Institut de Biochimie et Génétique Cellulaires, CNRS, UMR 5095, Université de Bordeaux, F-33000 Bordeaux, France.
CNRS, IMN, UMR 5293, Université de Bordeaux, F-33000 Bordeaux, France.
Cells. 2023 Sep 28;12(19):2379. doi: 10.3390/cells12192379.
Purines are required for fundamental biological processes and alterations in their metabolism lead to severe genetic diseases associated with developmental defects whose etiology remains unclear. Here, we studied the developmental requirements for purine metabolism using the amphibian as a vertebrate model. We provide the first functional characterization of purine pathway genes and show that these genes are mainly expressed in nervous and muscular embryonic tissues. Morphants were generated to decipher the functions of these genes, with a focus on the adenylosuccinate lyase (), which is an enzyme required for both salvage and de novo purine pathways. knockdown led to a severe reduction in the expression of the myogenic regulatory factors (MRFs: Myod1, Myf5 and Myogenin), thus resulting in defects in somite formation and, at later stages, the development and/or migration of both craniofacial and hypaxial muscle progenitors. The reduced expressions of and , which are two genes specific to the salvage and de novo pathways, respectively, resulted in similar alterations. In conclusion, our data show for the first time that de novo and recycling purine pathways are essential for myogenesis and highlight new mechanisms in the regulation of MRF gene expression.
嘌呤是基本生物过程所必需的,其代谢的改变会导致与发育缺陷相关的严重遗传疾病,其病因尚不清楚。在这里,我们使用两栖动物作为脊椎动物模型来研究嘌呤代谢的发育需求。我们首次对嘌呤途径基因进行了功能表征,并表明这些基因主要在神经和肌肉胚胎组织中表达。生成了形态发生体来破译这些基因的功能,重点是腺嘌呤琥珀酸裂解酶(),它是补救和从头合成嘌呤途径所必需的酶。的敲低导致肌生成调节因子(MRFs:Myod1、Myf5 和 Myogenin)的表达严重减少,从而导致体节形成缺陷,并且在后期,颅面和轴下肌肉祖细胞的发育和/或迁移也受到影响。分别针对补救和从头合成途径特异性的基因和的表达减少导致了类似的改变。总之,我们的数据首次表明,从头合成和回收嘌呤途径对于肌发生是必不可少的,并强调了 MRF 基因表达调控的新机制。