FANCD2 相关核酸酶 KIAA1018/FAN1 的缺乏使细胞对链间交联剂敏感。
Deficiency of FANCD2-associated nuclease KIAA1018/FAN1 sensitizes cells to interstrand crosslinking agents.
机构信息
Institute of Molecular Cancer Research, University of Zurich, ETH Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
出版信息
Cell. 2010 Jul 9;142(1):77-88. doi: 10.1016/j.cell.2010.06.022.
Cytotoxicity of cisplatin and mitomycin C (MMC) is ascribed largely to their ability to generate interstrand crosslinks (ICLs) in DNA, which block the progression of replication forks. The processing of ICLs requires the Fanconi anemia (FA) pathway, excision repair, and translesion DNA synthesis (TLS). It also requires homologous recombination (HR), which repairs double-strand breaks (DSBs) generated by cleavage of the blocked replication forks. Here we describe KIAA1018, an evolutionarily conserved protein that has an N-terminal ubiquitin-binding zinc finger (UBZ) and a C-terminal nuclease domain. KIAA1018 is a 5'-->3' exonuclease and a structure-specific endonuclease that preferentially incises 5' flaps. Like cells from FA patients, human cells depleted of KIAA1018 are sensitized to ICL-inducing agents and display chromosomal instability. The link of KIAA1018 to the FA pathway is further strengthened by its recruitment to DNA damage through interaction of its UBZ domain with monoubiquitylated FANCD2. We therefore propose to name KIAA1018 FANCD2-associated nuclease, FAN1.
顺铂和丝裂霉素 C(MMC)的细胞毒性主要归因于它们在 DNA 中生成链间交联(ICLs)的能力,这些交联会阻止复制叉的前进。ICLs 的处理需要范可尼贫血(FA)途径、切除修复和跨损伤 DNA 合成(TLS)。它还需要同源重组(HR),HR 修复由受阻的复制叉切割产生的双链断裂(DSBs)。在这里,我们描述了 KIAA1018,这是一种进化上保守的蛋白,具有 N 端泛素结合锌指(UBZ)和 C 端核酸酶结构域。KIAA1018 是一种 5'->3'外切核酸酶和结构特异性内切核酸酶,优先切割 5' 发夹。与 FA 患者的细胞一样,耗尽 KIAA1018 的人细胞对 ICL 诱导剂敏感,并表现出染色体不稳定。KIAA1018 通过其 UBZ 结构域与单泛素化的 FANCD2 相互作用被募集到 DNA 损伤部位,这进一步加强了它与 FA 途径的联系。因此,我们建议将 KIAA1018 命名为 FANCD2 相关核酸酶,FAN1。