A novel zinc-regulated human zinc transporter, hZTL1, is localized to the enterocyte apical membrane

被引:114
作者
Cragg, RA
Christie, GR
Phillips, SR
Russi, RM
Küry, S
Mathers, JC
Taylor, PM
Ford, D
机构
[1] Univ Newcastle, Dept Biol & Nutr Sci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Newcastle, Human Nutr Res Ctr, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Univ Dundee, Sch Life Sci, Div Mol Physiol, Dundee DD1 5EH, Scotland
[4] Fac Med, ADN, Lab Etud Polymorphisme, F-44035 Nantes, France
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1074/jbc.M200577200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:22789 / 22797
页数:9
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