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Developmental Cell
Article
License: Elsevier Non-Commercial
Data sources: UnpayWall
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Developmental Cell
Article . 2009
License: Elsevier Non-Commercial
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Developmental Cell
Article . 2009 . Peer-reviewed
License: Elsevier Non-Commercial
Data sources: Crossref
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Inactivation of Murine Usp1 Results in Genomic Instability and a Fanconi Anemia Phenotype

Authors: Kim, Jung Min; Parmar, Kalindi; Huang, Min; Weinstock, David M.; Ruit, Carrie Ann; Kutok, Jeffrey L.; D'Andrea, Alan D.;

Inactivation of Murine Usp1 Results in Genomic Instability and a Fanconi Anemia Phenotype

Abstract

Fanconi anemia (FA) is a human genetic disease characterized by chromosome instability, cancer predisposition, and cellular hypersensitivity to DNA crosslinking agents. The FA pathway regulates the repair of DNA crosslinks. A critical step in this pathway is the monoubiquitination and deubiquitination of FANCD2. Deubiquitination of FANCD2 is mediated by the ubiquitin protease, USP1. Here, we demonstrate that targeted deletion of mouse Usp1 results in elevated perinatal lethality, male infertility, crosslinker hypersensitivity, and an FA phenotype. Usp1(-/-) mouse embryonic fibroblasts had heightened levels of monoubiquitinated Fancd2 in chromatin. Usp1(-/-) cells exhibited impaired Fancd2 foci assembly and a defect in homologous recombination repair. Double knockout of Usp1 and Fancd2 resulted in a more severe phenotype than either single knockout. Our results indicate that mouse Usp1 functions downstream in the FA pathway. Deubiquitination is a critical event required for Fancd2 nuclear foci assembly, release from chromatin, and function in DNA repair.

Related Organizations
Keywords

Male, Mice, Knockout, DNA Repair, PROTEINS, Arabidopsis Proteins, Fanconi Anemia Complementation Group D2 Protein, DEVBIO, CELLCYCLE, Fibroblasts, Genomic Instability, Mice, Fanconi Anemia, Phenotype, Endopeptidases, Animals, Female, Lymphocytes, Ubiquitin-Specific Proteases, Crosses, Genetic, Gene Deletion, Developmental Biology

  • BIP!
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    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).
    225
    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 1%
    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 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
Powered by OpenAIRE graph
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!
225
Top 1%
Top 10%
Top 1%
hybrid