Volume 272, Number 41,
Issue of October 10, 1997
pp. 25768-25777
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Mts4, a Non-ATPase Subunit of the 26 S Protease in Fission Yeast
Is Essential for Mitosis and Interacts Directly with the ATPase Subunit
Mts2
(Received for publication, January 30, 1997, and in revised form, June 23, 1997)
Caroline R. M.
Wilkinson
,
Mairi
Wallace
,
Michael
Seeger
¶
,
Wolfgang
Dubiel
¶
and
Colin
Gordon
From the
MRC Human Genetics Unit, Western General
Hospital, Crewe Road, Edinburgh, EH4 2XU Scotland, United
Kingdom and the ¶ Institute of Biochemistry, Medical Faculty,
Humboldt University, Monbijoustrasse 2A 10117, Berlin, Federal
Republic of Germany
We have isolated a fission yeast gene,
mts4+, by complementation of a
temperature-sensitive mutation and show that it encodes subunit 2 (S2)
of the 19 S regulatory complex of the 26 S protease. mts4+ is an essential gene, and we show that
loss of this subunit causes cells to arrest in metaphase, illustrating
the importance of S2 for mitosis. The Mts4 protein is 48% identical to
S2 of the human 26 S protease, and the lethal phenotype of the null
mts4 allele can be rescued by the human cDNA encoding
S2. We provide genetic and physical evidence to suggest that the Mts4
protein interacts with the product of the mts2+
gene, an ATPase which has previously been shown to be subunit 4 of the
26 S protease.