopus laevis development.
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