Literature DB >> 20870716

PfSRPK1, a novel splicing-related kinase from Plasmodium falciparum.

Aparna Dixit1, Prashant K Singh, Guru Prasad Sharma, Pawan Malhotra, Pushkar Sharma.   

Abstract

Even though it is increasingly evident that post-transcriptional events like mRNA processing and splicing may regulate gene expression and proteome diversity of malaria parasite Plasmodium, molecular mechanisms that regulate events like mRNA splicing in malaria parasite are poorly understood. Protein kinases control a wide variety of cellular events in almost all eukaryotes, including modulation of mRNA splicing, transport, and stability. We have identified a novel splicing-related protein kinase from Plasmodium falciparum, PfSRPK1. PfSRPK1 when incubated with parasite nuclear extracts inhibited RNA splicing, suggesting that it may control mRNA splicing in the parasite. PfSR1, a putative splicing factor from P. falciparum, was identified as a substrate of PfSRPK1. PfSR1 interacts with RNA and PfSRPK1 modulates its RNA binding. Early in the parasite development, PfSRPK1 and PfSR1 are present in the nucleus. These studies provide useful insights into the function of two potentially key components of P. falciparum mRNA splicing machinery.

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Year:  2010        PMID: 20870716      PMCID: PMC2992265          DOI: 10.1074/jbc.M110.119255

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  40 in total

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Journal:  J Biol Chem       Date:  2003-03-31       Impact factor: 5.157

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9.  PfPKB, a novel protein kinase B-like enzyme from Plasmodium falciparum: I. Identification, characterization, and possible role in parasite development.

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  16 in total

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2.  Global analysis of protein expression and phosphorylation of three stages of Plasmodium falciparum intraerythrocytic development.

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Review 4.  Enzyme Activity Assays for Protein Kinases: Strategies to Identify Active Substrates.

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7.  A novel Plasmodium falciparum SR protein is an alternative splicing factor required for the parasites' proliferation in human erythrocytes.

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8.  Changes in the transcriptome of the malaria parasite Plasmodium falciparum during the initial phase of transmission from the human to the mosquito.

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10.  A novel subnetwork alignment approach predicts new components of the cell cycle regulatory apparatus in Plasmodium falciparum.

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