Identification of mutants with increased variation in cell size at onset of mitosis in fission yeast

Author:

Scotchman Elizabeth1ORCID,Kume Kazunori123,Navarro Francisco J.1ORCID,Nurse Paul14ORCID

Affiliation:

1. Cell Cycle Laboratory, The Francis Crick Institute, London NW1 1AT, UK

2. Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8530, Japan

3. Hiroshima Research Center for Healthy Aging (HiHA), Hiroshima University,Higashi-Hiroshima, Hiroshima 739-8530, Japan

4. Laboratory of Yeast Genetics and Cell Biology, Rockefeller University, New York, NY 10065, USA

Abstract

ABSTRACT Fission yeast cells divide at a similar cell length with little variation about the mean. This is thought to be the result of a control mechanism that senses size and corrects for any deviations by advancing or delaying onset of mitosis. Gene deletions that advance cells into mitosis at a smaller size or delay cells entering mitosis have led to the identification of genes potentially involved in this mechanism. However, the molecular basis of this control is still not understood. In this work, we have screened for genes that when deleted increase the variability in size of dividing cells. The strongest candidate identified in this screen was mga2. The mga2 deletion strain shows a greater variation in cell length at division, with a coefficient of variation (CV) of 15–24%, while the wild-type strain has a CV of 5–8%. Furthermore, unlike wild-type cells, the mga2 deletion cells are unable to correct cell size deviations within one cell cycle. We show that the mga2 gene genetically interacts with nem1 and influences the nuclear membrane and the nuclear–cytoplasmic transport of CDK regulators.

Funder

Cancer Research UK

Medical Research Council

Wellcome Trust

Breast Cancer Research Foundation

Japan Society for the Promotion of Science

Publisher

The Company of Biologists

Subject

Cell Biology

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