Division of Oncology, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO, United States of America.
McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO, United States of America.
PLoS One. 2021 Nov 15;16(11):e0255706. doi: 10.1371/journal.pone.0255706. eCollection 2021.
Kdm6a/Utx, a gene on the X chromosome, encodes a histone H3K27me3 demethylase that has an orthologue on the Y chromosome (Uty) (Zheng et al. 2018). We previously identified inactivating mutations of Kdm6a in approximately 50% of mouse acute promyelocytic leukemia samples; however, somatic mutations of KDM6A are more rare in human AML samples, ranging in frequency from 2-15% in different series of patients, where their role in pathogenesis is not yet clear. In this study, we show that female Kdm6aflox/flox mice (with allele inactivation initiated by Vav1-Cre in hematopoietic stem and progenitor cells (HSPCs) have a sex-specific phenotype that emerges with aging, with features resembling a myelodysplastic syndrome (MDS). Female Kdm6a-knockout (KO) mice have an age-dependent expansion of their HSPCs with aberrant self-renewal, but they did not differentiate normally into downstream progeny. These mice became mildly anemic and thrombocytopenic, but did not develop overt leukemia, or die from these cytopenias. ChIP-seq and ATAC-seq studies showed only minor changes in H3K27me3, H3K27ac, H3K4me, H3K4me3 and chromatin accessibility between Kdm6a-WT and Kdm6a-KO mice. Utilizing scRNA-seq, Kdm6a loss was linked to the transcriptional repression of genes that mediate hematopoietic cell fate determination. These data demonstrate that Kdm6a plays an important role in normal hematopoiesis, and that its inactivation may contribute to AML pathogenesis.
Kdm6a/Utx 是位于 X 染色体上的一个基因,编码组蛋白 H3K27me3 去甲基化酶,在 Y 染色体上有一个同源物(Uty)(Zheng 等人,2018 年)。我们之前在大约 50%的小鼠急性早幼粒细胞白血病样本中发现了 Kdm6a 的失活突变;然而,KDM6A 的体细胞突变在人类 AML 样本中更为罕见,在不同系列的患者中频率为 2-15%,其在发病机制中的作用尚不清楚。在这项研究中,我们表明,雌性 Kdm6aflox/flox 小鼠(造血干细胞和祖细胞(HSPCs)中的 Vav1-Cre 启动等位基因失活)具有随年龄出现的性别特异性表型,其特征类似于骨髓增生异常综合征(MDS)。雌性 Kdm6a 敲除(KO)小鼠的 HSPCs 随年龄增长呈依赖性扩张,具有异常的自我更新能力,但不能正常分化为下游后代。这些小鼠出现轻度贫血和血小板减少症,但不会发展为明显的白血病,也不会因这些血细胞减少而死亡。ChIP-seq 和 ATAC-seq 研究表明,在 Kdm6a-WT 和 Kdm6a-KO 小鼠之间,H3K27me3、H3K27ac、H3K4me、H3K4me3 和染色质可及性只有微小变化。利用 scRNA-seq,Kdm6a 的缺失与介导造血细胞命运决定的基因的转录抑制有关。这些数据表明 Kdm6a 在正常造血中发挥重要作用,其失活可能导致 AML 的发病机制。