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碱基切除修复蛋白在复制应激诱导的 MLL 不稳定期间将激活诱导的胞嘧啶脱氨酶和内切酶 G 偶联。

Base excision repair proteins couple activation-induced cytidine deaminase and endonuclease G during replication stress-induced MLL destabilization.

机构信息

Gynaecological Oncology, Department of Obstetrics and Gynaecology, Ulm University, Ulm, Germany.

出版信息

Leukemia. 2018 Jan;32(1):159-167. doi: 10.1038/leu.2017.191. Epub 2017 Jun 19.

Abstract

The breakpoint cluster region of the MLL gene (MLLbcr) is frequently rearranged in therapy-related and infant acute leukaemia, but the destabilizing mechanism is poorly understood. We recently proposed that DNA replication stress results in MLLbcr cleavage via endonuclease G (EndoG) and represents the common denominator of genotoxic therapy-induced MLL destabilization. Here we performed a siRNA screen for new factors involved in replication stress-induced MLL rearrangements employing an enhanced green fluorescent protein-based reporter system. We identified 10 factors acting in line with EndoG in MLLbcr breakage or further downstream in the repair of the MLLbcr breaks, including activation-induced cytidine deaminase (AID), previously proposed to initiate MLLbcr rearrangements in an RNA transcription-dependent mechanism. Further analysis connected AID and EndoG in MLLbcr destabilization via base excision repair (BER) components. We show that replication stress-induced recruitment of EndoG to the MLLbcr and cleavage are AID/BER dependent. Notably, inhibition of the core BER factor Apurinic-apyrimidinic endonuclease 1 protects against MLLbcr cleavage in tumour and human cord blood-derived haematopoietic stem/progenitor cells, harbouring the cells of origin of leukaemia. We propose that off-target binding of AID to the MLLbcr initiates BER-mediated single-stranded DNA cleavage, which causes derailed EndoG activity ultimately resulting in leukaemogenic MLLbcr rearrangements.

摘要

MLL 基因(MLLbcr)的断点簇区经常在治疗相关和婴儿急性白血病中发生重排,但破坏稳定的机制尚不清楚。我们最近提出,DNA 复制应激通过内切酶 G(EndoG)导致 MLLbcr 切割,这是遗传毒性治疗诱导的 MLL 破坏的共同因素。在这里,我们使用增强型绿色荧光蛋白(EGFP)报告系统,进行了 siRNA 筛选,以寻找新的参与复制应激诱导的 MLL 重排的因素。我们确定了 10 个因子,这些因子在 MLLbcr 断裂处的断裂或修复过程中与 EndoG 作用一致,包括激活诱导的胞嘧啶脱氨酶(AID),先前提出的该酶通过 RNA 转录依赖性机制引发 MLLbcr 重排。进一步的分析将 AID 和 EndoG 连接在 MLLbcr 破坏的过程中,通过碱基切除修复(BER)的组成部分。我们表明,复制应激诱导的 EndoG 募集到 MLLbcr 并发生切割依赖于 AID/BER。值得注意的是,抑制核心 BER 因子脱嘌呤脱嘧啶内切酶 1(APE1)可防止肿瘤和人脐带血来源的造血干/祖细胞中的 MLLbcr 切割,这些细胞是白血病的起源细胞。我们提出,AID 对 MLLbcr 的非靶标结合启动了 BER 介导的单链 DNA 切割,导致 EndoG 活性失控,最终导致致白血病的 MLLbcr 重排。

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