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X连锁低磷血症:人类和小鼠中的一种同源性疾病。

X-linked hypophosphataemia: a homologous disorder in humans and mice.

作者信息

Tenenhouse H S

机构信息

Department of Pediatrics, McGill University, Montreal Children's Hospital Research Institute, Quebec, Canada.

出版信息

Nephrol Dial Transplant. 1999 Feb;14(2):333-41. doi: 10.1093/ndt/14.2.333.

Abstract

X-linked hypophosphatemia is an inherited disorder of phosphate (Pi) homeostasis characterized by growth retardation, rickets and osteomalacia, hypophosphataemia, and aberrant renal Pi reabsorption and vitamin D metabolism. Studies in murine Hyp and Gy homologues have identified a specific defect in Na+-Pi cotransport at the brush border membrane, abnormal regulation of 1,25-dihydroxyvitamin D3 (1,25(OH)2D) synthesis and degradation, and an intrinsic defect in bone mineralization. The mutant gene has been identified in XLH patients, by positional cloning, and in Hyp and Gy mice, and was designated PHEX/Phex to signify a PHosphate-regulating gene with homology to Endopeptidases on the X chromosome. PHEX/Phex is expressed in bones and teeth but not in kidney and efforts are under way to elucidate how loss of PHEX/Phex function elicits the mutant phenotype. Based on its homology to endopeptidases, it is postulated that PHEX/Phex is involved in the activation or inactivation of a peptide hormone(s) which plays a key role in the regulation of bone mineralization, renal Pi handling and vitamin D metabolism.

摘要

X连锁低磷血症是一种遗传性磷(Pi)稳态紊乱疾病,其特征为生长发育迟缓、佝偻病和骨软化症、低磷血症以及异常的肾脏Pi重吸收和维生素D代谢。对小鼠Hyp和Gy同源物的研究已确定在刷状缘膜上Na+-Pi共转运存在特定缺陷、1,25-二羟维生素D3(1,25(OH)2D)合成与降解的调节异常以及骨矿化存在内在缺陷。通过定位克隆在XLH患者以及Hyp和Gy小鼠中鉴定出了突变基因,该基因被命名为PHEX/Phex,以表示与X染色体上内肽酶具有同源性的磷酸盐调节基因。PHEX/Phex在骨骼和牙齿中表达,但在肾脏中不表达,目前正在努力阐明PHEX/Phex功能丧失如何引发突变表型。基于其与内肽酶的同源性,推测PHEX/Phex参与了一种肽激素的激活或失活,该肽激素在骨矿化、肾脏Pi处理和维生素D代谢的调节中起关键作用。

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