Lye Yu Min, Chan Maurice, Sim Tiow-Suan
Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, MD4A, 5 Science Drive 2, Singapore 117597, Republic of Singapore.
FEBS Lett. 2006 Nov 13;580(26):6083-92. doi: 10.1016/j.febslet.2006.10.003. Epub 2006 Oct 12.
The canonical mitogen-activated protein kinase (MAPK) signal cascade was previously suggested to be atypical in the malaria parasite. This raises queries on the existence of alternative mediators of plasmodial MAPK pathways. This study describes, Pfnek3, a malarial protein kinase belonging to the NIMA (Never in Mitosis, Aspergillus) family. Endogenous Pfnek3 is expressed during late asexual to gametocyte stages and lacks some classical protein kinase sequence motifs. Moreover, Pfnek3 is phylogenetically distant from mammalian NIMA-kinases. Recombinant Pfnek3 was able to phosphorylate and stimulate a malarial MAPK (Pfmap2). Contrastingly, this was not observed with two other kinases, Pfmap1 and human MAPK1, suggesting that the Pfnek3-Pfmap2 interaction may be specific for Pfmap2 regulation. In summary, our data reveal a malarial NIMA-kinase with the potential to regulate a MAPK. Possessing biochemical properties divergent from classical mammalian NIMA-kinases, Pfnek3 could potentially be an attractive target for parasite-selective anti-malarials.
经典的丝裂原活化蛋白激酶(MAPK)信号级联先前被认为在疟原虫中是非典型的。这引发了关于疟原虫MAPK途径替代介质存在的疑问。本研究描述了Pfnek3,一种属于NIMA(有丝分裂中从不,曲霉属)家族的疟疾蛋白激酶。内源性Pfnek3在无性后期到配子体阶段表达,并且缺乏一些经典的蛋白激酶序列基序。此外,Pfnek3在系统发育上与哺乳动物NIMA激酶相距甚远。重组Pfnek3能够磷酸化并刺激疟疾MAPK(Pfmap2)。相反,在另外两种激酶Pfmap1和人类MAPK1中未观察到这种情况,这表明Pfnek3-Pfmap2相互作用可能对Pfmap2调节具有特异性。总之,我们的数据揭示了一种具有调节MAPK潜力的疟疾NIMA激酶。Pfnek3具有与经典哺乳动物NIMA激酶不同的生化特性,可能是寄生虫选择性抗疟药物的一个有吸引力的靶点。