首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Drosophila mixed lineage kinase/slipper, a missing biochemical link in Drosophila JNK signaling
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Drosophila mixed lineage kinase/slipper, a missing biochemical link in Drosophila JNK signaling

机译:果蝇混合谱系激酶/拖鞋,果蝇JNK信号中缺少生化联系

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摘要

Mixed lineage kinases (MLKs) belong to the family of mitogen activated protein kinase kinase kinase (MAPKKK) and cause neuronal cell death mediated through c-Jun, N-terminal kinase (JNK) pathway. Recently, genetic studies in Drosophila revealed the presence of an MLK termed slipper (slpr). However, its biochemical features like physiological substrate, role in different MAPK pathways and developmental and tissue-specific expression pattern were not reported. Here, we report cDNA cloning, expression analysis and biochemical characterization of a Drosophila mixed lineage kinase (dMLK) that is also known as slipper. The protein structure analysis of dMLK/slipper revealed, in addition to the conserved domains, a stretch of glutamine in the amino terminus and an asparagine-threonine stretch at the carboxy-terminus. In situ hybridization and reverse transcriptase polymerase chain reaction (RT-PCR) analysis revealed that dMLK is expressed in early embryonic stages, adult brain and thorax. Ectopic expression of dMLK either in Drosophila S2 or in mammalian HEK293 cells leads to activation of JNK, p38 and extracellular signal regulated kinase (ERK) pathways. Further, dMLK directly phosphorylates Hep, dMKK4 and also their mammalian counterparts, MKK7 and SEK1, in an in vitro kinase assay. Taken together, our results provide for the first time a comprehensive expression profile and new biochemical insight of dMLK/slipper.
机译:混合谱系激酶(MLK)属于促分裂原活化蛋白激酶激酶(MAPKKK)家族,可引起通过c-Jun N端激酶(JNK)途径介导的神经元细胞死亡。最近,在果蝇中的遗传研究表明存在称为拖鞋(slpr)的MLK。然而,尚未报道其生化特征,如生理底物,在不同的MAPK途径中的作用以及发育和组织特异性表达模式。在这里,我们报告果蝇混合谱系激酶(dMLK)(也称为拖鞋)的cDNA克隆,表达分析和生化特征。 dMLK /拖鞋的蛋白质结构分析显示,除了保守的结构域外,氨基末端还带有谷氨酰胺,羧基末端带有天冬酰胺-苏氨酸。原位杂交和逆转录聚合酶链反应(RT-PCR)分析表明,dMLK在胚胎早期,成年大脑和胸部表达。果蝇S2或哺乳动物HEK293细胞中dMLK的异位表达导致JNK,p38和细胞外信号调节激酶(ERK)通路的激活。此外,在体外激酶测定中,dMLK将Hep,dMKK4及其哺乳动物对应物MKK7和SEK1直接磷酸化。综上所述,我们的结果首次为dMLK /拖鞋提供了全面的表达概况和新的生化见解。

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