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阳离子扩散促进因子基因 cdf-2 介导秀丽隐杆线虫的锌代谢。

The cation diffusion facilitator gene cdf-2 mediates zinc metabolism in Caenorhabditis elegans.

机构信息

Department of Developmental Biology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.

出版信息

Genetics. 2009 Aug;182(4):1015-33. doi: 10.1534/genetics.109.103614. Epub 2009 May 17.

Abstract

Zinc is essential for many cellular processes. To use Caenorhabditis elegans to study zinc metabolism, we developed culture conditions allowing full control of dietary zinc and methods to measure zinc content of animals. Dietary zinc dramatically affected growth and zinc content; wild-type worms survived from 7 microm to 1.3 mm dietary zinc, and zinc content varied 27-fold. We investigated cdf-2, which encodes a predicted zinc transporter in the cation diffusion facilitator family. cdf-2 mRNA levels were increased by high dietary zinc, suggesting cdf-2 promotes zinc homeostasis. CDF-2 protein was expressed in intestinal cells and localized to cytosolic vesicles. A cdf-2 loss-of-function mutant displayed impaired growth and reduced zinc content, indicating that CDF-2 stores zinc by transport into the lumen of vesicles. The relationships between three cdf genes, cdf-1, cdf-2, and sur-7, were analyzed in double and triple mutant animals. A cdf-1 mutant displayed increased zinc content, whereas a cdf-1 cdf-2 double mutant had intermediate zinc content, suggesting cdf-1 and cdf-2 have antagonistic functions. These studies advance C. elegans as a model of zinc metabolism and identify cdf-2 as a new gene that has a critical role in zinc storage.

摘要

锌是许多细胞过程所必需的。为了使用秀丽隐杆线虫来研究锌代谢,我们开发了允许完全控制饮食中锌的条件和测量动物锌含量的方法。饮食中的锌对生长和锌含量有显著影响;野生型线虫可以在 7 微米至 1.3 毫米的饮食锌浓度下存活,锌含量变化了 27 倍。我们研究了 cdf-2,它编码阳离子扩散促进因子家族中的一种预测锌转运体。高饮食锌增加了 cdf-2 的 mRNA 水平,表明 cdf-2 促进锌的稳态。CDF-2 蛋白在肠细胞中表达,并定位于细胞质小泡。cdf-2 功能丧失突变体的生长受损且锌含量降低,表明 CDF-2 通过转运到小泡腔来储存锌。在双突变和三突变动物中分析了三个 cdf 基因 cdf-1、cdf-2 和 sur-7 之间的关系。cdf-1 突变体的锌含量增加,而 cdf-1 cdf-2 双突变体的锌含量居中,表明 cdf-1 和 cdf-2 具有拮抗作用。这些研究推进了秀丽隐杆线虫作为锌代谢模型,并确定了 cdf-2 作为一个在锌储存中具有关键作用的新基因。

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