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Molecular and Cellular Biology, December 1999, p. 8016-8027, Vol. 19, No. 12
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Bni1p Regulates Microtubule-Dependent Nuclear Migration through
the Actin Cytoskeleton in Saccharomyces cerevisiae
Takeshi
Fujiwara,1
Kazuma
Tanaka,2
Eiji
Inoue,1
Mitsuhiro
Kikyo,1 and
Yoshimi
Takai1,*
Department of Molecular Biology and
Biochemistry, Osaka University Graduate School of Medicine/Faculty of
Medicine, Suita, Osaka 565-0871,1 and
Division of Biochemistry, Cancer Institute, Hokkaido
University School of Medicine, Sapporo, Hokkaido
060-8638,2 Japan
Received 19 April 1999/Returned for modification 18 June
1999/Accepted 27 August 1999
The RHO1 gene encodes a yeast homolog of the mammalian
RhoA protein. Rho1p is localized to the growth sites and is required for bud formation. We have recently shown that Bni1p is one of the
potential downstream target molecules of Rho1p. The BNI1
gene is implicated in cytokinesis and the establishment of cell
polarity in Saccharomyces cerevisiae but is not essential
for cell viability. In this study, we screened for mutations that were
synthetically lethal in combination with a bni1 mutation
and isolated two genes. They were the previously identified
PAC1 and NIP100 genes, both of which are
implicated in nuclear migration in S. cerevisiae. Pac1p is
a homolog of human LIS1, which is required for brain development,
whereas Nip100p is a homolog of rat p150Glued, a component
of the dynein-activated dynactin complex. Disruption of
BNI1 in either the pac1 or nip100
mutant resulted in an enhanced defect in nuclear migration, leading to
the formation of binucleate mother cells. The arp1 bni1
mutant showed a synthetic lethal phenotype while the cin8
bni1 mutant did not, suggesting that Bni1p functions in a kinesin
pathway but not in the dynein pathway. Cells of the pac1
bni1 and nip100 bni1 mutants exhibited a random
distribution of cortical actin patches. Cells of the pac1
act1-4 mutant showed temperature-sensitive growth and a nuclear
migration defect. These results indicate that Bni1p regulates
microtubule-dependent nuclear migration through the actin cytoskeleton.
Bni1p lacking the Rho-binding region did not suppress the pac1
bni1 growth defect, suggesting a requirement for the Rho1p-Bni1p
interaction in microtubule function.
*
Corresponding author. Mailing address: Department of
Molecular Biology and Biochemistry, Osaka University Graduate School of
Medicine/Faculty of Medicine, Suita, Osaka 565-0871, Japan. Phone:
81-6-6879-3410. Fax: 81-6-6879-3419. E-mail:
ytakai{at}molbio.med.osaka-u.ac.jp.
Molecular and Cellular Biology, December 1999, p. 8016-8027, Vol. 19, No. 12
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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