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Fanconi anemia pathway

KEGG ID: hsa03460

中文名称

Fanconi 贫血通路

通路描述

Fanconi 贫血通路对于高效修复受损 DNA 至关重要,特别是针对双链间交联(ICLs)。DNA ICL 直接被 FANCM 及其相关蛋白识别,招募 FA 核心复合物。FA 核心复合物单泛糖化 FANCD2 和 FANCI。泛糖化的 FANCD2/FANCI 成为活性形式,并与一系列 DNA 修复蛋白相互作用,促进下游修复通路。Fanconi 贫血由至少 13 个 FA 基因中的一个突变引起,其特征为先天性生长异常、骨髓衰竭和癌症易感性。
英文描述
The Fanconi anemia pathway is required for the efficient repair of damaged DNA, especially interstrand cross-links (ICLs). DNA ICL is directly recognized by FANCM and associated proteins, that recruit the FA core complex. The FA core complex monoubiquitinates FANCD2 and FANCI. The monoubiquitinated FANCD2/FANCI becomes an active form and interacts with a series of DNA repair proteins and facilitates downstream repair pathways. Fanconi anemia is caused by mutations in one of at least 13 FA genes and is characterized by congenital growth abnormalities, bone marrow failure and cancer predisposition.

所含基因

54 个基因