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Molecular Cell
Article
License: Elsevier Non-Commercial
Data sources: UnpayWall
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Molecular Cell
Article . 2001
License: Elsevier Non-Commercial
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Molecular Cell
Article . 2001 . Peer-reviewed
License: Elsevier Non-Commercial
Data sources: Crossref
Molecular Cell
Article . 2002
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Human Mus81-Associated Endonuclease Cleaves Holliday Junctions In Vitro

Authors: Chen, Xiao-Bo; Melchionna, Roberta; Denis, Cecile-Marie; Gaillard, Pierre-Henri L.; Blasina, Alessandra; Van de Weyer, Inez; Boddy, Michael N.; +3 Authors

Human Mus81-Associated Endonuclease Cleaves Holliday Junctions In Vitro

Abstract

Mus81, a protein with homology to the XPF subunit of the ERCC1-XPF endonuclease, is important for replicational stress tolerance in both budding and fission yeast. Human Mus81 has associated endonuclease activity against structure-specific oligonucleotide substrates, including synthetic Holliday junctions. Mus81-associated endonuclease resolves Holliday junctions into linear duplexes by cutting across the junction exclusively on strands of like polarity. In addition, Mus81 protein abundance increases in cells following exposure to agents that block DNA replication. Taken together, these findings suggest a role for Mus81 in resolving Holliday junctions that arise when DNA replication is blocked by damage or by nucleotide depletion. Mus81 is not related by sequence to previously characterized Holliday junction resolving enzymes, and it has distinct enzymatic properties that suggest it uses a novel enzymatic strategy to cleave Holliday junctions.

Related Organizations
Keywords

DNA Replication, Saccharomyces cerevisiae Proteins, Recombinant Fusion Proteins, Molecular Sequence Data, Nuclear Proteins, Cell Biology, DNA, Endonucleases, Cell Line, DNA-Binding Proteins, Fungal Proteins, Animals, Humans, Nucleic Acid Conformation, Amino Acid Sequence, Cloning, Molecular, Molecular Biology, Sequence Alignment, DNA Damage

  • BIP!
    Impact byBIP!
    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    248
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
248
Top 10%
Top 1%
Top 1%
hybrid