Division of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
1] Division of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA [2] Driskill Graduate Program in Life Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Oncogene. 2014 Jun 12;33(24):3161-71. doi: 10.1038/onc.2013.289. Epub 2013 Jul 22.
The mechanisms that coordinate the final mitotic divisions of terminally differentiated bone marrow (BM) erythroid cells with components of their structural and functional maturation program remain largely undefined. We previously identified phenotypes resembling those found in early-stage myelodysplastic syndromes (MDS), including ineffective erythropoiesis, morphologic dysplasia and BM hyper-cellularity, in a knock-in mouse model in which cyclin E mutations were introduced at its two Cdc4 phosphodegrons (CPDs) to ablate Fbw7-dependent ubiquitination and degradation. Here, we have examined the physiologic consequences of cyclin E dysregulation in BM erythroid cells during terminal maturation in vivo. We found that cyclin E protein levels in BM erythroid cells are dynamically regulated in a CPD-dependent manner and that disruption of Fbw7-dependent cyclin E regulation impairs terminal erythroid cell maturation at a discrete stage before enucleation. At this stage of erythroid cell maturation, CPD phosphorylation of cyclin E regulates both cell-cycle arrest and survival. We also found that normal regulation of cyclin E restrains mitochondrial reactive oxygen species (ROS) accumulation and expression of genes that promote mitochondrial biogenesis and oxidative metabolism during terminal erythroid maturation. In the setting of dysregulated cyclin E expression, p53 is activated in BM erythroid cells as part of a DNA damage response-type pathway, which mitigates ineffective erythropoiesis, in contrast to the role of p53 induction in other models of dyserythropoiesis. Finally, cyclin E dysregulation and ROS accumulation induce histone H3 lysine 9 hyper-methylation and disrupt components of the normal terminal erythroid maturation gene expression program. Thus, ubiquitin-proteasome pathway control of G1-to-S-phase progression is intrinsically linked to regulation of metabolism and gene expression in terminally differentiating BM erythroid cells.
协调终末分化骨髓(BM)红细胞与结构和功能成熟程序组件的最后有丝分裂分裂的机制在很大程度上仍未定义。我们之前在一个敲入小鼠模型中发现了类似于早期骨髓增生异常综合征(MDS)的表型,包括无效红细胞生成、形态发育不良和 BM 细胞过度增生,其中 cyclin E 突变被引入其两个 Cdc4 磷酸降解区(CPD)以消除 Fbw7 依赖性泛素化和降解。在这里,我们研究了体内终末成熟过程中 BM 红细胞中环化酶 E 失调的生理后果。我们发现,BM 红细胞中环化酶 E 蛋白水平以 CPD 依赖性方式动态调节,并且破坏 Fbw7 依赖性 cyclin E 调节会在去核前的离散阶段损害终末红细胞成熟。在红细胞成熟的这个阶段,CPD 磷酸化的 cyclin E 调节细胞周期停滞和存活。我们还发现,cyclin E 的正常调节可抑制线粒体活性氧(ROS)积累,并在终末红细胞成熟过程中抑制促进线粒体生物发生和氧化代谢的基因表达。在 cyclin E 表达失调的情况下,p53 作为 DNA 损伤反应型途径的一部分在 BM 红细胞中被激活,这减轻了无效红细胞生成,与其他红细胞生成异常模型中 p53 诱导的作用相反。最后,cyclin E 失调和 ROS 积累诱导组蛋白 H3 赖氨酸 9 超甲基化,并破坏正常终末红细胞成熟基因表达程序的成分。因此,G1 期到 S 期进展的泛素-蛋白酶体途径控制与代谢和终末分化 BM 红细胞中的基因表达调控内在相关。