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Reference - PMID:34864879 - Complementation of fission yeast kinesin-5/Cut7 with human Eg5 provides a versatile platform for screening of anticancer compounds.

Reference summary

PubMed ID
PMID:34864879
Title
Complementation of fission yeast kinesin-5/Cut7 with human Eg5 provides a versatile platform for screening of anticancer compounds.
Authors
Hwang W, Toda T, Yukawa M
Citation
Biosci Biotechnol Biochem 2022 Jan 24;86(2):254-259
Publication year
2022
Abstract
Kinesin-5 family proteins are essential for bipolar spindle assembly to ensure mitotic fidelity. Here, we demonstrate evolutionary functional conservation of kinesin-5 between human and fission yeast. Human Eg5 expressed in the nucleus replaces fission yeast counterpart Cut7. Intriguingly, Eg5 overproduction results in cytotoxicity. This phenotype provides a useful platform for the development of novel kinesin-5 inhibitors as anticancer drugs.

Annotation

Complementation

PBO:0116194 - functionally complemented by human EG5

Genes:

Single locus phenotype

FYPO:0002061 - inviable vegetative cell population

Genes:

Genotypes:

FYPO:0003787 - long mitotic spindle microtubules protruding beyond spindle pole body

Genes:

Genotypes:

FYPO:0000276 - monopolar mitotic spindle

Genes:

Genotypes: