Dufner-Beattie Jodi, Wang Fudi, Kuo Yien-Ming, Gitschier Jane, Eide David, Andrews Glen K
Department of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City, Kansas 66160-7421, USA.
J Biol Chem. 2003 Aug 29;278(35):33474-81. doi: 10.1074/jbc.M305000200. Epub 2003 Jun 11.
The human ZIP4 gene (SLC39A4) is a candidate for the genetic disorder of zinc metabolism acrodermatitis enteropathica. To understand its role in zinc homeostasis, we examined the function and expression of mouse ZIP4. This gene encodes a well conserved eight-transmembrane protein that can specifically increase the influx of zinc into transfected cells. Expression of this gene is robust in tissues involved in nutrient uptake, such as the intestines and embryonic visceral yolk sac, and is dynamically regulated by zinc. Dietary zinc deficiency causes a marked increase in the accumulation of ZIP4 mRNA in these tissues, whereas injection of zinc or increasing zinc content of the diet rapidly reduces its abundance. Zinc can also regulate the accumulation of ZIP4 protein at the apical surface of enterocytes and visceral endoderm cells. These results provide compelling evidence that ZIP4 is a zinc transporter that plays an important role in zinc homeostasis, a process that is defective in acrodermatitis enteropathica in humans.
人类ZIP4基因(SLC39A4)是锌代谢紊乱疾病肠病性肢端皮炎的一个候选基因。为了解其在锌稳态中的作用,我们研究了小鼠ZIP4的功能和表达。该基因编码一种高度保守的八次跨膜蛋白,它能够特异性地增加锌流入转染细胞的量。该基因在参与营养物质吸收的组织中,如肠道和胚胎内脏卵黄囊中表达强烈,并且受锌的动态调节。饮食中锌缺乏会导致这些组织中ZIP4 mRNA的积累显著增加,而注射锌或增加饮食中的锌含量会迅速降低其丰度。锌还可以调节ZIP4蛋白在肠上皮细胞和内脏内胚层细胞顶端表面的积累。这些结果提供了令人信服的证据,表明ZIP4是一种锌转运蛋白,在锌稳态中起重要作用,而在人类肠病性肢端皮炎中该过程存在缺陷。