Department of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53705, USA.
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Development. 2020 Dec 23;147(24):dev194019. doi: 10.1242/dev.194019.
Heart regeneration in regeneration-competent organisms can be accomplished through the remodeling of gene expression in response to cardiac injury. This dynamic transcriptional response relies on the activities of tissue regeneration enhancer elements (TREEs); however, the mechanisms underlying TREEs are poorly understood. We dissected a cardiac regeneration enhancer in zebrafish to elucidate the mechanisms governing spatiotemporal gene expression during heart regeneration. Cardiac regeneration enhancer () exhibits dynamic, regeneration-dependent activity in the heart. We found that multiple injury-activated regulatory elements are distributed throughout the enhancer region. This analysis also revealed that cardiac regeneration enhancers are not only activated by injury, but surprisingly, they are also actively repressed in the absence of injury. Our data identified a short (22 bp) DNA element containing a key repressive element. Comparative analysis across species indicated that the repressive element is conserved in closely related species. The repression mechanism is not operational during embryogenesis and emerges when the heart begins to mature. Incorporating both activation and repression components into the mechanism of tissue regeneration constitutes a new paradigm that might be extrapolated to other regeneration scenarios.
在具有再生能力的生物中,心脏再生可以通过基因表达的重塑来实现,以响应心脏损伤。这种动态的转录反应依赖于组织再生增强子元件(TREEs)的活性;然而,TREEs 的机制还知之甚少。我们解析了斑马鱼中的心脏再生增强子,以阐明心脏再生过程中时空基因表达的调控机制。心脏再生增强子()在心脏中表现出动态的、再生依赖性的活性。我们发现,多个损伤激活的调控元件分布在整个增强子区域。这项分析还表明,心脏再生增强子不仅在受到损伤时被激活,而且令人惊讶的是,在没有损伤的情况下,它们也被主动抑制。我们的数据确定了一个包含关键抑制元件的短(22bp)DNA 元件。跨物种的比较分析表明,该抑制元件在亲缘关系密切的物种中是保守的。抑制机制在胚胎发生过程中不起作用,而是在心脏开始成熟时出现。将激活和抑制组件纳入组织再生机制构成了一个新的范例,可能会被推广到其他再生场景。