Lenartowicz Małgorzata, Krzeptowski Wojciech
Department of Genetics and Evolution, Institute of Zoology, Jagiellonian University, 6 R. Ingardena St., 30-060 Cracow, Poland.
Postepy Biochem. 2010;56(3):317-27.
Living organisms have developed refined and geneticaly controlled mechanisms of the copper metabolism and transport. ATP7A and ATP7B proteins play the key role in copper homeostasis in the organism. Both proteins are P-type Cu-transporting ATPases and use the energy of ATP hydrolysis to transfer the copper ions across the cellular membranes. Both proteins are localised in Golgi aparatus and involved in regulation of overall copper status in the body and their function is the export of excess copper from the cells and delivery of copper ions to Cu-dependent enzymes. Moreover in organism Cu-transporting ATPases are involved in absorption of dietary copper, Cu removal with the bile, placental copper transport and its secretion to the milk during lactation. Moreover it is known that Cu-transporting ATPases play a role in generation of anti-cancer drug resistance. Disturbances of ATP7A and ATP7B function caused by mutations lead to severe metabolic diseases Menkes and Wilson diseases, respectively.
生物已经进化出了精细且受基因控制的铜代谢和运输机制。ATP7A和ATP7B蛋白在机体铜稳态中起关键作用。这两种蛋白都是P型铜转运ATP酶,利用ATP水解产生的能量将铜离子转运穿过细胞膜。这两种蛋白都定位于高尔基体,参与调节体内整体铜状态,其功能是将多余的铜从细胞中输出,并将铜离子输送到依赖铜的酶中。此外,在生物体内,铜转运ATP酶还参与膳食铜的吸收、胆汁中铜的清除、胎盘铜转运以及哺乳期向乳汁中的铜分泌。此外,已知铜转运ATP酶在抗癌药物耐药性的产生中起作用。由突变引起的ATP7A和ATP7B功能紊乱分别导致严重的代谢性疾病——门克斯病和威尔逊病。