Article ID Journal Published Year Pages File Type
2147027 Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 2009 11 Pages PDF
Abstract

The Fanconi anemia (FA) pathway is a complex phosphorylation–ubiquitination network in the DNA damage signaling, which is still poorly understood. Defects in the “FA pathway” or in the related DNA repair proteins cause FA, a hereditary disorder that accompanies compromised DNA crosslink repair, poor hematopoetic stem cell survival, genomic instability, and cancer. For molecular dissection of the FA pathway, we have been using chicken B cell line DT40 as a model system. In this review, we will summarize our current understanding of the pathway, and discuss how studies using DT40 have contributed to this rapidly evolving field.

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