Research Topics
Genomes and Genes | Michael WeinreichSummaryAffiliation: Van Andel Research Institute Country: USA Publications
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Detail Information
Publications
The activities of eukaryotic replication origins in chromatinMichael Weinreich
Laboratory of Chromosome Replication, Van Andel Research Institute, 333 Bostwick Ave NE, Grand Rapids, MI 49503, USA
Biochim Biophys Acta 1677:142-57. 2004..These roles are not linked obligatorily to replication origin activity per se, but instead exploit multi-subunit replication proteins with the potential to form context-dependent protein-protein interactions...
An ARS element inhibits DNA replication through a SIR2-dependent mechanismAmber Crampton
Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, MI 49503, USA
Mol Cell 30:156-66. 2008..These data suggest that Sir2p and I(S) elements inhibit origin activity by promoting an unfavorable chromatin structure for pre-RC assembly...
Budding yeast Dbf4 sequences required for Cdc7 kinase activation and identification of a functional relationship between the Dbf4 and Rev1 BRCT domainsVictoria Harkins
Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, Michigan 49503, USA
Genetics 183:1269-82. 2009..Our data also suggest that the Dbf4 and Rev1 BRCT domains interact with a common protein or structure, although the precise function of both domains and their binding partners remains elusive...
High-resolution analysis of four efficient yeast replication origins reveals new insights into the ORC and putative MCM binding elementsFuJung Chang
Laboratory of Chromosome Replication, Van Andel Research Institute, 333 Bostwick Ave NE Grand Rapids, MI 49503, USA
Nucleic Acids Res 39:6523-35. 2011....
Dbf4 regulates the Cdc5 Polo-like kinase through a distinct non-canonical binding interactionYing Chou Chen
Van Andel Research Institute, Grand Rapids, Michigan 49503, USA
J Biol Chem 285:41244-54. 2010..This study, therefore, details the molecular nature of a new type of PBD binding and reveals that Cdc5 targeting to phosphorylated substrates likely regulates spindle dynamics...
A Dbf4p BRCA1 C-terminal-like domain required for the response to replication fork arrest in budding yeastCarrie Gabrielse
Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, Michigan 49503, USA
Genetics 173:541-55. 2006..Rad53p likely directly phosphorylated Dbf4p in response to RF arrest and Dbf4p was required for Rad53p abundance. Rad53p and Dbf4p therefore cooperated to coordinate a robust cellular response to RF arrest...
Analysis of chromosome III replicators reveals an unusual structure for the ARS318 silencer origin and a conserved WTW sequence within the origin recognition complex binding siteFuJung Chang
Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, MI 49503, USA
Mol Cell Biol 28:5071-81. 2008..This analysis revealed a highly conserved WTW motif 17 to 19 bp from the ACS that is functionally important and is apparent in the 228 phylogenetically conserved ARS elements among the six sensu stricto Saccharomyces species...
The NAD(+)-dependent Sir2p histone deacetylase is a negative regulator of chromosomal DNA replicationDonald L Pappas
Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, Michigan 49503, USA
Genes Dev 18:769-81. 2004....
Cdc7-Dbf4 kinase overexpression in multiple cancers and tumor cell lines is correlated with p53 inactivationDorine Bonte
Laboratories of Chromosome Replication, Van Andel Research Institute, Grand Rapids, MI 49503, USA
Neoplasia 10:920-31. 2008..6 x 10(-9) and 1.8 x 10(-10), respectively) and in the cancer cell lines we studied. Therefore, increased Cdc7-Dbf4 abundance may be a common occurrence in human malignancies...
The origin recognition complex and Sir4 protein recruit Sir1p to yeast silent chromatin through independent interactions requiring a common Sir1p domainMelissa E Bose
Department of Biomolecular Chemistry, 587 MSC, University of Wisconsin Medical School, 1300 University Avenue, Madison, WI 43706 1532, USA
Mol Cell Biol 24:774-86. 2004....
