Polysome profiling of the malaria parasite Plasmodium falciparum

被引:24
作者
Lacsina, Joshua R.
LaMonte, Gregory [2 ]
Nicchitta, Christopher V. [1 ]
Chi, Jen-Tsan [2 ]
机构
[1] Duke Univ, Med Ctr, Sch Med, Dept Pathol, Durham, NC 27710 USA
[2] Duke Univ, Sch Med, Inst Genome Sci & Policy, Durham, NC 27710 USA
关键词
Malaria; Plasmodium falciparum; Polysome; Translation; Post-transcriptional regulation; Global; IN-VITRO; RNA; LIFE; TRANSLATION;
D O I
10.1016/j.molbiopara.2011.05.003
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 the malaria parasite Plasmodium falciparum, global studies of translational regulation have been hampered by the inability to isolate malaria polysomes. We describe here a novel method for polysome profiling in P. falciparum, a powerful approach which allows both a global view of translation and the measurement of ribosomal loading and density for specific mRNAs. Simultaneous lysis of infected erythrocytes and parasites releases stable, intact malaria polysomes, which are then purified by centrifugation through a sucrose cushion. The polysomes are resuspended, separated by velocity sedimentation and then fractionated, yielding a characteristic polysome profile reflecting the global level of translational activity in the parasite. RNA isolated from specific fractions can be used to determine the density of ribosomes loaded onto a particular transcript of interest, and is free of host ribosome contamination. Thus, our approach opens translational regulation in malaria to genome-wide analysis. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 46
页数:5
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