Affiliation:
1. Institute of Molecular and Cell Biology, National University of Singapore, Singapore 117609, Singapore, 1 and
2. School of Biological Sciences, University of Manchester, Manchester M13 9PT, United Kingdom2
Abstract
ABSTRACT
cdc28-1N
mutants progress through the G
1
and S phases normally at the restrictive temperature but fail to undergo nuclear division. We have isolated a gene,
NDD1
, which at a high dosage suppresses the nuclear-division defect of
cdc28-1N. NDD1
(nuclear division defective) is an essential gene. Its expression during the cell cycle is tightly regulated such that
NDD1
RNA is most abundant during the S phase. Cells lacking the
NDD1
gene arrest with an elongated bud, a short mitotic spindle, 2N DNA content, and an undivided nucleus, suggesting that its function is required for some aspect of nuclear division. We show that overexpression of Ndd1 results in the upregulation of both
CLB1
and
CLB2
transcription, suggesting that the suppression of
cdc28-1N
by
NDD1
may be due to an accumulation of these cyclins. Overproduction of Ndd1 also enhances the expression of
SWI5
, whose transcription, like that of
CLB1
and
CLB2
, is activated in the late S phase. Ndd1 is essential for the expression of
CLB1
,
CLB2
, and
SWI5
, since none of these genes are transcribed in its absence. Both
CLB2
expression and its upregulation by
NDD1
are mediated by a 240-bp promoter sequence that contains four
MCM1
-binding sites. However, Ndd1 does not appear to be a component of any of the protein complexes assembled on this DNA fragment, as indicated by gel mobility shift assays. Instead, overexpression of
NDD1
prevents the formation of one of the complexes whose appearance correlates with the termination of
CLB2
expression in G
1
. The inability of
GAL1
promoter-driven
CLB2
to suppress the lethality of
NDD1
null mutant suggests that, in addition to
CLB1
and
CLB2
,
NDD1
may also be required for the transcription of other genes whose functions are necessary for G
2
/M transition.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
62 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献