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编码人破骨细胞特异性116-kDa V-ATP酶亚基小鼠同源物的基因在骨硬化(oc/oc)突变体中存在缺失。

The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants.

作者信息

Scimeca J C, Franchi A, Trojani C, Parrinello H, Grosgeorge J, Robert C, Jaillon O, Poirier C, Gaudray P, Carle G F

机构信息

Instabilité et Altérations des Génomes, UMR6549 CNRS/UNSA, Faculté de Médecine de l'Université de Nice-Sophia Antipolis, Nice, France.

出版信息

Bone. 2000 Mar;26(3):207-13. doi: 10.1016/s8756-3282(99)00278-1.

Abstract

Osteosclerosis (oc) is an autosomal recessive lethal mutation that impairs bone resorption by osteoclasts, and induces a general increase of bone density in affected mice. Genetic mapping of the oc mutation was used as a backbone in a positional cloning approach in the pericentromeric region of mouse chromosome 19. Perfect cosegregation of the osteopetrotic phenotype with polymorphic markers enabled the construction of a sequence-ready bacterial artificial chromosome (BAC) contig of this region. Genomic sequencing of a 200-kb area revealed the presence of the mouse homologue to the human gene encoding the osteoclast-specific 116-kDa subunit of the vacuolar proton pump. This gene was located recently on human 11q13, a genomic region conserved with proximal mouse chromosome 19. Sequencing of the 5' end of the gene in oc/oc mice showed a 1.6-kb deletion, including the translation start site, which impairs genuine transcription of this subunit. The inactivation of this osteoclast-specific vacuolar proton ATPase subunit could be responsible for the lack of this enzyme in the apical membranes of osteoclast cells in oc/oc mice, thereby preventing the resorption function of these cells, which leads to the osteopetrotic phenotype.

摘要

骨硬化症(oc)是一种常染色体隐性致死突变,它会损害破骨细胞的骨吸收功能,并导致受影响小鼠的骨密度普遍增加。oc突变的基因定位被用作在小鼠19号染色体着丝粒周围区域进行定位克隆的基础。骨石化表型与多态性标记的完美共分离使得能够构建该区域的序列就绪细菌人工染色体(BAC)重叠群。对一个200kb区域的基因组测序揭示了与编码液泡质子泵破骨细胞特异性116kDa亚基的人类基因的小鼠同源物的存在。该基因最近定位在人类11q13上,这是一个与小鼠近端19号染色体保守的基因组区域。对oc/oc小鼠中该基因5'端的测序显示有一个1.6kb的缺失,包括翻译起始位点,这损害了该亚基的正常转录。这种破骨细胞特异性液泡质子ATP酶亚基的失活可能是oc/oc小鼠破骨细胞顶端膜中缺乏这种酶的原因,从而阻止了这些细胞的吸收功能,导致骨石化表型。

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