Deshmukh Abhijit S, Agarwal Meetu, Dhar Suman Kumar
National Institute of Animal Biotechnology, Hyderabad, India.
Special Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Curr Genet. 2016 Aug;62(3):481-6. doi: 10.1007/s00294-015-0562-2. Epub 2016 Jan 16.
Regulatory roles of CDKs in fundamental processes including cell cycle progression and transcription are well conserved in metazoans. This family of proteins has undergone significant evolutionary divergence and specialization. Several CDK-like kinases have been identified and characterized in parasitic protozoans. However, clear functional role and physiological relevance of these proteins in protozoans still remain elusive. In continuation with the recent finding that CDK-like protein PfPK5 regulates important DNA replication protein like origin recognition complex subunit 1 in Plasmodium falciparum, here we have discussed the emerging significance of CDK1/2 homologs in DNA replication of parasitic protozoans. In fact, involvement of these proteins in crucial cellular processes projects them as potential drug targets. The possibilities that CDKs offer as potential therapeutic targets in controlling parasite progression have also been explored.
细胞周期蛋白依赖性激酶(CDK)在包括细胞周期进程和转录在内的基本过程中的调控作用在后生动物中得到了很好的保留。这一家族的蛋白质经历了显著的进化分化和特化。在寄生原生动物中已鉴定并表征了几种CDK样激酶。然而,这些蛋白质在原生动物中的明确功能作用和生理相关性仍然难以捉摸。继最近发现CDK样蛋白PfPK5调节恶性疟原虫中重要的DNA复制蛋白如起源识别复合体亚基1之后,我们在此讨论了CDK1/2同源物在寄生原生动物DNA复制中的新意义。事实上,这些蛋白质参与关键细胞过程使其成为潜在的药物靶点。还探讨了CDK作为控制寄生虫进程的潜在治疗靶点的可能性。