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Human mitogen-activated protein kinase kinase kinase mediates the stress-induced activation of mitogen-activated protein kinase cascades.

机译:人促分裂原激活的蛋白激酶激酶激酶介导应激诱导的促分裂原激活的蛋白激酶级联反应。

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摘要

The mitogen-activated protein kinase (MAPK) cascades represent one of the important signalling mechanisms in response to environmental stimuli. We report the identification of a human MAPK kinase kinase, MAPKKK4, via sequence similarity with other MAPKKKs. When truncated MAPKKK4 (DeltaMAPKKK4) was overexpressed in HEK293 cells, it was constitutively active and induced the activation of endogenous p38alpha, c-Jun N-terminal kinase (JNK)1/2 and extracellular signal-regulated kinase (ERK)2 in vivo. Kinase-inactive DeltaMAPKKK4 partly inhibited the activation of p38alpha, JNK1/2 and ERK2 induced by stress, tumour necrosis factor alpha or epidermal growth factor, suggesting that MAPKKK4 might be physiologically involved in all three MAPK cascades. Co-expressed MAP kinase kinase (MKK)-1, MKK-4, MKK-3 and MKK-6 were activated in vivo by DeltaMAPKKK4. All of the above MKKs purified from Escherichia coli were phosphorylated and activated by DeltaMAPKKK4 immunoprecipitates in vitro. When expressed by lower plasmid doses, DeltaMAPKKK4 preferentially activated MKK-3 and p38alpha in vivo. Overexpression of DeltaMAPKKK4 did not activate the NF-kappaB pathway. Immunoprecipitation of endogenous MAPKKK4 by specific antibodies showed that MAPKKK4 was activated after the treatment of K562 cells with various stress conditions. As a broadly distributed kinase, MAPKKK4 might serve as a stress responder. MAPKKK4 is 91% identical with the recently described murine MEKK-4beta and might be its human homologue. It is also identical with the recently cloned human MAP three kinase 1 except for the lack of an internal sequence homologous to the murine MEKK-4alpha isoform. Differences in the reported functional activities of the three kinases are discussed.
机译:有丝分裂原激活的蛋白激酶(MAPK)级联代表了对环境刺激作出反应的重要信号传导机制之一。我们报告通过与其他MAPKKKs的序列相似性鉴定人类MAPK激酶激酶MAPKKK4。当截短的MAPKKK4(DeltaMAPKKK4)在HEK293细胞中过表达时,它具有组成型活性,并在体内诱导内源性p38alpha,c-Jun N端激酶(JNK)1/2和细胞外信号调节激酶(ERK)2的激活。激酶失活的DeltaMAPKKK4部分抑制了由应激,肿瘤坏死因子α或表皮生长因子诱导的p38alpha,JNK1 / 2和ERK2的激活,这表明MAPKKK4可能在所有三个MAPK级联中均涉及生理。共表达的MAP激酶激酶(MKK)-1,MKK-4,MKK-3和MKK-6在体内被DeltaMAPKKK4激活。从大肠杆菌中纯化的所有上述MKK均在体外被DeltaMAPKKK4免疫沉淀磷酸化并激活。当以较低的质粒剂量表达时,DeltaMAPKKK4在体内优先激活MKK-3和p38alpha。 DeltaMAPKKK4的过表达不会激活NF-κB途径。通过特异性抗体对内源性MAPKKK4的免疫沉淀表明,在各种胁迫条件下处理K562细胞后,MAPKKK4被激活。作为广泛分布的激酶,MAPKKK4可以作为应激反应者。 MAPKKK4与最近描述的鼠MEKK-4beta 91%相同,可能是其人类同源物。除了缺乏与鼠MEKK-4α同工型同源的内部序列外,它还与最近克隆的人MAP 3激酶1相同。讨论了三种激酶报道的功能活性的差异。

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    Chan-Hui, P Y; Weaver, R;

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  • 年度 1998
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  • 正文语种 en
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