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Updated: Aug 16, 2026

Spatiotemporal Analysis of Cytokinetic Events in Fission Yeast
Published on: February 20, 2017
Fission yeast MO25 protein is localized at SPB and septum and is essential for cell morphogenesis
Muneyoshi Kanai1, Kazunori Kume, Kohji Miyahara
1Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi Hiroshima, Japan.
Abstract:
Cell morphogenesis is of fundamental significance in all eukaryotes for development, differentiation, and cell proliferation. In fission yeast, Drosophila Furry-like Mor2 plays an essential role in cell morphogenesis in concert with the NDR/Tricornered kinase Orb6. Mutations of these genes result in the loss of cell polarity. Here we show that the conserved proteins, MO25-like Pmo25, GC kinase Nak1, Mor2, and Orb6, constitute a morphogenesis network that is important for polarity control and cell separation. Intriguingly, Pmo25 was localized at the mitotic spindle pole bodies (SPBs) and then underwent translocation to the dividing medial region upon cytokinesis. Pmo25 formed a complex with Nak1 and was required for both the localization and kinase activity of Nak1. Pmo25 and Nak1 in turn were essential for Orb6 kinase activity. Further, the Pmo25 localization at the SPBs and the Nak1-Orb6 kinase activities during interphase were under the control of the Cdc7 and Sid1 kinases in the septation initiation network (SIN), suggesting a functional linkage between SIN and the network for cell morphogenesis/separation following cytokinesis.
Insights
A novel network involving Pmo25, Nak1, Mor2, and Orb6 proteins controls cell morphogenesis and polarity in fission yeast. This pathway links the septation initiation network (SIN) to cell division and separation processes.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Cell morphogenesis is crucial for eukaryotic development, differentiation, and proliferation.
- Fission yeast Mor2 and Orb6 kinase are vital for cell polarity, with mutations causing polarity loss.
Purpose of the Study:
- To elucidate the roles of conserved proteins Pmo25, Nak1, Mor2, and Orb6 in cell morphogenesis and polarity control.
- To investigate the functional interactions within this protein network and its connection to other cellular pathways.
Main Methods:
- Protein localization studies using microscopy.
- Co-immunoprecipitation to assess protein complex formation.
- Kinase activity assays.
- Genetic analysis of mutant phenotypes.
Main Results:
- Pmo25, Nak1, Mor2, and Orb6 form a morphogenesis network essential for polarity and cell separation.
- Pmo25 localizes to spindle pole bodies and translocates during cytokinesis, forming a complex with Nak1.
- Pmo25 is required for Nak1 localization and activity, and both are essential for Orb6 kinase activity.
- The septation initiation network (SIN) kinases Cdc7 and Sid1 regulate Pmo25 localization and Nak1-Orb6 activity.
Conclusions:
- A conserved protein network (Pmo25, Nak1, Mor2, Orb6) is critical for fission yeast cell morphogenesis, polarity, and separation.
- This network exhibits a functional linkage with the septation initiation network (SIN), integrating cell division and morphogenesis pathways.
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