Department of Medical and Clinical Genetics, University of Helsinki, FI-00014, Helsinki, Finland.
Genome-Scale Biology, Research Programs Unit, University of Helsinki, FI-00014, Helsinki, Finland.
Nat Commun. 2019 Mar 19;10(1):1252. doi: 10.1038/s41467-019-09198-7.
Clonal hematopoiesis driven by somatic heterozygous TET2 loss is linked to malignant degeneration via consequent aberrant DNA methylation, and possibly to cardiovascular disease via increased cytokine and chemokine expression as reported in mice. Here, we discover a germline TET2 mutation in a lymphoma family. We observe neither unusual predisposition to atherosclerosis nor abnormal pro-inflammatory cytokine or chemokine expression. The latter finding is confirmed in cells from three additional unrelated TET2 germline mutation carriers. The TET2 defect elevates blood DNA methylation levels, especially at active enhancers and cell-type specific regulatory regions with binding sequences of master transcription factors involved in hematopoiesis. The regions display reduced methylation relative to all open chromatin regions in four DNMT3A germline mutation carriers, potentially due to TET2-mediated oxidation. Our findings provide insight into the interplay between epigenetic modulators and transcription factor activity in hematological neoplasia, but do not confirm the putative role of TET2 in atherosclerosis.
由体细胞杂合性 TET2 缺失驱动的克隆性造血与恶性转化有关,这是通过随后的异常 DNA 甲基化引起的,并且如在小鼠中所报道的那样,可能通过增加细胞因子和趋化因子的表达与心血管疾病有关。在这里,我们在一个淋巴瘤家族中发现了一个种系 TET2 突变。我们既没有观察到动脉粥样硬化的异常易感性,也没有观察到异常的促炎细胞因子或趋化因子表达。这一发现在另外三个无关的 TET2 种系突变携带者的细胞中得到了证实。TET2 缺陷会升高血液 DNA 甲基化水平,尤其是在活性增强子和与造血相关的主转录因子结合序列的细胞类型特异性调节区域。与四个 DNMT3A 种系突变携带者的所有开放染色质区域相比,这些区域的甲基化水平降低,这可能是由于 TET2 介导的氧化。我们的研究结果提供了对血液恶性肿瘤中表观遗传调节剂和转录因子活性相互作用的深入了解,但不能证实 TET2 在动脉粥样硬化中的假定作用。