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法呢基焦磷酸激酶缺乏导致 RhoA 和 Rac1 的 geranylgeranylation 受损。

Compromized geranylgeranylation of RhoA and Rac1 in mevalonate kinase deficiency.

机构信息

Department of Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

J Inherit Metab Dis. 2010 Oct;33(5):625-32. doi: 10.1007/s10545-010-9173-8. Epub 2010 Sep 3.

Abstract

Mevalonate kinase deficiency (MKD) is an autoinflammatory disorder caused by mutations in the MVK gene resulting in decreased activity of the enzyme mevalonate kinase (MK). Although MK is required for biosynthesis of all isoprenoids, in MKD, in particular, the timely synthesis of geranylgeranyl pyrophosphate appears to be compromised. Because small guanosine triphosphatases (GTPases) depend on geranylgeranylation for their proper signaling function, we studied the effect of MK deficiency on geranylgeranylation and activation of the two small GTPases, RhoA and Rac1. We demonstrate that both geranylgeranylation and activation of the two GTPases are more easily disturbed in MKD cells than in control cells when the flux though the isoprenoid biosynthesis pathway is suppressed by low concentrations of simvastatin. The limited capacity of geranylgeranylation in MKD cells readily leads to markedly increased levels of nonisoprenylated and activated GTPases, which will affect proper signaling by these GTPases.

摘要

甲羟戊酸激酶缺乏症(MKD)是一种由 MVK 基因突变引起的自身炎症性疾病,导致甲羟戊酸激酶(MK)活性降低。尽管 MK 是所有异戊烯基化合物生物合成所必需的,但在 MKD 中,特别是法尼基焦磷酸(geranylgeranyl pyrophosphate)的及时合成似乎受到了影响。由于小分子鸟苷三磷酸酶(GTPases)依赖于 geranylgeranylation 来发挥其适当的信号功能,我们研究了 MK 缺乏对两种小分子 GTPases RhoA 和 Rac1 的 geranylgeranylation 和激活的影响。我们证明,当异戊烯基生物合成途径的通量被低浓度辛伐他汀抑制时,MKD 细胞中的两种 GTPases 的 geranylgeranylation 和激活比对照细胞更容易受到干扰。MKD 细胞中 geranylgeranylation 的有限能力很容易导致非异戊烯基化和激活的 GTPases 水平显著增加,这将影响这些 GTPases 的适当信号转导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf7a/2946549/eb72157ce5a0/10545_2010_9173_Fig1_HTML.jpg

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