Lienkamp Soeren S
Renal Division, Department of Medicine, University of Freiburg Medical Center, Hugstetter Straße 55, 79106 Freiburg, Germany; Center for Biological Signaling Studies (BIOSS), Albertstraße 19, 79104 Freiburg, Germany.
Semin Cell Dev Biol. 2016 Mar;51:117-24. doi: 10.1016/j.semcdb.2016.02.002. Epub 2016 Feb 3.
Modern sequencing technology is revolutionizing our knowledge of inherited kidney disease. However, the molecular role of genes affected by the rapidly rising number of identified mutations is lagging behind. Xenopus is a highly useful, but underutilized model organism with unique properties excellently suited to decipher the molecular mechanisms of kidney development and disease. The embryonic kidney (pronephros) can be manipulated on only one side of the animal and its formation observed directly through the translucent skin. The moderate evolutionary distance between Xenopus and humans is a huge advantage for studying basic principles of kidney development, but still allows us to analyze the function of disease related genes. Optogenetic manipulations and genome editing by CRISPR/Cas are exciting additions to the toolbox for disease modelling and will facilitate the use of Xenopus in translational research. Therefore, the future of Xenopus in kidney research is bright.
现代测序技术正在彻底改变我们对遗传性肾病的认识。然而,受迅速增加的已鉴定突变影响的基因的分子作用仍滞后。非洲爪蟾是一种非常有用但未得到充分利用的模式生物,具有独特的特性,非常适合用于解读肾脏发育和疾病的分子机制。胚胎肾(前肾)可以在动物的一侧进行操作,并通过半透明的皮肤直接观察其形成过程。非洲爪蟾与人类之间适度的进化距离对于研究肾脏发育的基本原理是一个巨大优势,但这仍使我们能够分析疾病相关基因的功能。光遗传学操作和CRISPR/Cas介导的基因组编辑是疾病建模工具箱中令人兴奋的补充,将促进非洲爪蟾在转化研究中的应用。因此,非洲爪蟾在肾脏研究中的前景光明。