Askari Nadav, Diskin Ron, Avitzour Michal, Capone Ricardo, Livnah Oded, Engelberg David
Department of Biological Chemistry, The Alexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
J Biol Chem. 2007 Jan 5;282(1):91-9. doi: 10.1074/jbc.M608012200. Epub 2006 Nov 6.
The p38 family of kinases is a subgroup of the mitogen-activated protein kinase family. It is composed of four isoforms and is involved in critical biological processes as well as in inflammatory diseases. The exact unique role of each p38 isoform in these processes is not understood well. To approach this question we have been developing intrinsically active variants of p38s. Recently we described a series of mutants of the human p38alpha, which were spontaneously active as recombinant proteins purified from Escherichia coli cells. We show here that some of these mutants are spontaneously active in several mammalian cells in culture. The spontaneous activity of some mutants is higher than the activity of the fully activated wild type counterpart. We further produced mutants of the other p38 isoforms and found that p38beta(D176A), p38gamma(D179A), p38delta(D176A), and p38delta(F324S) are spontaneously active in vivo. The active mutants are also spontaneously phosphorylated. To test whether the mutants actually fulfill downstream duties of p38 proteins, we tested their effect on activating protein 1(AP-1)-mediated transcription. Active mutants of p38alpha induced AP-1-driven reporter genes, as well as the c-jun and c-fos promoters. An active variant of p38gamma suppressed AP-1-mediated transcription. When active variants of p38alpha and p38gamma were co-expressed, AP-1 activity was not induced, showing that p38gamma is dominant over p38alpha with respect to AP-1 activation. Thus, intrinsically active variants that are spontaneously active in vivo have been obtained for all p38 isoforms. These variants have disclosed different effects of each isoform on AP-1 activity.
p38激酶家族是丝裂原活化蛋白激酶家族的一个亚组。它由四种异构体组成,参与关键的生物学过程以及炎症性疾病。每个p38异构体在这些过程中的确切独特作用尚未完全了解。为了解决这个问题,我们一直在开发p38的内在活性变体。最近,我们描述了一系列人类p38α的突变体,它们作为从大肠杆菌细胞中纯化的重组蛋白具有自发活性。我们在此表明,其中一些突变体在培养的几种哺乳动物细胞中具有自发活性。一些突变体的自发活性高于完全活化的野生型对应物的活性。我们进一步产生了其他p38异构体的突变体,发现p38β(D176A)、p38γ(D179A)、p38δ(D176A)和p38δ(F324S)在体内具有自发活性。活性突变体也会自发磷酸化。为了测试这些突变体是否真的履行p38蛋白的下游职责,我们测试了它们对激活蛋白1(AP-1)介导的转录的影响。p38α的活性突变体诱导了AP-1驱动的报告基因以及c-jun和c-fos启动子。p38γ的一个活性变体抑制了AP-1介导的转录。当p38α和p38γ的活性变体共表达时,未诱导AP-1活性,表明在AP-1激活方面p38γ比p38α占优势。因此,已获得了在体内具有自发活性的所有p38异构体的内在活性变体。这些变体揭示了每种异构体对AP-1活性的不同影响。