Activation of the FA pathway mediated by phosphorylation and ubiquitination

Masamichi Ishiai, Koichi Sato, Junya Tomida, Hiroyuki Kitao, Hitoshi Kurumizaka*, Minoru Takata


    研究成果: Article査読

    15 被引用数 (Scopus)


    Fanconi anemia (FA) is a devastating hereditary condition that impacts genome integrity, leading to clinical features such as skeletal and visceral organ malformations, attrition of bone marrow stem cells, and carcinogenesis. At least 21 proteins, when absent or defective, have been implicated in this disorder, and they together constitute the FA pathway, which functions in detection and repair of, and tolerance to, endogenous DNA damage. The damage primarily handled by the FA pathway has been assumed to be related to DNA interstrand crosslinks (ICLs). The FA pathway is activated upon ICL damage, and a hallmark of this activation is the mono-ubiquitination events of the key FANCD2-FANCI protein complex. Recent data have revealed unexpectedly complex details in the regulation of FA pathway activation by ICLs. In this short review, we summarize the knowledge accumulated over the years regarding how the FA pathway is activated via protein modifications.

    ジャーナルMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
    出版ステータスAccepted/In press - 2017 4月 14

    ASJC Scopus subject areas

    • 分子生物学
    • 遺伝学
    • 健康、毒物学および変異誘発


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