Cavallesco R, Tuan D
Harvard-MIT Division of Health Science and Technology and Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA.
Blood Cells Mol Dis. 1997;23(1):8-26. doi: 10.1006/bcmd.1997.0115.
The HS2 enhancer in the locus control region of human beta-like globin genes displays developmental-stage-independent enhancer function. The mechanism by which it regulates the transcription of the globin genes in erythroid cells throughout development is not fully understood. In this paper we dissect the HS2 enhancer into an enhancer core and five modulatory subdomains M1 to M5. The enhancer core possesses developmental-stage-independent enhancer activity. The modulatory subdomains by themselves do not possess such enhancer activity, but they apparently respond to environmental signals and modulate enhancer core activity in a developmental-stage specific manner. M1 located 5' of the core strongly stimulates core activity in K562 cells at the embryonic stage. M2 and M3 located 3' of the core strongly stimulate core activity in MEL cells at the adult stage. Moreover, M3 suppresses core activity at the embryonic stage and exhibits an adult-stage-selector activity. These findings indicate that the apparent developmental-stage-independence of the HS2 enhancer is a result of multiple interactions between the core and the modulatory subdomains located both near and far from the core.
人类β样珠蛋白基因座位控制区中的HS2增强子具有不依赖于发育阶段的增强子功能。其在整个发育过程中调控红系细胞中珠蛋白基因转录的机制尚未完全阐明。在本文中,我们将HS2增强子剖析为一个增强子核心和五个调节子域M1至M5。增强子核心具有不依赖于发育阶段的增强子活性。调节子域自身不具备这种增强子活性,但它们显然对环境信号作出反应,并以发育阶段特异性的方式调节增强子核心的活性。位于核心5'端的M1在胚胎期强烈刺激K562细胞中的核心活性。位于核心3'端的M2和M3在成年期强烈刺激MEL细胞中的核心活性。此外,M3在胚胎期抑制核心活性,并表现出成年期选择活性。这些发现表明,HS2增强子明显的发育阶段独立性是核心与位于核心附近和远处的调节子域之间多重相互作用的结果。