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小鼠ank基因在组织钙化和关节炎控制中的作用。

Role of the mouse ank gene in control of tissue calcification and arthritis.

作者信息

Ho A M, Johnson M D, Kingsley D M

机构信息

Department of Developmental Biology and Howard Hughes Medical Institute, Beckman Center B300, Stanford University School of Medicine, Stanford, CA 94305-5327, USA.

出版信息

Science. 2000 Jul 14;289(5477):265-70. doi: 10.1126/science.289.5477.265.

Abstract

Mutation at the mouse progressive ankylosis (ank) locus causes a generalized, progressive form of arthritis accompanied by mineral deposition, formation of bony outgrowths, and joint destruction. Here, we show that the ank locus encodes a multipass transmembrane protein (ANK) that is expressed in joints and other tissues and controls pyrophosphate levels in cultured cells. A highly conserved gene is present in humans and other vertebrates. These results identify ANK-mediated control of pyrophosphate levels as a possible mechanism regulating tissue calcification and susceptibility to arthritis in higher animals.

摘要

小鼠进行性关节强硬(ank)位点的突变会引发一种全身性、进行性的关节炎,伴有矿物质沉积、骨赘形成和关节破坏。在此,我们表明ank位点编码一种多次跨膜蛋白(ANK),该蛋白在关节和其他组织中表达,并控制培养细胞中的焦磷酸水平。人类和其他脊椎动物中存在一个高度保守的基因。这些结果表明,ANK介导的焦磷酸水平控制可能是调节高等动物组织钙化和关节炎易感性的一种机制。

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