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Table of strains used in this study [Dataset]

Year: 2025
Type: dataset
Abstract: Eukaryotic chromosome segregation relies on the assembly of a bipolar machinery based on microtubules (MTs), named the mitotic spindle. Formation of the mitotic spindle follows a force balance mechanism that ensures the proper capture and separation of sister chromatids. Many proteins have been involved in the establishment of this force balance, although kinesin 5 is well recognized as the major outward pushing force generator, since its inactivation results in monopolar, non-functional spindles. In order to find additional players in the force balance mechanism, we have performed a suppressor screen using a conditional allele of the fission yeast kinesin 5 ortholog Cut7. This screen identified that the lack of the PP6 phosphatase partially suppresses cut7 phenotypes, at least by defective translation of MT regulators, such as the minus end-directed kinesin Klp2, the MT stabilizer Alp7 and the MT bundler Ase1, impacting on the force balance mechanism. Additionally, our data show that the Elongator complex, a target activated by PP6 for efficient tRNA modification, also contributes to the force balance, albeit to a lesser extent. Importantly, this complex has recently been implicated in direct MT polymerization in metazoans, a role not shared by its fission yeast counterpart.
Authors: Marín, Laura, Castro-Sangrador, Jorge, Hoya, Marta, Tello, Shara, Coll, Pedro M., Encinar del Dedo, Javier, Fernández-Álvarez, Alfonso, Ribas, Juan Carlos, Tran, Phong T., Rincon, Sergio A.
Language: English
Subfield: Cell Biology
Open Access status: green
OpenAlex ID: W7111156739
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