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一种门克斯病的小鼠模型揭示了金属硫蛋白的生理功能。

A murine model of Menkes disease reveals a physiological function of metallothionein.

作者信息

Kelly E J, Palmiter R D

机构信息

Department of Biochemistry, University of Washington, Seattle 98195-7370, USA.

出版信息

Nat Genet. 1996 Jun;13(2):219-22. doi: 10.1038/ng0696-219.

Abstract

Human Menkes disease and the murine Mottled phenotype are X-linked diseases that result from copper deficiency due to mutations in a copper-effluxing ATPase, designated ATP7A. Male mice with the Mottled-Brindled allele (Mo-brJ) accumulate copper in the intestine, fail to export copper to peripheral organs and die a few weeks after birth. Much of the intestinal copper is bound by metallothionein (MT). To determine the function of MT in the presence of Atp7a deficiency, we crossed Mo-brJ females with males that bear a targeted disruption of the Mt1 and Mt2 genes (Mt-/-). On an Mt -/- background, most Mo-brJ males as well as heterozygous Mo-brJ females die before embryonic day 11. The lethality in Mo-brJ females can be explained by preferential inactivation of the paternal X chromosome in extraembryonic tissues and resultant copper toxicity in the absence of MT. In support of this hypothesis, cell lines derived from Mt -/-, Mo-brJ embryos are very sensitive to copper toxicity.

摘要

人类门克斯病和小鼠斑驳表型是X连锁疾病,由一种铜转运ATP酶(称为ATP7A)的突变导致铜缺乏引起。具有斑驳-条纹等位基因(Mo-brJ)的雄性小鼠在肠道中积累铜,无法将铜输出到外周器官,并在出生后几周内死亡。大部分肠道铜与金属硫蛋白(MT)结合。为了确定MT在Atp7a缺乏情况下的功能,我们将Mo-brJ雌性与携带Mt1和Mt2基因靶向破坏的雄性(Mt-/-)杂交。在Mt-/-背景下,大多数Mo-brJ雄性以及杂合Mo-brJ雌性在胚胎第11天之前死亡。Mo-brJ雌性的致死性可以通过胚外组织中父本X染色体的优先失活以及在没有MT的情况下产生的铜毒性来解释。支持这一假设的是,源自Mt-/-、Mo-brJ胚胎的细胞系对铜毒性非常敏感。

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