School of Life Sciences, https://ror.org/03efmqc40Arizona State University, Tempe, Arizona.
Am J Physiol Cell Physiol. 2022 Nov 1;323(5):C1548-C1554. doi: 10.1152/ajpcell.00403.2022. Epub 2022 Oct 17.
The ability to regenerate tissues and organs following damage is not equally distributed across metazoans, and even highly related species can vary considerably in their regenerative capacity. Studies of animals with high regenerative potential have shown that factors expressed during normal development are often reactivated upon damage and required for successful regeneration. As such, regenerative potential may not be dictated by the presence or absence of the necessary genes, but whether such genes are appropriately activated following injury. The identification of damage-responsive enhancers that regulate regenerative gene expression in multiple species and tissues provides possible mechanistic insight into this phenomenon. Enhancers that are reused from developmental programs, and those that are potentially unique to regeneration, have been characterized individually and at a genome-wide scale. A better understanding of the regulatory events that, direct and in some cases limit, regenerative capacity is an important step in developing new methods to manipulate and augment regeneration, particularly in tissues that do not have this ability, including those of humans.
在受到损伤后能够再生组织和器官的能力在后生动物中分布并不均匀,即使是亲缘关系非常密切的物种,其再生能力也可能有很大差异。对具有高再生潜能的动物的研究表明,在正常发育过程中表达的因子在受到损伤后常常被重新激活,并对成功的再生是必需的。因此,再生潜能可能不是由必要基因的存在或缺失决定的,而是这些基因在损伤后是否被适当激活。在多种物种和组织中鉴定出对损伤有反应的增强子,这些增强子调节再生基因的表达,为这一现象提供了可能的机制见解。从发育程序中重新利用的增强子,以及那些可能是再生所特有的增强子,已经分别在基因组范围内进行了描述。更好地理解指导和限制再生能力的调控事件,是开发操纵和增强再生的新方法的重要步骤,特别是在那些不具有这种能力的组织中,包括人类的组织。