Mismatch repair plays a key role in genetic stabilization, with inactivation of the human pathway being the cause of several forms of cancer. This system has been conserved during evolution, and the E. coil methyl-directed reaction has served as the paradigm for study of the reaction in higher cells. Although bacterial mismatch repair has been reconstituted in a pure system, numerous questions remain concerning the mechanism of the reaction. This proposal addresses several of these issues. Mismatch recognition by MutS is responsible for initiation of repair, but function of the MutS ATPase is poorly understood. Using substrate binding and pre-steady-state kinetic methods, we will further clarify the nature of the interactions between the MutS nucleotide and DNA binding centers. A number of multiprotein.DNA assemblies have been implicated in mismatch repair, but the molecular nature of the MutL.MutS, MutH.MutL.MutS, and DNA helicase II.MutL.MutS complexes remains undefined. A second goal of this project is to establish the nature of these multi-protein DNA assemblies. This phase of the work will also address the significance of the specific interaction between the beta replication clamp and MutS. Since this interaction may be indicative of a special affiliation of the mismatch repair system with the replication apparatus, we will test the clamp loader and the beta clamp for potential modulatory effects on the initiation and excision steps of mismatch repair, and assess potential regulatory effects of MutS, MutL, and other repair proteins on the elongation activity of DNA polymerase III holoenzyme in response to presence of a mismatch within the primer-template. Basic features of the excision step of mismatch repair have been established, but the mechanism that underlies this bidirectional reaction is not understood.
The third aim of this project is to further clarify the molecular details of this complex reaction with respect to intermediates, recycling of repair activities, and the basis of excision termination upon mismatch removal.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM023719-30
Application #
6917803
Study Section
Biochemistry Study Section (BIO)
Program Officer
Portnoy, Matthew
Project Start
1977-08-01
Project End
2008-07-31
Budget Start
2005-08-01
Budget End
2006-07-31
Support Year
30
Fiscal Year
2005
Total Cost
$445,115
Indirect Cost
Name
Duke University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Modrich, Paul (2016) Mechanisms in E. coli and Human Mismatch Repair (Nobel Lecture). Angew Chem Int Ed Engl 55:8490-501
Pluciennik, Anna; Burdett, Vickers; Lukianova, Olga et al. (2009) Involvement of the beta clamp in methyl-directed mismatch repair in vitro. J Biol Chem 284:32782-91
Pluciennik, Anna; Modrich, Paul (2007) Protein roadblocks and helix discontinuities are barriers to the initiation of mismatch repair. Proc Natl Acad Sci U S A 104:12709-13
Lopez de Saro, Francisco J; Marinus, Martin G; Modrich, Paul et al. (2006) The beta sliding clamp binds to multiple sites within MutL and MutS. J Biol Chem 281:14340-9
Iyer, Ravi R; Pluciennik, Anna; Burdett, Vickers et al. (2006) DNA mismatch repair: functions and mechanisms. Chem Rev 106:302-23
Bjornson, Keith P; Blackwell, Leonard J; Sage, Harvey et al. (2003) Assembly and molecular activities of the MutS tetramer. J Biol Chem 278:34667-73
Bjornson, Keith P; Modrich, Paul (2003) Differential and simultaneous adenosine di- and triphosphate binding by MutS. J Biol Chem 278:18557-62
Baitinger, Celia; Burdett, Vickers; Modrich, Paul (2003) Hydrolytically deficient MutS E694A is defective in the MutL-dependent activation of MutH and in the mismatch-dependent assembly of the MutS.MutL.heteroduplex complex. J Biol Chem 278:49505-11
Blackwell, L J; Bjornson, K P; Allen, D J et al. (2001) Distinct MutS DNA-binding modes that are differentially modulated by ATP binding and hydrolysis. J Biol Chem 276:34339-47
Burdett, V; Baitinger, C; Viswanathan, M et al. (2001) In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair. Proc Natl Acad Sci U S A 98:6765-70

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