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Updated: Aug 7, 2026

Examination of Mitotic and Meiotic Fission Yeast Nuclear Dynamics by Fluorescence Live-cell Microscopy
Published on: June 24, 2019
Fta2, an essential fission yeast kinetochore component, interacts closely with the conserved Mal2 protein
Anne Kerres1, Visnja Jakopec, Christoph Beuter
1Lehrstuhl für funktionelle Genomforschung der Mikroorganismen, Heinrich-Heine Universität, 40225 Düsseldorf, Germany.
Abstract:
The fission yeast multiprotein-component Sim4 complex plays a fundamental role in the assembly of a functional kinetochore. It affects centromere association of the histone H3 variant CENP-A as well as kinetochore association of the DASH complex. Here, multicopy suppressor analysis of a mutant version of the Sim4 complex component Mal2 identified the essential Fta2 kinetochore protein, which is required for bipolar chromosome attachment. Kinetochore localization of Mal2 and Fta2 depends on each other, and overexpression of one protein can rescue the phenotype of the mutant version of the other protein. fta2 mal2 double mutants were inviable, implying that the two proteins have an overlapping function. This close interaction with Fta2 is not shared by other Sim4 complex components, indicating the existence of functional subgroups within this complex. The Sim4 complex seems to be assembled in a hierarchical way, because Fta2 is localized correctly in a sim4 mutant. However, Fta2 kinetochore localization is reduced in a spc7 mutant. Spc7, a suppressor of the EB1 family member Mal3, is part of the conserved Ndc80-MIND-Spc7 kinetochore complex.
Insights
The Sim4 complex in fission yeast is crucial for kinetochore assembly. Researchers identified Fta2 as a key protein interacting with Mal2, essential for chromosome attachment and Sim4 complex function.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- The Sim4 complex is vital for kinetochore assembly in fission yeast.
- It influences CENP-A and DASH complex localization at the kinetochore.
Purpose of the Study:
- To identify novel proteins interacting with Sim4 complex components.
- To elucidate the functional roles of Mal2 and Fta2 in kinetochore function.
Main Methods:
- Multicopy suppressor analysis was used to identify Fta2.
- Genetic interactions and protein localization studies were performed.
Main Results:
- Fta2 was identified as an essential kinetochore protein required for bipolar chromosome attachment.
- Mal2 and Fta2 exhibit interdependent kinetochore localization and overlapping functions.
- Fta2 localization is dependent on the Sim4 complex but sensitive to Spc7 levels.
Conclusions:
- Fta2 and Mal2 form a functional subgroup within the Sim4 complex.
- The Sim4 complex assembly appears hierarchical, with Fta2's localization preceding its dependence on Spc7.
- These findings reveal functional specialization within the Sim4 complex and its hierarchical assembly.
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