piggyBac is an effective tool for functional analysis of the Plasmodium falciparum genome

被引:58
作者
Balu, Bharath [1 ]
Chauhan, Chitra [1 ]
Maher, Steven P. [1 ]
Shoue, Douglas A. [2 ]
Kissinger, Jessica C. [3 ,4 ]
Fraser, Malcolm J., Jr. [2 ]
Adams, John H. [1 ]
机构
[1] Univ S Florida, Dept Global Hlth, Tampa, FL 33612 USA
[2] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA
[3] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
[4] Univ Georgia, Dept Genet, Athens, GA 30602 USA
来源
BMC MICROBIOLOGY | 2009年 / 9卷
关键词
GENETIC SCREENS; MALARIA; PROTEIN; TRANSFORMATION; EXPRESSION; REVEALS; LIFE; TRANSPOSITION; PHOSPHATASES; MUTAGENESIS;
D O I
10.1186/1471-2180-9-83
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Much of the Plasmodium falciparum genome encodes hypothetical proteins with limited homology to other organisms. A lack of robust tools for genetic manipulation of the parasite limits functional analysis of these hypothetical proteins and other aspects of the Plasmodium genome. Transposon mutagenesis has been used widely to identify gene functions in many organisms and would be extremely valuable for functional analysis of the Plasmodium genome. Results: In this study, we investigated the lepidopteran transposon, piggyBac, as a molecular genetic tool for functional characterization of the Plasmodium falciparum genome. Through multiple transfections, we generated 177 unique P. falciparum mutant clones with mostly single piggyBac insertions in their genomes. Analysis of piggyBac insertion sites revealed random insertions into the P. falciparum genome, in regards to gene expression in parasite life cycle stages and functional categories. We further explored the possibility of forward genetic studies in P. falciparum with a phenotypic screen for attenuated growth, which identified several parasite genes and pathways critical for intra-erythrocytic development. Conclusion: Our results clearly demonstrate that piggyBac is a novel, indispensable tool for forward functional genomics in P. falciparum that will help better understand parasite biology and accelerate drug and vaccine development.
引用
收藏
页数:12
相关论文
共 49 条
[1]   Plasmodium biology:: Genomic gleanings [J].
Aravind, L ;
Iyer, LM ;
Wellems, TE ;
Miller, LH .
CELL, 2003, 115 (07) :771-785
[2]   High-efficiency transformation of Plasmodium falciparum by the lepidopteran transposable element piggyBac [J].
Balu, B ;
Shoue, DA ;
Fraser, MJ ;
Adams, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (45) :16391-16396
[3]   Functional genomics of Plasmodium falciparum through transposon-mediated mutagenesis [J].
Balu, Bharath ;
Adams, John H. .
CELLULAR MICROBIOLOGY, 2006, 8 (10) :1529-1536
[4]   A set of independent selectable markers for transfection of the human malaria parasite Plasmodium falciparum [J].
Ben Mamoun, C ;
Gluzman, IY ;
Goyard, S ;
Beverley, SM ;
Goldberg, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8716-8720
[5]   Maurer's clefts of Plasmodium falciparum are secretory organelles that concentrate virulence protein reporters for delivery to the host erythrocyte [J].
Bhattacharjee, Souvik ;
van Ooij, Christiaan ;
Balu, Bharath ;
Adams, John H. ;
Haldar, Kasturi .
BLOOD, 2008, 111 (04) :2418-2426
[6]   The transcriptome of the intraerythrocytic developmental cycle of Plasmodium falciparum [J].
Bozdech, Z ;
Llinás, M ;
Pulliam, BL ;
Wong, ED ;
Zhu, JC ;
DeRisi, JL .
PLOS BIOLOGY, 2003, 1 (01) :85-100
[7]   Somatic integration of an oncogene-harboring Sleeping Beauty transposon models liver tumor development in the mouse [J].
Carlson, CM ;
Frandsen, JL ;
Kirchhof, N ;
McIvor, RS ;
Largaespada, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (47) :17059-17064
[8]   TRANSPOSON MUTAGENESIS OF BACULOVIRUSES - ANALYSIS OF TRICHOPLUSIA-NI TRANSPOSON IFP2 INSERTIONS WITHIN THE FP-LOCUS OF NUCLEAR POLYHEDROSIS VIRUSES [J].
CARY, LC ;
GOEBEL, M ;
CORSARO, BG ;
WANG, HG ;
ROSEN, E ;
FRASER, MJ .
VIROLOGY, 1989, 172 (01) :156-169
[9]   Global control of gene expression in yeast by the Ccr4-Not complex [J].
Collart, MA .
GENE, 2003, 313 :1-16
[10]   Comparative genomics of transcriptional control in the human malaria parasite Plasmodium falciparum [J].
Coulson, RMR ;
Hall, N ;
Ouzounis, CA .
GENOME RESEARCH, 2004, 14 (08) :1548-1554