Dna2 mutants reveal interactions with Dna polymerase alpha and Ctf4, a Pol alpha accessory factor, and show that full Dna2 helicase activity is not essential for growth
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Unwinding and rewinding: double faces of helicase?Human Dna2 is a nuclear and mitochondrial DNA maintenance proteinOkazaki fragment processing-independent role for human Dna2 enzyme during DNA replicationThe alternative Ctf18-Dcc1-Ctf8-replication factor C complex required for sister chromatid cohesion loads proliferating cell nuclear antigen onto DNAMcm10 and And-1/CTF4 recruit DNA polymerase alpha to chromatin for initiation of DNA replicationEnzymatic properties of the Caenorhabditis elegans Dna2 endonuclease/helicase and a species-specific interaction between RPA and Dna2A network of multi-tasking proteins at the DNA replication fork preserves genome stabilityCross talk between the nuclease and helicase activities of Dna2: role of an essential iron-sulfur cluster domainDynamic localization of an Okazaki fragment processing protein suggests a novel role in telomere replicationIdentification of protein complexes required for efficient sister chromatid cohesion.POB3 is required for both transcription and replication in the yeast Saccharomyces cerevisiaeELG1, a yeast gene required for genome stability, forms a complex related to replication factor CSaccharomyces cerevisiae CTF18 and CTF4 are required for sister chromatid cohesionMutations in DNA replication genes reduce yeast life span.Dna2 exhibits a unique strand end-dependent helicase function.Involvement of Vts1, a structure-specific RNA-binding protein, in Okazaki fragment processing in yeast.Nuclease activity of Saccharomyces cerevisiae Dna2 inhibits its potent DNA helicase activity.An Eco1-independent sister chromatid cohesion establishment pathway in S. cerevisiae.Saccharomyces Rrm3p, a 5' to 3' DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA.Spt16-Pob3 and the HMG protein Nhp6 combine to form the nucleosome-binding factor SPN.Coordinated functions of WSS1, PSY2 and TOF1 in the DNA damage response.WDHD1 modulates the post-transcriptional step of the centromeric silencing pathwaySgs1 helicase and two nucleases Dna2 and Exo1 resect DNA double-strand break endsXenopus DNA2 is a helicase/nuclease that is found in complexes with replication proteins And-1/Ctf4 and Mcm10 and DSB response proteins Nbs1 and ATMBimodal interaction between replication-protein A and Dna2 is critical for Dna2 function both in vivo and in vitro.Replication protein A-directed unloading of PCNA by the Ctf18 cohesion establishment complex.A DNA2 Homolog Is Required for DNA Damage Repair, Cell Cycle Regulation, and Meristem Maintenance in Plants.Interplay of Mre11 nuclease with Dna2 plus Sgs1 in Rad51-dependent recombinational repair.The endonuclease activity of the yeast Dna2 enzyme is essential in vivo.Rad52/Rad59-dependent recombination as a means to rectify faulty Okazaki fragment processing.Mcl1p is a polymerase alpha replication accessory factor important for S-phase DNA damage survival.The DNA damage response pathway contributes to the stability of chromosome III derivatives lacking efficient replicators.Linking chromosome duplication and segregation via sister chromatid cohesionSchizosaccharomyces pombe pfh1+ encodes an essential 5' to 3' DNA helicase that is a member of the PIF1 subfamily of DNA helicases.Tripartite structure of Saccharomyces cerevisiae Dna2 helicase/endonucleasemcl1+, the Schizosaccharomyces pombe homologue of CTF4, is important for chromosome replication, cohesion, and segregation.Telomeres: structures in need of unwinding.Structure of the Blm10-20 S proteasome complex by cryo-electron microscopy. Insights into the mechanism of activation of mature yeast proteasomes.Genetic and functional interactions between Mus81-Mms4 and Rad27.Evidence suggesting that Pif1 helicase functions in DNA replication with the Dna2 helicase/nuclease and DNA polymerase delta
P2860
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P2860
Dna2 mutants reveal interactions with Dna polymerase alpha and Ctf4, a Pol alpha accessory factor, and show that full Dna2 helicase activity is not essential for growth
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Dna2 mutants reveal interactio ...... ty is not essential for growth
@ast
Dna2 mutants reveal interactio ...... ty is not essential for growth
@en
Dna2 mutants reveal interactio ...... y is not essential for growth.
@nl
type
label
Dna2 mutants reveal interactio ...... ty is not essential for growth
@ast
Dna2 mutants reveal interactio ...... ty is not essential for growth
@en
Dna2 mutants reveal interactio ...... y is not essential for growth.
@nl
altLabel
Dna2 mutants reveal interactio ...... ty is not essential for growth
@en
prefLabel
Dna2 mutants reveal interactio ...... ty is not essential for growth
@ast
Dna2 mutants reveal interactio ...... ty is not essential for growth
@en
Dna2 mutants reveal interactio ...... y is not essential for growth.
@nl
P2860
P3181
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P1476
Dna2 mutants reveal interactio ...... ty is not essential for growth
@en
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P577
1999-04-01T00:00:00Z