Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2147027 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis | 2009 | 11 Pages |
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.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Cancer Research
Authors
Minoru Takata, Masamichi Ishiai, Hiroyuki Kitao,