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Updated: Aug 11, 2026

Gibberella zeae Ascospore Production and Collection for Microarray Experiments.
Published on: November 30, 2006
Abstract:
The mitotic nuclear (equivalent to cell) cycle of the oomycete fungus, Saprolegnia ferax, was analysed by quantitative serial-section electron microscopy of hyphal nuclear populations synchronized by inhibition of DNA synthesis by fluorodeoxyuridine (FdUrd). Following telophase and karyokinesis, kinetochore mitrotubules persist into G1 stage as a single group of approximately 42 per nucleus (2n = 42 for this species). During G1 the centrioles replicate and kinetochore microtubules separate into 2 groups of approximately 21, a configuration they retain through S and G2. During metaphase a new population of kinetochore microtubules are formed, each one of an amphitelic pair connecting to the opposite pole to that associated with the persistent microtubule from the previous division. Thus, by the end of metaphase, there are approximately 42 kinetochore microtubules per half spindle. FdUrd, applied for 2 h with uracil, completely blocks DNA synthesis yet permits centriole replication and causes nuclei to accumulate with 2 pairs of centrioles, 2 arrays (each of 21) of kinetochore microtubules, and apparently enlarged nucleoli. Removal of FdUrd permits rapid (within 30 min) DNA synthesis followed by successive rounds of decreasingly synchronous nuclear cycles. These post-FdUrd cycles are 2.5 times longer than normal at 2.5 h, with S plus G2 being more extended than other phases. Calculated durations of a normal nuclear cycle are: G1, 33 min; S, 7 min; G2, 10 min; metaphase, 8 min; anaphase, 0.5 min; and telophase, 4 min.
Insights
The study reveals that kinetochore microtubules persist into G1 in Saprolegnia ferax. Fluorodeoxyuridine (FdUrd) synchronization highlights centriole replication and microtubule dynamics during the oomycete nuclear cycle.
Area of Science:
- Cell Biology
- Mycology
- Oomycete Research
Background:
- The nuclear cell cycle in oomycetes, like Saprolegnia ferax, is crucial for fungal growth and development.
- Understanding the dynamics of nuclear division, including microtubule organization, is key to oomycete biology.
Purpose of the Study:
- To analyze the mitotic nuclear cell cycle of the oomycete fungus Saprolegnia ferax.
- To investigate the behavior of kinetochore microtubules and centrioles during nuclear division.
Main Methods:
- Quantitative serial-section electron microscopy was employed.
- Nuclear populations were synchronized using fluorodeoxyuridine (FdUrd) to inhibit DNA synthesis.
Main Results:
- Kinetochore microtubules persist into G1, organizing into distinct arrays.
- Centriole replication occurs during G1, with microtubules separating into two groups.
- FdUrd treatment blocks DNA synthesis, leading to nuclear accumulation with specific microtubule and centriole configurations.
- Removal of FdUrd initiates DNA synthesis and subsequent nuclear cycles, with extended S and G2 phases.
Conclusions:
- The study elucidates the precise behavior of kinetochore microtubules and centrioles throughout the Saprolegnia ferax nuclear cycle.
- FdUrd serves as an effective tool for synchronizing oomycete nuclear division, facilitating detailed cell cycle analysis.
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