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复发性非编码性体细胞和种系 WT1 变异体趋于破坏急性早幼粒细胞白血病中的 MYB 结合。

Recurrent noncoding somatic and germline WT1 variants converge to disrupt MYB binding in acute promyelocytic leukemia.

机构信息

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.

School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Blood. 2022 Sep 8;140(10):1132-1144. doi: 10.1182/blood.2021014945.

Abstract

Genetic alternations can occur at noncoding regions, but how they contribute to cancer pathogenesis is poorly understood. Here, we established a mutational landscape of cis-regulatory regions (CREs) in acute promyelocytic leukemia (APL) based on whole-genome sequencing analysis of paired tumor and germline samples from 24 patients and epigenetic profiling of 16 patients. Mutations occurring in CREs occur preferentially in active enhancers bound by the complex of master transcription factors in APL. Among significantly enriched mutated CREs, we found a recurrently mutated region located within the third intron of WT1, an essential regulator of normal and malignant hematopoiesis. Focusing on noncoding mutations within this WT1 intron, an analysis on 169 APL patients revealed that somatic mutations were clustered into a focal hotspot region, including one site identified as a germline polymorphism contributing to APL risk. Significantly decreased WT1 expression was observed in APL patients bearing somatic and/or germline noncoding WT1 variants. Furthermore, biallelic WT1 inactivation was recurrently found in APL patients with noncoding WT1 variants, which resulted in the complete loss of WT1. The high incidence of biallelic inactivation suggested the tumor suppressor activity of WT1 in APL. Mechanistically, noncoding WT1 variants disrupted MYB binding on chromatin and suppressed the enhancer activity and WT1 expression through destroying the chromatin looping formation. Our study highlights the important role of noncoding variants in the leukemogenesis of APL.

摘要

遗传改变可能发生在非编码区域,但它们如何导致癌症发病机制尚不清楚。在这里,我们基于 24 名患者的肿瘤和种系配对样本的全基因组测序分析以及 16 名患者的表观遗传谱分析,建立了急性早幼粒细胞白血病 (APL) 的顺式调控区 (CRE) 的突变景观。发生在 CRE 中的突变优先发生在 APL 中由主转录因子复合物结合的活性增强子中。在显著富集的突变 CRE 中,我们发现了一个位于 WT1 第三个内含子内的反复突变区域,WT1 是正常和恶性造血的重要调节因子。聚焦于该 WT1 内含子中的非编码突变,对 169 名 APL 患者的分析表明,体细胞突变聚集在一个焦点热点区域,包括一个被确定为导致 APL 风险的种系多态性的位点。在携带体细胞和/或种系非编码 WT1 变体的 APL 患者中观察到 WT1 表达明显降低。此外,非编码 WT1 变体在 APL 患者中反复发现 WT1 双等位基因失活,导致 WT1 完全缺失。WT1 双等位基因失活的高发生率表明 WT1 在 APL 中的肿瘤抑制活性。从机制上讲,非编码 WT1 变体破坏了染色质上的 MYB 结合,并通过破坏染色质环形成抑制了增强子活性和 WT1 表达。我们的研究强调了非编码变异在 APL 白血病发生中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cbe/9461475/3c070b9b5927/bloodBLD2021014945absf1.jpg

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