Effects of the myosin inhibitor 2,3-butanedione monoxime on the physiologyof fission yeast

Citation
G. Steinberg et Jr. Mcintosh, Effects of the myosin inhibitor 2,3-butanedione monoxime on the physiologyof fission yeast, EUR J CELL, 77(4), 1998, pp. 284-293
Citations number
79
Categorie Soggetti
Cell & Developmental Biology
Journal title
EUROPEAN JOURNAL OF CELL BIOLOGY
ISSN journal
01719335 → ACNP
Volume
77
Issue
4
Year of publication
1998
Pages
284 - 293
Database
ISI
SICI code
0171-9335(199812)77:4<284:EOTMI2>2.0.ZU;2-6
Abstract
F-actin and associated myosins are thought to take part in a wide range of cellular processes, like motility and contraction, polarized growth, and se cretion. The reagent 2,3-butanedione monoxime (BDM) is a well characterized inhibitor of the contraction of vertebrate muscle that reversibly affects myosin function and influences the intracellular concentration of Ca2+. Her e we describe the influence of BDM on growth and division of the fission ye ast Schizosaccharomyces pombe. At concentrations from 1-30 mM, BDM graduall y inhibited formation and growth of S. pombe colonies on agar plates, with a lethal effect at greater than or equal to 15 mM. In strains of S. pombe t hat were blocked by elevated temperature from entry into mitosis, drug trea tment reversibly decreased microtubule-independent tip growth and septation , with an IC50 value around 12 mM; nuclear division, on the other hand, was essentially unaffected by up to 15 mM BDM, At 30 mM BDM the secretion of i nvertase, which required both F-actin and microtubules, was decreased to th e same extent as that seen when cytochalasin D was used to disrupt F-actin. However, the actin cytoskeleton was insensitive to up to 10 mM BDM, while the actin patches lost their polar distribution at 20-30 mM BDM, Cells trea ted with 5-20 mM BDM for 3 hours and then high pressure frozen did not show an accumulation of secretory vesicles. However, 10 mM BDM treatment disorg anized the fungal cell wad, resulting in some unusually thick parts lying n ext to regions were the wall was almost absent. These defects could be resc ued by incubating the cells in inhibitors of glucanases, Osmolytic stabiliz ation with sorbitol rescued the effect of 15 mM BDM on colony survival, ind icating that the secretion of wall components and/or wall-modifying enzymes may be the principal reason for cell death caused by BDM, Our results are consistent with the hypothesis that BDM influences actin-dependent processe s in fission yeast and that actomyosin-dependent motility contributes to th e secretory process of tip growth.