铜
平衡
铜毒性
门克斯病
基因敲除
铜代谢
机制(生物学)
生物
辅因子
化学
细胞生物学
毒性
基因
生物化学
酶
哲学
有机化学
认识论
作者
Alina Fedoseienko,Paulina Bartuzi,Bart van de Sluis
摘要
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.
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