Lee Ming-Chia, Spradling Allan C
Howard Hughes Medical Institute Research Laboratories, Department of Embryology, Carnegie Institution, Baltimore, Maryland 21218, USA.
Howard Hughes Medical Institute Research Laboratories, Department of Embryology, Carnegie Institution, Baltimore, Maryland 21218, USA
Genes Dev. 2014 Dec 15;28(24):2739-49. doi: 10.1101/gad.252692.114.
Progenitors are early lineage cells that proliferate before the onset of terminal differentiation. Although widespread, the epigenetic mechanisms that control the progenitor state and the onset of differentiation remain elusive. By studying Drosophila ovarian follicle cell progenitors, we identified lysine-specific demethylase 1 (lsd1) and CoRest as differentiation regulators using a GAL4∷GFP variegation assay. The follicle cell progenitors in lsd1 or CoRest heterozygotes prematurely lose epigenetic plasticity, undergo the Notch-dependent mitotic-endocycle transition, and stop dividing before a normal number of follicle cells can be produced. Simultaneously reducing the dosage of the histone H3K4 methyltransferase Trithorax reverses these effects, suggesting that an Lsd1/CoRest complex times progenitor differentiation by controlling the stability of H3K4 methylation levels. Individual cells or small clones initially respond to Notch; hence, a critical level of epigenetic stabilization is acquired cell-autonomously and initiates differentiation by making progenitors responsive to pre-existing external signals.
祖细胞是在终末分化开始之前进行增殖的早期谱系细胞。尽管广泛存在,但控制祖细胞状态和分化起始的表观遗传机制仍不清楚。通过研究果蝇卵巢卵泡细胞祖细胞,我们使用GAL4∷GFP斑驳分析鉴定了赖氨酸特异性去甲基化酶1(lsd1)和CoRest作为分化调节因子。lsd1或CoRest杂合子中的卵泡细胞祖细胞过早丧失表观遗传可塑性,经历Notch依赖性的有丝分裂-内循环转变,并在产生正常数量的卵泡细胞之前停止分裂。同时降低组蛋白H3K4甲基转移酶三胸复合物的剂量可逆转这些效应,表明Lsd1/CoRest复合物通过控制H3K4甲基化水平的稳定性来调节祖细胞分化的时间。单个细胞或小克隆最初对Notch有反应;因此,表观遗传稳定的关键水平是细胞自主获得的,并通过使祖细胞对预先存在的外部信号作出反应来启动分化。