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糖原贮积病Ib型中发生突变的假定葡萄糖6-磷酸转运体的序列。

Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib.

作者信息

Gerin I, Veiga-da-Cunha M, Achouri Y, Collet J F, Van Schaftingen E

机构信息

Laboratory of Physiological Chemistry, Institute of Cellular Pathology and University of Louvain, Brussels, Belgium.

出版信息

FEBS Lett. 1997 Dec 15;419(2-3):235-8. doi: 10.1016/s0014-5793(97)01463-4.

Abstract

We report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologous to bacterial transporters for phosphate esters. This protein presents at its carboxy terminus the consensus motif for retention in the endoplasmic reticulum. Northern blots of rat tissues indicate that the corresponding mRNA is mostly expressed in liver and kidney. In two patients with glycogen storage disease type Ib, mutations were observed that either replaced a conserved Gly to Cys or introduced a premature stop codon. The encoded protein is therefore most likely the glucose 6-phosphate translocase that is functionally associated with glucose-6-phosphatase.

摘要

我们报道了一种人类cDNA的序列,该序列编码一种46 kDa的跨膜蛋白,与细菌磷酸酯转运蛋白同源。这种蛋白在其羧基末端呈现出在内质网中保留的共有基序。大鼠组织的Northern印迹表明,相应的mRNA主要在肝脏和肾脏中表达。在两名I b型糖原贮积病患者中,观察到了突变,这些突变要么将保守的甘氨酸替换为半胱氨酸,要么引入了提前终止密码子。因此,所编码的蛋白很可能是与葡萄糖-6-磷酸酶功能相关的葡萄糖6-磷酸转运体。

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