Cragg Ruth A, Christie Graham R, Phillips Siôn R, Russi Rachel M, Küry Sébastien, Mathers John C, Taylor Peter M, Ford Dianne
Department of Biological and Nutritional Sciences, University of Newcastle, Kings Rd., Newcastle upon Tyne, NE1 7RU, United Kingdom.
J Biol Chem. 2002 Jun 21;277(25):22789-97. doi: 10.1074/jbc.M200577200. Epub 2002 Apr 5.
Zinc is essential to a wide range of cellular processes; therefore, it is important to elucidate the molecular mechanisms of zinc homeostasis. To date, no zinc transporters expressed at the enterocyte apical membrane, and so essential to mammalian zinc homeostasis, have been discovered. We identified hZTL1 as a human expressed sequence tag with homology to the basolateral enterocyte zinc transporter ZnT1 and deduced the full-length cDNA sequence by PCR. The protein of 523 amino acids belongs to the cation diffusion facilitator family of membrane transporters. Unusually, the predicted topology comprises 12 rather than 6 transmembrane domains. ZTL1 mRNA was detected by reverse transcription-PCR in a range of mouse tissues. A Myc-tagged hZTL1 clone was expressed in transiently transfected polarized human intestinal Caco-2 cells at the apical membrane. Expression of hZTL1 mRNA in Caco-2 cells increased with zinc supplementation of the nutrient medium; however, in the placental cell line JAR hZTL1 appeared not to be regulated by zinc. Heterologous expression of hZTL1 in Xenopus laevis oocytes increased zinc uptake across the plasma membrane. The localization, regulatory properties, and function of hZTL1 indicate a role in regulating the absorption of dietary zinc across the apical enterocyte membrane.
锌对于广泛的细胞过程至关重要;因此,阐明锌稳态的分子机制很重要。迄今为止,尚未发现有在肠上皮细胞顶端膜表达且对哺乳动物锌稳态至关重要的锌转运蛋白。我们将hZTL1鉴定为与基底外侧肠上皮细胞锌转运蛋白ZnT1具有同源性的人类表达序列标签,并通过PCR推导其全长cDNA序列。该蛋白由523个氨基酸组成,属于膜转运蛋白的阳离子扩散促进剂家族。不同寻常的是,预测的拓扑结构包含12个而非6个跨膜结构域。通过逆转录PCR在一系列小鼠组织中检测到了ZTL1 mRNA。一个带有Myc标签的hZTL1克隆在瞬时转染的极化人肠Caco-2细胞的顶端膜上表达。在营养培养基中添加锌后,Caco-2细胞中hZTL1 mRNA的表达增加;然而,在胎盘细胞系JAR中,hZTL1似乎不受锌的调节。hZTL1在非洲爪蟾卵母细胞中的异源表达增加了跨质膜的锌摄取。hZTL1的定位、调节特性和功能表明其在调节膳食锌通过肠上皮细胞顶端膜的吸收中发挥作用。