Abstract
Fanconi anemia (FA) is caused by mutations in 13 Fanc genes and renders cells hypersensitive to DNA interstrand cross-linking (ICL) agents. A central event in the FA pathway is mono-ubiquitylation of the FANCI-FANCD2 (ID) protein complex. Here, we characterize a previously unrecognized nuclease, Fanconi anemia-associated nuclease 1 (FAN1), that promotes ICL repair in a manner strictly dependent on its ability to accumulate at or near sites of DNA damage and that relies on mono-ubiquitylation of the ID complex. Thus, the mono-ubiquitylated ID complex recruits the downstream repair protein FAN1 and facilitates the repair of DNA interstrand cross-links.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Amino Acid Sequence
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Cell Line
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Cell Nucleus / metabolism
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DNA / metabolism*
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DNA Damage
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DNA Repair*
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Endodeoxyribonucleases
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Exodeoxyribonucleases / chemistry
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Exodeoxyribonucleases / genetics
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Exodeoxyribonucleases / metabolism*
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Fanconi Anemia Complementation Group D2 Protein / metabolism*
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Fanconi Anemia Complementation Group Proteins / metabolism*
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Gene Knockdown Techniques
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HeLa Cells
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Humans
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Mitomycin / pharmacology
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Molecular Sequence Data
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Multifunctional Enzymes
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Mutant Proteins / metabolism
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Protein Binding
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Ubiquitinated Proteins / metabolism
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Ubiquitination
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Zinc Fingers
Substances
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FANCD2 protein, human
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FANCI protein, human
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Fanconi Anemia Complementation Group D2 Protein
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Fanconi Anemia Complementation Group Proteins
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Multifunctional Enzymes
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Mutant Proteins
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Ubiquitinated Proteins
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Mitomycin
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DNA
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Endodeoxyribonucleases
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Exodeoxyribonucleases
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FAN1 protein, human