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The Fanconi anemia pathway in replication stress and DNA crosslink repair.


ABSTRACT: Interstand crosslinks (ICLs) are DNA lesions where the bases of opposing DNA strands are covalently linked, inhibiting critical cellular processes such as transcription and replication. Chemical agents that generate ICLs cause chromosomal abnormalities including breaks, deletions and rearrangements, making them highly genotoxic compounds. This toxicity has proven useful for chemotherapeutic treatment against a wide variety of cancer types. The majority of our understanding of ICL repair in humans has been uncovered through analysis of the rare genetic disorder Fanconi anemia, in which patients are extremely sensitive to crosslinking agents. Here, we discuss recent insights into ICL repair gained using new repair assays and highlight the role of the Fanconi anemia repair pathway during replication stress.

SUBMITTER: Jones MJ 

PROVIDER: S-EPMC3890373 | biostudies-literature | 2012 Dec

REPOSITORIES: biostudies-literature

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The Fanconi anemia pathway in replication stress and DNA crosslink repair.

Jones Mathew J K MJ   Huang Tony T TT  

Cellular and molecular life sciences : CMLS 20120629 23


Interstand crosslinks (ICLs) are DNA lesions where the bases of opposing DNA strands are covalently linked, inhibiting critical cellular processes such as transcription and replication. Chemical agents that generate ICLs cause chromosomal abnormalities including breaks, deletions and rearrangements, making them highly genotoxic compounds. This toxicity has proven useful for chemotherapeutic treatment against a wide variety of cancer types. The majority of our understanding of ICL repair in human  ...[more]

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