University of Groningen, University Medical Center Groningen, Molecular Genetics section, Groningen, the Netherlands.
Ann N Y Acad Sci. 2014 May;1314:6-14. doi: 10.1111/nyas.12353. Epub 2014 Feb 12.
Copper is an important cofactor in numerous biological processes in all living organisms. However, excessive copper can be extremely toxic, so it is vital that the copper level within a cell is tightly regulated. The damaging effect of copper is seen in several hereditary forms of copper toxicity in humans and animals. At present, Wilson's disease is the best-described and best-studied copper-storage disorder in humans; it is caused by mutations in the ATP7B gene. In dogs, a mutation in the COMMD1 gene has been found to be associated with copper toxicosis. Using a liver-specific Commd1 knockout mouse, the biological role of Commd1 in copper homeostasis has been confirmed. Yet, the exact mechanism by which COMMD1 regulates copper homeostasis is still unknown. Here, we give an overview of the current knowledge and perspectives on the molecular function of COMMD1 in copper homeostasis.
铜是所有生物体中许多生物过程的重要辅助因子。然而,过量的铜可能是极其有毒的,因此细胞内的铜含量必须得到严格控制。在人类和动物的几种遗传性铜毒性形式中可以看到铜的破坏作用。目前,Wilson 病是人类描述和研究得最好的铜储存障碍;它是由 ATP7B 基因突变引起的。在狗中,已经发现 COMMD1 基因的突变与铜中毒有关。使用肝脏特异性 Commd1 敲除小鼠,证实了 Commd1 在铜动态平衡中的生物学作用。然而,COMMD1 调节铜动态平衡的确切机制尚不清楚。在这里,我们概述了 COMMD1 在铜动态平衡中的分子功能的最新知识和观点。