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Mol Cell Biol, May 1998, p. 2923-2931, Vol. 18, No. 5
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Molecular Evolution Allows Bypass of the
Requirement for Activation Loop Phosphorylation of the Cdc28
Cyclin-Dependent Kinase
Frederick R.
Cross* and
Kristi
Levine
The Rockefeller University, New York, New
York 10021
Received 18 December 1997/Returned for modification 13 February
1998/Accepted 23 February 1998
Many protein kinases are regulated by phosphorylation in the
activation loop, which is required for enzymatic activity. Glutamic acid can substitute for phosphothreonine in some proteins activated by
phosphorylation, but this substitution (T169E) at the site of
activation loop phosphorylation in the Saccharomyces
cerevisiae cyclin-dependent kinase (Cdk) Cdc28p blocks biological
function and protein kinase activity. Using cycles of error-prone DNA
amplification followed by selection for successively higher levels of
function, we identified mutant versions of Cdc28p-T169E with high
biological activity. The enzymatic and biological activity of the
mutant Cdc28p was essentially normally regulated by cyclin, and the
mutants supported normal cell cycle progression and regulation.
Therefore, it is not a requirement for control of the yeast cell cycle
that Cdc28p be cyclically phosphorylated and dephosphorylated. These CDC28 mutants allow viability in the absence of Cak1p, the
essential kinase that phosphorylates Cdc28p-T169, demonstrating that
T169 phosphorylation is the only essential function of Cak1p. Some growth defects remain in suppressed cak1 cdc28 strains
carrying the mutant CDC28 genes, consistent with additional
nonessential roles for CAK1.
*
Corresponding author. Mailing address: The Rockefeller
University, 1230 York Ave., New York, NY 10021. Phone: (212) 327-7685. Fax: (212) 327-7923. E-mail:
fcross{at}rockvax.rockefeller.edu.
Mol Cell Biol, May 1998, p. 2923-2931, Vol. 18, No. 5
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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