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FEBS J. 2014 Oct;281(20):4612-21. doi: 10.1111/febs.12965. Epub 2014 Sep 6.

3,6-Epidioxy-1,10-bisaboladiene inhibits G1 -specific transcription through Swi4/Swi6 and Mbp1/Swi6 via the Hog1 stress pathway in yeast.

Author information

1
Department of Molecular Biotechnology, Hiroshima University, Japan; Department of Biochemistry, University of Occupational and Environmental Health, Kitakyushu City, Japan.

Abstract

3,6-Epidioxy-1,10-bisaboladiene (EDBD), a bisabolane sesquiterpene endoperoxide compound, was previously isolated from Cacalia delphiniifolia and C. hastata in northern Japan. EDBD has cytotoxic effects and induces apoptosis via phosphorylation of p38 mitogen-activated protein kinase in human promyelocytic leukemia HL60 cells. However, the mechanism of action of EDBD has not yet been fully elucidated. In this study, we examined the molecular mechanisms of EDBD in the budding yeast Saccharomyces cerevisiae. EDBD arrested the growth of S. cerevisiae cells by suppressing progression from the G1 phase to the S phase and from the G2 phase to the M phase. Moreover, biochemical and genetic analyses revealed that EDBD activated environmental stress-response pathways involving Hog1 and affected Cln3/G1 cyclin activity, thereby inhibiting the expression of SCB-binding factor and MCB-binding factor target genes. Our results provided important insights into the functions of EDBD in tumor cells and may facilitate the development of EDBD-based antitumor therapies.

STRUCTURED DIGITAL ABSTRACT:

•Swi4 physically interacts with Swi6 by anti tag coimmunoprecipitation (View interaction).

KEYWORDS:

3,6-epidioxy-1,10-bisaboladiene; G1 cyclin; Hog1; MCB-binding factor; SCB-binding factor

PMID:
25112483
DOI:
10.1111/febs.12965
[Indexed for MEDLINE]
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