D. Knapp et al., THE TRANSCRIPTION FACTOR SWI5 REGULATES EXPRESSION OF THE CYCLIN KINASE INHIBITOR P40(SIC1), Molecular and cellular biology, 16(10), 1996, pp. 5701-5707
DNA replication in budding yeast cells depends on the activation of th
e Cdc28 kinase (Gdk1 of Saccharomyces cerevisiae) associated with B-ty
pe cyclins Glb1 to Clb6, Activation of the kinase depends on proteolys
is of the Cdk inhibitor p40(SIC1) in late G(1), which is mediated by t
he ubiquitin-conjugating enzyme Cdc34 and two other proteins, Cdc4 and
Cdc53. Inactivation of any one of these three proteins prevents p40(S
IC1) degradation and causes cells to arrest in G(1) with active Cln ki
nases but no Clb-associated Cdc28 kinase activity, Deletion of SIC1 al
lows these mutants to replicate. p40(SIC1) disappears at the G(1)/S tr
ansition and reappears only after nuclear division, Cell cycle-regulat
ed proteolysis seems largely responsible for this pattern, but transcr
iptional control could also contribute; SIC1 RNA accumulates to high l
evels as cells exit M phase, To identify additional factors necessary
for the inhibition of the Cdk1/Cdc28 kinase in G(1), we isolated mutan
ts that can replicate DNA in the absence of Cdc4 function, Mutations i
n three loci (SIC1, SW15, and RIC3) were identified, We have shown tha
t high SIC1 transcript levels at late M phase depend on Swi5. Swi5 acc
umulates in the cytoplasm during S, G(2), and M phases of the cell cyc
le but enters the nuclei at late anaphase, Our data suggest that cell
cycle-regulated nuclear accumulation of Swi5 is responsible for the bu
rst of SIC1 transcription at the end of anaphase. This transcriptional
control may be important for inactivation of the Clb/Cdk1 kinase in G
(2)/M transition and during the subsequent G(1) period.