Sunday evening |
14:00-21:00 |
Arrival & registration |
19:25-19:30 |
Opening Remarks |
19:30-21:30 |
Nucleotide Excision Repair |
This special session will open the conference for two reasons. First, NER has brought the DNA repair field to the attention of the general scientific public with the discovery of a link between UV damage repair defects and Xeroderma pigmentosum. Second, the field has now reached a stage where the repair system can be reconstituted from its individual purified recombinant components (Wood). This tour de force will be reviewed by the speakers, who all played key parts in its evolution; from the beginnings of cloning by complementation (Bootsma) through the development of a yeast (Friedberg) and in vitro (Wood) model systems to the discovery of a cross-talk between NER and transcription (Hoeijmakers). |
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Chair: Errol Friedberg (University of Texas) |
19:30-20:00 |
Errol Friedberg (University of Texas): "Recent Advances in NER in Yeast." |
20:00-20:30 |
Jan Hoeijmakers (Erasmus University, Rotterdam): "In vivo Dynamics of Nucleotide Excision Repair." |
20:30-21:00 |
Richard Wood (ICRF, London): "Nucleotide Excision Repair Enzymes in Human Cells" |
21:00-21:30 |
Discussion: Philip Hanawalt (Stanford University) |
Monday morning |
9:00-12:20 | Base-excision Repair |
The topic discussed in this section concerns the repair pathway that is of paramount importance in the removal of spontaneous DNA damage, ranging from hydrolytic deamination, through methylation to oxidative damage. The invited speakers have made major contributions to our understanding of this field. The topics discussed will cover the discovery and characterisation of BER enzymes, their mode of action based on crystal structures and role of BER in response to mutagens and stress factors. |
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Chair: Tomas Lindahl |
09:00-09:30 |
Tomas Lindahl (ICRF London): "Reconstitution and Fidelity of BER." |
09:30-10:00 |
Primo Schär (IMR Zürich): "Thymine DNA Glycosylase - Towards Unravelling of Its Physiological Role" |
10:00-10:15 |
Ashok Bhagwat (Wayne State University): "Regulation and function of E. coli Mug enzyme" |
10:15-10:45 |
Coffee break |
10:45-11:15 |
Gregory Verdine (Harvard University): "Recognition and Repair of 8-oxoguanine in Eukaryotic Cells" |
11:15-11:45 |
Bruce Demple (Harvard School of Public Health): "Regulation and Roles of AP Endonucleases." |
11:45-12:20 |
Discussion: Susan Wallace (University of Vermont) |
12:20-12:35 |
Conference photo |
Monday evening |
19:30-21:30 | Structure, Function and Fidelity of DNA Polymerases |
This session will help the participants to understand the 3D constraints that dictate replication fidelity. High resolution crystal structures of several polymerases with their respective substrates will be shown. Moreover, exciting new insights into the way these enzymes deal with damaged nucleotides will also be discussed. |
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Chair: Samuel Wilson (NIEHS) |
19:30-20:00 |
Samuel Wilson (Lab. of Struct. Biol., NIEHS, NIH): "Structure-Based Mechanisms of Nucleotide Insertion Fidelity." |
20:00-20:30 |
Sylvie Doublie (University of Vermont): "A structural
examination of fidelity in polymerases" |
20:30-21:00 |
Lorena Beese (Duke University): "Structural Analysis of
Polymerase Fidelity" |
21:00-21:30 |
Discussion: Tom Ellenberger (Harvard University) |
Tuesday morning |
9:00-12:30 | Mismatch Repair |
The session will cover the latest developments in our understanding of this important pathway, the malfunction of which is linked to hereditary nonpolyposis colon cancer. The speakers will discuss the genetics and the biochemistry of the process in systems ranging from bacteria to man. |
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Chair: Richard Kolodner (UCSD) |
09:00-09:30 |
Richard Kolodner (UCSD): "Protein-protein
interactions during mismatch repair." |
09:30-10:00 |
Eric Alani (Cornell University): "Genetic and Biochemical Analysis of Mismatch Repair Proteins in DNA Repair and Genetic Recombination." |
10:00-10:30 |
Coffee break |
10:30-11:00 |
Michael Liskay (Oregon Health Sciences University): "Mismatch Repair Functions and Cancer." |
11:00-11:30 |
Peggy Hsieh (NIH): "Mismatch Recognition by MutS: Crystal Structure of a Taq MutS-DNA Complex" |
11:30-11:45 |
Titia Sixma (Amsterdam): "The asymmetric structural heterodimer of E. coli MutS." |
11:45-12:30 |
Discussion: Thomas Kunkel (NIEHS, NIH) |
Tuesday evening |
19:30-21:30 | Genetic Instability |
