Howard Hughes Medical Institute and Department of Pathology, New York, New York, USA.
Nat Immunol. 2010 Mar;11(3):207-15. doi: 10.1038/ni.1839. Epub 2010 Jan 17.
Hematopoietic stem cell (HSC) differentiation is regulated by cell-intrinsic and cell-extrinsic cues. In addition to transcriptional regulation, post-translational regulation may also control HSC differentiation. To test this hypothesis, we visualized the ubiquitin-regulated protein stability of a single transcription factor, c-Myc. The stability of c-Myc protein was indicative of HSC quiescence, and c-Myc protein abundance was controlled by the ubiquitin ligase Fbw7. Fine changes in the stability of c-Myc protein regulated the HSC gene-expression signature. Using whole-genome genomic approaches, we identified specific regulators of HSC function directly controlled by c-Myc binding; however, adult HSCs and embryonic stem cells sensed and interpreted c-Myc-regulated gene expression in distinct ways. Our studies show that a ubiquitin ligase-substrate pair can orchestrate the molecular program of HSC differentiation.
造血干细胞(HSC)分化受细胞内和细胞外信号的调节。除了转录调控,翻译后调控也可能控制 HSC 分化。为了验证这一假设,我们可视化了单个转录因子 c-Myc 的泛素调节的蛋白稳定性。c-Myc 蛋白的稳定性表明 HSC 静止,c-Myc 蛋白的丰度受泛素连接酶 Fbw7 控制。c-Myc 蛋白稳定性的细微变化调节 HSC 的基因表达特征。通过全基因组基因组方法,我们鉴定了直接受 c-Myc 结合控制的 HSC 功能的特定调节剂;然而,成体 HSCs 和胚胎干细胞以不同的方式感知和解释 c-Myc 调节的基因表达。我们的研究表明,泛素连接酶-底物对可以协调 HSC 分化的分子程序。