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p38α丝裂原活化蛋白激酶对MKK6 mRNA稳定性的负反馈调节

Negative feedback regulation of MKK6 mRNA stability by p38alpha mitogen-activated protein kinase.

作者信息

Ambrosino Concetta, Mace Gaetane, Galban Stefanie, Fritsch Cornelius, Vintersten Kristina, Black Emma, Gorospe Myriam, Nebreda Angel R

机构信息

European Molecular Biology Laboratory, 69117 Heidelberg, Germany.

出版信息

Mol Cell Biol. 2003 Jan;23(1):370-81. doi: 10.1128/MCB.23.1.370-381.2003.

Abstract

p38 mitogen-activated protein (MAP) kinases play an important role in the regulation of cellular responses to all kinds of stresses. The most abundant and broadly expressed p38 MAP kinase is p38alpha, which can also control the proliferation, differentiation, and survival of several cell types. Here we show that the absence of p38alpha correlates with the up-regulation of one of its upstream activators, the MAP kinase kinase MKK6, in p38alpha(-/-) knockout mice and in cultured cells derived from them. In contrast, the expression levels of the p38 activators MKK3 and MKK4 are not affected in p38alpha-deficient cells. The increase in MKK6 protein concentration correlates with increased amounts of MKK6 mRNA in the p38alpha(-/-) cells. Pharmacological inhibition of p38alpha also up-regulates MKK6 mRNA levels in HEK293 cells. Conversely, reintroduction of p38alpha into p38alpha(-/-) cells reduces the levels of MKK6 protein and mRNA to the normal levels found in wild-type cells. Moreover, we show that the MKK6 mRNA is more stable in p38alpha(-/-) cells and that the 3'untranslated region of this mRNA can differentially regulate the stability of the lacZ reporter gene in a p38alpha-dependent manner. Our data indicate that p38alpha can negatively regulate the stability of the MKK6 mRNA and thus control the steady-state concentration of one of its upstream activators.

摘要

p38丝裂原活化蛋白(MAP)激酶在调节细胞对各种应激的反应中起重要作用。最丰富且广泛表达的p38 MAP激酶是p38α,它还可以控制多种细胞类型的增殖、分化和存活。在这里我们表明,在p38α基因敲除小鼠及其衍生的培养细胞中,p38α的缺失与其上游激活剂之一——MAP激酶激酶MKK6的上调相关。相比之下,p38α缺陷细胞中p38的激活剂MKK3和MKK4的表达水平不受影响。p38α(-/-)细胞中MKK6蛋白浓度的增加与MKK6 mRNA量的增加相关。p38α的药理学抑制也上调了HEK293细胞中MKK6 mRNA的水平。相反,将p38α重新导入p38α(-/-)细胞可将MKK6蛋白和mRNA水平降低至野生型细胞中的正常水平。此外,我们表明MKK6 mRNA在p38α(-/-)细胞中更稳定,并且该mRNA的3'非翻译区可以以p38α依赖的方式差异调节lacZ报告基因的稳定性。我们的数据表明,p38α可以负向调节MKK6 mRNA的稳定性,从而控制其上游激活剂之一的稳态浓度。

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