Instability of repeated sequence elements is linked with several diseases ranging from triplet repeat diseases such as Fragile X Syndrome to hereditary nonpolyposis colon cancer. Sporadic cancers, also display gross genomic rearrangements. This session will aim to cover the key processes underlying these instabilities. |
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Chair: Robert Wells (Texas Medical Center) |
19:30-20:00 |
Robert Wells (Texas Medical Center): "Recombination and Repair in Genetic Instabilities of Triplet Repeat Sequences" |
20:00-20:30 |
Cynthia McMurray (Mayo Clinic): "Mutational Mechanism of Trinucleotide Expansion in Human Disease." |
20:30-21:00 |
Norman Arnheim (USC): "Trinucleotide Repeat Instability in Humans" |
21:00-21:30 |
Discussion: Robert Lahue (University of Nebraska) |
Wednesday morning |
9:00-12:30 | Double-strand Break Repair and Recombination |
Recent discoveries show that the enzymes involved in double strand break repair and in various recombination processes are identical to a large extent. This has increased our understanding of the genetic defects underlying human syndromes ranging from hypersensitivity to ionising radiation to immune deficiency. |
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Chair: Steven West (ICRF, London) |
09:00-09:30 |
Steven West (ICRF London): "Double-Strand Break Repair in Human Cells." |
09:30-10:00 |
Roland Kanaar (Erasmus University Rotterdam): "Roles of Recombination in DNA Damage Repair." |
10:00-10:30 |
Coffee break |
10:30-11:00 |
Stephen Jackson (Wellcome/CRC, Cambridge): "Signalling and Repair of DNA Double-Strand Breaks." |
11:00-11:30 |
Steven Kowalczykowski (UC Davis): "Recombination and Repair of DNA Breaks in vitro." |
11:30-12:30 |
Discussion: Susan Lees-Miller (University of Calgary) |
Wednesday evening |
19:30-21:30 | Novel DNA Polymerases in Lesion By-pass |
Bulky lesions in DNA generally block replicative polymerases. Cell death is avoided by the action of polymerases capable of bypassing the damage, either in error-free or in error-prone way. Recent months have witnessed the identification of novel enzymes, one of which (XPV) is linked to Xeroderma pigmentosum. |
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Chair: Chris Lawrence (University of Rochester) |
19:30-20:00 |
Chris Lawrence (University of Rochester): "The Role of Pol-zeta and Rev1p in Eukaryotic Mutagenesis" |
20:00-20:30 |
Roger Woodgate (NICHD, NIH): "Pol-iota, a Remarkably Error-Prone DNA Polymerase" |
20:30-21:00 |
Fumio Hanaoka (University of Osaka): "Xeroderma pigmentosum Variant Gene Encodes the Lesion Bypass DNA Polymerase (Pol-Eta)." |
21:00-21:30 |
Discussion: Myron F. Goodman (USC) |
Thursday morning |
9:00-12:30 | Cross-talk Between Diverse Pathways of DNA Metabolism |
Detailed study of several DNA repair pathways have revealed that the same enzymes are often involved in different metabolic processes. This session will discuss the common denominators in immunoglobulin gene rearrangements and double strand break repair, mismatch repair and recombination, mismatch repair and somatic hypermutation, and triplet repeat expansion and recombination. |
|
Chair: Martin Gellert (NIH) |
09:00-09:30 |
Martin Gellert (Lab of Mol. Biol., NIH): "V(D)J Recombination: Links to Transposition and Double-Strand Break Repair." |
09:30-10:00 |
Patricia Gearhart (NIA, NIH): "Hypermutation of Immunoglobulin Variable Genes in DNA Repair-Deficient Mice and Humans." |
10:00-10:30 |
Coffee break |
10:30-11:00 |
Nancy Maizels (Yale): "Conserved Enzymes and Unusual DNA Structures in Immunoglobulin Class Switch Recombination" |
11:00-11:30 |
Barbara Hohn (FMI Basel): "Recombination and Mutation in Plants." |
11:30-11:45 |
John Hayes (Oregon State University): atMSH7: A plant protein with novel mismatch-recognition properties |
11:45-12:30 |
Discussion: Rhona Borts (University of Oxford) |
Thursday evening |
19:30-21:30 | Mutagenesis in Evolution and Cancer |
Mutagenesis is generally considered to be deleterious to life. However, this process plays an important role also in evolution. The speakers in this session have made major contributions to our understanding of both these roles. |
|
Chair: Miroslav Radman (University of Paris-V) |
19:30-20:00 |
Miroslav Radman (University of Paris-V): "Sex and Stress: Genomic Non-self Recognition in Bacterial Matings" |
20:00-20:30 |
Jeffrey Miller (UCLA): "Mismatch Repair deficient mutators and their amplification in cell population" |
20:30-21:00 |
Patricia Foster (Boston U.): "Stationary-Phase Mutation in Escherichia coli." |
21:00-21:30 |
Lawrence Loeb (University of Washington) |
Friday morning |
7:30-8:30 |
Breakfast |