Department of Anatomy, Faculty of Medicine, 37251 Jordan University of Science & Technology , Irbid 22110, Jordan.
Exp Biol Med (Maywood). 2018 Jan;243(2):118-128. doi: 10.1177/1535370217749494. Epub 2018 Jan 7.
Prenatal and postnatal myogenesis share many cellular and molecular aspects. Myogenic regulatory factors are basic Helix-Loop-Helix transcription factors that indispensably regulate both processes. These factors (Myf5, MyoD, Myogenin, and MRF4) function as an orchestrating cascade, with some overlapped actions. Prenatally, myogenic regulatory factors are restrictedly expressed in somite-derived myogenic progenitor cells and their derived myoblasts. Postnatally, myogenic regulatory factors are important in regulating the myogenesis process via satellite cells. Many positive and negative regulatory mechanisms exist either between myogenic regulatory factors themselves or between myogenic regulatory factors and other proteins. Upstream factors and signals are also involved in the control of myogenic regulatory factors expression within different prenatal and postnatal myogenic cells. Here, the authors have conducted a thorough and an up-to-date review of the myogenic regulatory factors since their discovery 30 years ago. This review discusses the myogenic regulatory factors structure, mechanism of action, and roles and regulations during prenatal and postnatal myogenesis. Impact statement Myogenic regulatory factors (MRFs) are key players in the process of myogenesis. Despite a considerable amount of literature regarding these factors, their exact mechanisms of actions are still incompletely understood with several overlapped functions. Herein, we revised what has hitherto been reported in the literature regarding MRF structures, molecular pathways that regulate their activities, and their roles during pre- and post-natal myogenesis. The work submitted in this review article is considered of great importance for researchers in the field of skeletal muscle formation and regeneration, as it provides a comprehensive summary of all the biological aspects of MRFs and advances a better understanding of the cellular and molecular mechanisms regulating myogenesis. Indeed, attaining a better understanding of MRFs could be utilized in developing novel therapeutic protocols for multiple myopathies.
产前和产后的肌发生有许多细胞和分子方面的共同之处。肌生成调节因子是基本螺旋-环-螺旋转录因子,对这两个过程都不可或缺地进行调节。这些因子(Myf5、MyoD、Myogenin 和 MRF4)作为一个协调级联发挥作用,具有一些重叠的作用。在产前,肌生成调节因子在体节衍生的肌源性祖细胞及其衍生的成肌细胞中受到限制表达。在产后,肌生成调节因子通过卫星细胞在调节肌发生过程中很重要。在肌生成调节因子本身之间或在肌生成调节因子和其他蛋白质之间存在许多正、负调节机制。上游因子和信号也参与不同产前和产后肌源性细胞中肌生成调节因子表达的控制。在这里,作者对 30 年前发现的肌生成调节因子进行了全面和最新的综述。这篇综述讨论了肌生成调节因子的结构、作用机制以及在产前和产后肌发生中的作用和调节。
影响说明
肌生成调节因子(MRFs)是肌发生过程中的关键参与者。尽管有相当多的关于这些因子的文献,但它们的确切作用机制仍不完全清楚,存在几个重叠的功能。本文综述了迄今为止关于 MRF 结构、调节其活性的分子途径以及它们在产前和产后肌发生中的作用的文献报道。本文综述中提交的工作被认为对骨骼肌形成和再生领域的研究人员非常重要,因为它全面总结了 MRF 的所有生物学方面,并深入了解了调节肌发生的细胞和分子机制。实际上,更好地理解 MRFs 可以用于开发多种肌病的新治疗方案。