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Molecular and Cellular Biology, September 2000, p. 6390-6398, Vol. 20, No. 17
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Functional Studies on the Candidate ATPase Domains
of Saccharomyces cerevisiae MutL
Phuoc T.
Tran and
R. Michael
Liskay*
Department of Molecular and Medical Genetics,
Oregon Health Sciences University, Portland, Oregon 97201
Received 21 March 2000/Returned for modification 4 May
2000/Accepted 7 June 2000
Saccharomyces cerevisiae MutL homologues Mlh1p and
Pms1p form a heterodimer, termed MutL
, that is required for DNA
mismatch repair after mismatch binding by MutS homologues. Recent
sequence and structural studies have placed the NH2 termini
of MutL homologues in a new family of ATPases. To address the
functional significance of this putative ATPase activity in MutL
, we
mutated conserved motifs for ATP hydrolysis and ATP binding in both
Mlh1p and Pms1p and found that these changes disrupted DNA mismatch
repair in vivo. Limited proteolysis with purified recombinant MutL
demonstrated that the NH2 terminus of MutL
undergoes
conformational changes in the presence of ATP and nonhydrolyzable ATP
analogs. Furthermore, two-hybrid analysis suggested that these
ATP-binding-induced conformational changes promote an interaction
between the NH2 termini of Mlh1p and Pms1p. Surprisingly,
analysis of specific mutants suggested differential requirements for
the ATPase motifs of Mlh1p and Pms1p during DNA mismatch repair. Taken
together, these results suggest that MutL
undergoes ATP-dependent
conformational changes that may serve to coordinate downstream events
during yeast DNA mismatch repair.
*
Corresponding author. Mailing address: Department of
Molecular and Medical Genetics, Oregon Health Sciences University, 3181 SW Sam Jackson Park Rd., L103, Portland, OR 97201-3098. Phone: (503)
494-3475. Fax: (503) 494-6886. E-mail: liskaym{at}ohsu.edu.
Molecular and Cellular Biology, September 2000, p. 6390-6398, Vol. 20, No. 17
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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