Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2011-5-10
pubmed:abstractText
The facilitates chromatin transcription (FACT) complex affects nuclear DNA transactions in a chromatin context. Though the involvement of FACT in eukaryotic DNA replication has been revealed, a clear understanding of its biochemical behavior during DNA replication still remains elusive. Here, we analyzed the chromatin-binding dynamics of FACT using Xenopus egg extract cell-free system. We found that FACT has at least two distinct chromatin-binding phases: (1) a rapid chromatin-binding phase at the onset of DNA replication that did not involve origin licensing and (2) a second phase of chromatin binding that initiated after origin licensing. Intriguingly, early-binding FACT dissociated from chromatin when DNA replication was blocked by the addition of Cdc6 in the licensed state before origin firing. Cdc6-induced removal of FACT was blocked by the inhibition of origin licensing with geminin, but not by suppressing the activity of DNA polymerases, CDK, or Cdc7. Furthermore, chromatin transfer experiments revealed that impairing the later binding of FACT severely compromises DNA replication activity. Taken together, we propose that even though FACT has rapid chromatin-binding activity, the binding pattern of FACT on chromatin changes after origin licensing, which may contribute to the establishment of its functional link to the DNA replication machinery.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0006-3002
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 Elsevier B.V. All rights reserved.
pubmed:issnType
Print
pubmed:volume
1813
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1129-36
pubmed:meshHeading
pubmed-meshheading:21232560-Animals, pubmed-meshheading:21232560-Cell Cycle Proteins, pubmed-meshheading:21232560-Chromatin, pubmed-meshheading:21232560-DNA Replication, pubmed-meshheading:21232560-DNA-Binding Proteins, pubmed-meshheading:21232560-Eukaryotic Cells, pubmed-meshheading:21232560-Female, pubmed-meshheading:21232560-Glutathione Transferase, pubmed-meshheading:21232560-High Mobility Group Proteins, pubmed-meshheading:21232560-Histone Chaperones, pubmed-meshheading:21232560-Humans, pubmed-meshheading:21232560-Immunoblotting, pubmed-meshheading:21232560-Kinetics, pubmed-meshheading:21232560-Male, pubmed-meshheading:21232560-Nuclear Proteins, pubmed-meshheading:21232560-Oocytes, pubmed-meshheading:21232560-Protein Binding, pubmed-meshheading:21232560-Spermatozoa, pubmed-meshheading:21232560-Time Factors, pubmed-meshheading:21232560-Transcriptional Elongation Factors, pubmed-meshheading:21232560-Xenopus laevis
pubmed:year
2011
pubmed:articleTitle
Biphasic chromatin binding of histone chaperone FACT during eukaryotic chromatin DNA replication.
pubmed:affiliation
Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't