Evidence that Plasmodium falciparum diacylglycerol acyltransferase is essential for intraerythrocytic proliferation

被引:29
|
作者
Palacpac, NMQ
Hiramine, Y
Seto, S
Hiramatsu, R
Horii, T
Mitamura, T
机构
[1] Japan Sci & Technol Corp, PRESTO, Kawaguchi, Saitama 3320012, Japan
[2] Sumitomo Chem Co Ltd, Takarazuka, Hyogo 6650051, Japan
[3] Osaka Univ, Dept Mol Protozool, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
关键词
malaria; neutral lipid; triacylglycerol; lipid body;
D O I
10.1016/j.bbrc.2004.07.070
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In triacylglycerol (TAG)-accumulating organisms, the physiological roles of diacylglycerol acyltransferase (DGAT), a principal enzyme in the major biosynthetic pathway for TAG, appear to be diverse. Apicomplexan parasite, Plasmodium falciparum, shows unique features in TAG metabolism and trafficking during intraerythrocytic development, and unlike most eukaryotes, only one open reading frame (ORF) encoding a candidate DGAT could be found in its genome. However, whether this candidate ORF encodes P. falciparum DGAT and its physiological relevance have not been assessed. Here, we demonstrate that the ORF is transcribed as a similar to3.6kb single mRNA throughout intraerythrocytic development, markedly elevated at trophozoite, schizont, and segmented schizont, and indeed encodes a protein exhibiting DGAT activity. Further, we provide evidence that the parasite in which the ORF was disrupted via double crossover recombination cannot be enriched, implying a fundamental role of PfDGAT in intraerythrocytic proliferation. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1062 / 1068
页数:7
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