RFC1/YOR217W Literature Guide Help

Other names published for RFC1: CDC44, replication factor C subunit 1, YOR217W

RFC1 - Strains/Constructs (30)

ReferenceOther Genes Addressed
Sakato M, et al.  (2012) A central swivel point in the RFC clamp loader controls PCNA opening and loading on DNA. J Mol Biol 416(2):163-75
Svensson JP, et al.  (2011) Genomic phenotyping of the essential and non-essential yeast genome detects novel pathways for alkylation resistance. BMC Syst Biol 5(1):157
Miller A, et al.  (2010) Proliferating cell nuclear antigen (PCNA) is required for cell cycle-regulated silent chromatin on replicated and nonreplicated genes. J Biol Chem 285(45):35142-54
Moriel-Carretero M and Aguilera A  (2010) A Postincision-Deficient TFIIH Causes Replication Fork Breakage and Uncovers Alternative Rad51- or Pol32-Mediated Restart Mechanisms. Mol Cell 37(5):690-701
Chen S, et al.  (2009) Mechanism of ATP-driven PCNA clamp loading by S. cerevisiae RFC. J Mol Biol 388(3):431-42
Breslow DK, et al.  (2008) A comprehensive strategy enabling high-resolution functional analysis of the yeast genome. Nat Methods 5(8):711-8
Celic I, et al.  (2008) Histone H3 K56 hyperacetylation perturbs replisomes and causes DNA damage. Genetics 179(4):1769-84
Bylund GO, et al.  (2006) Overproduction and purification of RFC-related clamp loaders and PCNA-related clamps from Saccharomyces cerevisiae. Methods Enzymol 409():1-11
Yao NY, et al.  (2006) Mechanism of proliferating cell nuclear antigen clamp opening by replication factor C. J Biol Chem 281(25):17528-39
Franco AA, et al.  (2005) Histone deposition protein Asf1 maintains DNA replisome integrity and interacts with replication factor C. Genes Dev 19(11):1365-75
Magdalena Coman M, et al.  (2004) Dual functions, clamp opening and primer-template recognition, define a key clamp loader subunit. J Mol Biol 342(5):1457-69
Hingorani MM and Coman MM  (2002) On the specificity of interaction between the Saccharomyces cerevisiae clamp loader replication factor C and primed DNA templates during DNA replication. J Biol Chem 277(49):47213-24
Gomes XV and Burgers PM  (2001) ATP utilization by yeast replication factor C. I. ATP-mediated interaction with DNA and with proliferating cell nuclear antigen. J Biol Chem 276(37):34768-75
Gomes XV, et al.  (2001) ATP utilization by yeast replication factor C. II. Multiple stepwise ATP binding events are required to load proliferating cell nuclear antigen onto primed DNA. J Biol Chem 276(37):34776-83
Schmidt SL, et al.  (2001) ATP utilization by yeast replication factor C. III. The ATP-binding domains of Rfc2, Rfc3, and Rfc4 are essential for DNA recognition and clamp loading. J Biol Chem 276(37):34784-91
Schmidt SL, et al.  (2001) ATP utilization by yeast replication factor C. IV. RFC ATP-binding mutants show defects in DNA replication, DNA repair, and checkpoint regulation. J Biol Chem 276(37):34792-800
Beckwith W and McAlear MA  (2000) Allele-specific interactions between the yeast RFC1 and RFC5 genes suggest a basis for RFC subunit-subunit interactions. Mol Gen Genet 264(4):378-91
Gomes XV, et al.  (2000) Overproduction in Escherichia coli and characterization of yeast replication factor C lacking the ligase homology domain. J Biol Chem 275(19):14541-9
Amin NS, et al.  (1999) Dominant mutations in three different subunits of replication factor C suppress replication defects in yeast PCNA mutants. Genetics 153(4):1617-28
Ehrenhofer-Murray AE, et al.  (1999) A role for the replication proteins PCNA, RF-C, polymerase epsilon and Cdc45 in transcriptional silencing in Saccharomyces cerevisiae. Genetics 153(3):1171-82
Smith JS, et al.  (1999) A genetic screen for ribosomal DNA silencing defects identifies multiple DNA replication and chromatin-modulating factors. Mol Cell Biol 19(4):3184-97
Xie Y, et al.  (1999) Characterization of the repeat-tract instability and mutator phenotypes conferred by a Tn3 insertion in RFC1, the large subunit of the yeast clamp loader. Genetics 151(2):499-509
Beckwith WH, et al.  (1998) Destabilized PCNA trimers suppress defective Rfc1 proteins in vivo and in vitro. Biochemistry 37(11):3711-22
Noskov VN, et al.  (1998) The RFC2 gene, encoding the third-largest subunit of the replication factor C complex, is required for an S-phase checkpoint in Saccharomyces cerevisiae. Mol Cell Biol 18(8):4914-23
Gerik KJ, et al.  (1997) Overproduction and affinity purification of Saccharomyces cerevisiae replication factor C. J Biol Chem 272(2):1256-62
Galisson F and Dujon B  (1996) Sequence and analysis of a 33 kb fragment from the right arm of chromosome XV of the yeast Saccharomyces cerevisiae. Yeast 12(9):877-85
Cullmann G, et al.  (1995) Characterization of the five replication factor C genes of Saccharomyces cerevisiae. Mol Cell Biol 15(9):4661-71
Howell EA, et al.  (1994) CDC44: a putative nucleotide-binding protein required for cell cycle progression that has homology to subunits of replication factor C. Mol Cell Biol 14(1):255-67
Moir D and Botstein D  (1982) Determination of the order of gene function in the yeast nuclear division pathway using cs and ts mutants. Genetics 100(4):565-77
Moir D, et al.  (1982) Cold-sensitive cell-division-cycle mutants of yeast: isolation, properties, and pseudoreversion studies. Genetics 100(4):547-63