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Updated: Feb 10, 2026

Examination of Mitotic and Meiotic Fission Yeast Nuclear Dynamics by Fluorescence Live-cell Microscopy
Published on: June 24, 2019
The fission yeast SPB component Dms1 is required to initiate forespore membrane formation and maintain meiotic SPB
1Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka, Japan.
Abstract:
The spindle pole body (SPB) plays a central role in spore plasma membrane formation in addition to its recognized role in microtubule organization. During meiosis, a biomembrane called the forespore membrane (FSM) is newly formed at the SPB. Although several SPB proteins essential for the initiation of FSM formation (meiotic SPB components) have been identified, the molecular mechanism is still unknown. Here, we report the isolation and functional characterization of Dms1 as a component of the SPB. We show that FSM formation does not initiate in dms1Δ cells. Dms1 protein is constitutively expressed throughout the life cycle and localizes to the SPB and the nuclear envelope. The predicted Dms1 protein has a transmembrane domain, which is required for correct localization at the SPB. Dms1 is essential for the proper localization of three meiotic SPB components, Spo15, Spo2, and Spo13, but these components do not affect localization of Dms1. Collectively, these results suggest that Dms1 anchors these meiotic SPB components to the SPB, thereby facilitating the initiation of FSM formation.
Insights
The spindle pole body (SPB) is crucial for spore membrane formation. Dms1 protein anchors key SPB components, initiating forespore membrane formation during meiosis.
Area of Science:
- Cell Biology
- Molecular Biology
- Microbiology
Background:
- The spindle pole body (SPB) organizes microtubules and is vital for spore plasma membrane formation.
- The initiation of forespore membrane (FSM) formation at the SPB during meiosis involves several identified SPB proteins, but the precise molecular mechanism remains unclear.
Purpose of the Study:
- To isolate and functionally characterize Dms1 as a novel SPB component.
- To elucidate the role of Dms1 in the initiation of FSM formation during meiosis.
Main Methods:
- Isolation and functional characterization of the Dms1 protein.
- Analysis of Dms1 localization via its transmembrane domain.
- Investigating the localization of meiotic SPB components (Spo15, Spo2, Spo13) in dms1Δ cells.
Main Results:
- FSM formation is abolished in dms1Δ cells, indicating Dms1's essential role.
- Dms1 localizes to the SPB and nuclear envelope, requiring its transmembrane domain for SPB localization.
- Dms1 is necessary for the correct localization of Spo15, Spo2, and Spo13, but not vice versa.
Conclusions:
- Dms1 acts as an anchor for meiotic SPB components at the SPB.
- This anchoring function of Dms1 is critical for initiating forespore membrane formation during meiosis.
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