Alexandra M Blee, Kaitlyn S Gallagher, Hyun-Suk Kim, Mihyun Kim, Suhas S Kharat, Christina R Troll, Areetha D'Souza, Jiyoung Park, P Drew Neufer, Orlando D Schärer, Walter J Chazin
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Towards this goal, we previously developed a machine learning strategy to predict genetic variants in an essential NER protein, Xeroderma Pigmentosum Complementation Group A (XPA), that disrupt repair. In this study, we report in-depth analyses of a subset of the predicted variants, including <i>in vitro</i> analyses of purified recombinant protein and cell-based assays to test Pt agent sensitivity in cells and determine mechanisms of NER dysfunction. The most NER deficient variant Y148D had reduced protein stability, weaker DNA binding, disrupted recruitment to damage, and degradation. Our findings demonstrate that tumor mutations in XPA impact cell survival after cisplatin treatment and provide valuable mechanistic insights to improve variant effect prediction. 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引用次数: 0
摘要
核苷酸切除修复(NER)通过清除DNA中的铂病变,降低了以铂(Pt)为基础的化疗的疗效。先前的研究发现,NER基因切除修复交叉补体组1和2(ERCC1和ERCC2)的错义突变或缺失会改善患者接受铂类化疗后的疗效。虽然在患者肿瘤中发现的大多数 NER 基因改变都是错义突变,但其余近 20 个 NER 基因突变的影响尚不清楚。为了实现这一目标,我们之前开发了一种机器学习策略来预测破坏修复的重要 NER 蛋白--色素沉着病补体A组(XPA)的基因变异。在本研究中,我们报告了对预测变体子集的深入分析,包括纯化重组蛋白的体外分析和基于细胞的试验,以测试细胞对铂制剂的敏感性并确定 NER 功能障碍的机制。最缺乏 NER 的变体 Y148D 蛋白稳定性降低,DNA 结合力减弱,损伤招募和降解紊乱。我们的研究结果表明,XPA的肿瘤突变会影响细胞在顺铂治疗后的存活,并为改善变异效应预测提供了宝贵的机理见解。从广义上讲,这些发现表明在预测化疗反应时应考虑 XPA 肿瘤变异。
XPA tumor variant leads to defects in NER that sensitize cells to cisplatin.
Nucleotide excision repair (NER) reduces efficacy of treatment with platinum (Pt)-based chemotherapy by removing Pt lesions from DNA. Previous study has identified that missense mutation or loss of the NER genes Excision Repair Cross Complementation Group 1 and 2 (ERCC1 and ERCC2) leads to improved patient outcomes after treatment with Pt-based chemotherapies. Although most NER gene alterations found in patient tumors are missense mutations, the impact of mutations in the remaining nearly 20 NER genes is unknown. Towards this goal, we previously developed a machine learning strategy to predict genetic variants in an essential NER protein, Xeroderma Pigmentosum Complementation Group A (XPA), that disrupt repair. In this study, we report in-depth analyses of a subset of the predicted variants, including in vitro analyses of purified recombinant protein and cell-based assays to test Pt agent sensitivity in cells and determine mechanisms of NER dysfunction. The most NER deficient variant Y148D had reduced protein stability, weaker DNA binding, disrupted recruitment to damage, and degradation. Our findings demonstrate that tumor mutations in XPA impact cell survival after cisplatin treatment and provide valuable mechanistic insights to improve variant effect prediction. Broadly, these findings suggest XPA tumor variants should be considered when predicting chemotherapy response.