Regulatory motifs uncovered among gene expression clusters in Plasmodium falciparum

被引:27
作者
Gunasekera, Anusha M.
Myrick, Alissa
Militello, Kevin T.
Sims, Jennifer S.
Dong, Carolyn K.
Gierahn, Todd
Le Roch, Karine
Winzeler, Elizabeth
Wirth, Dyann F. [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infrct Dis, Boston, MA 02115 USA
[2] Scripps Res Inst, La Jolla, CA USA
基金
英国惠康基金;
关键词
gene regulation; Plasmodium falciparum; oligonucleotide array; regulatory motifs;
D O I
10.1016/j.molbiopara.2007.01.011
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
Control of gene expression is poorly understood in the Plasmodium system, where relatively few homologues to known eukaryotic transcription factors have been uncovered. Recent evidence suggests that the parasite may utilize a combinatorial mode of gene regulation, with multiple cis-acting sequences contributing to overall activity at individual promoters [1]. To further probe this mechanism of control, we,first searched for over-represented sequence motifs among gene clusters sharing similar expression profiles in Plasmodium falciparum. More specifically, we applied bioinformatic tools to a previously characterized micro-array data set from drug-treated asexual stage cultures (Gunasekera et al., submitted). Cluster analysis of 600 drug responsive genes identified only a single 5' motif, GAGAGAA. Two additional 5' motifs, ACTATAAAGA and TGCAC, were also shared among loci displaying patterns of coordinate expression across varying asexual growth stages. Secondly and most importantly, the functional relevance of each motif was tested in two independent assays-transient transfection and gel-retardation experiments. The GAGAGAA and TGCAC motifs were both active in the former. The GAGAGAA and ACTATAAAGA elements formed specific RNA-protein, but not DNA-protein complexes in gel shift assays, suggesting a key level of control at the RNA level. This is the first report of functionally characterized motifs in P. falciparum that were uncovered following clustering analysis of its asexual stage transcriptome. Together, both the bioinformatic and functional data reported here imply that multiple forms of gene regulation, including post-transcriptional control, may be important in the malarial system. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 30
页数:12
相关论文
共 57 条
[31]   New insights into the pleiotropic drug resistance network from genome-wide characterization of the YRR1 transcription factor regulation system [J].
Le Crom, S ;
Devaux, F ;
Marc, P ;
Zhang, XT ;
Moye-Rowley, WS ;
Jacq, C .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (08) :2642-2649
[32]   Global analysis of transcript and protein levels across the Plasmodium falciparum life cycle [J].
Le Roch, KG ;
Johnson, JR ;
Florens, L ;
Zhou, YY ;
Santrosyan, A ;
Grainger, M ;
Yan, SF ;
Williamson, KC ;
Holder, AA ;
Carucci, DJ ;
Yates, JR ;
Winzeler, EA .
GENOME RESEARCH, 2004, 14 (11) :2308-2318
[33]   Discovery of gene function by expression profiling of the malaria parasite life cycle [J].
Le Roch, KG ;
Zhou, YY ;
Blair, PL ;
Grainger, M ;
Moch, JK ;
Haynes, JD ;
De la Vega, P ;
Holder, AA ;
Batalov, S ;
Carucci, DJ ;
Winzeler, EA .
SCIENCE, 2003, 301 (5639) :1503-1508
[34]   Expression of a recombinant IRP-like Plasmodium falciparum protein that specifically binds putative plasmodial IREs [J].
Loyevsky, M ;
Mompoint, F ;
Yikilmaz, E ;
Altschul, SF ;
Madden, T ;
Wootton, JC ;
Kurantsin-Mills, J ;
Kassim, OO ;
Gordeuk, VR ;
Rouault, TA .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2003, 126 (02) :231-238
[35]   An IRP-like protein from Plasmodium falciparum binds to a mammalian iron-responsive element [J].
Loyevsky, M ;
LaVaute, T ;
Allerson, CR ;
Stearman, R ;
Kassim, OO ;
Cooperman, S ;
Gordeuk, VR ;
Rouault, TA .
BLOOD, 2001, 98 (08) :2555-2562
[36]   Early expression of yeast genes affected by chemical stress [J].
Lucau-Danila, A ;
Lelandais, G ;
Kozovska, Z ;
Tanty, V ;
Delaveau, T ;
Devaux, F ;
Jacq, C .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (05) :1860-1868
[37]   Regulation of sexual development of Plasmodium by translational repression [J].
Mair, Gunnar R. ;
Braks, Joanna A. M. ;
Garver, Lindsey S. ;
Wiegant, Loop C. A. G. ;
Hall, Neil ;
Dirks, Roeland W. ;
Khan, Shahid M. ;
Dimopoulos, George ;
Janse, Chris J. ;
Waters, Andrew P. .
SCIENCE, 2006, 313 (5787) :667-669
[38]   Transcription of Leishmania major Friedlin chromosome 1 initiates in both directions within a single region [J].
Martínez-Calvillo, S ;
Yan, SF ;
Nguyen, D ;
Fox, M ;
Stuart, K ;
Myler, PJ .
MOLECULAR CELL, 2003, 11 (05) :1291-1299
[39]   VISTA:: visualizing global DNA sequence alignments of arbitrary length [J].
Mayor, C ;
Brudno, M ;
Schwartz, JR ;
Poliakov, A ;
Rubin, EM ;
Frazer, KA ;
Pachter, LS ;
Dubchak, I .
BIOINFORMATICS, 2000, 16 (11) :1046-1047
[40]   Deletion analysis of the 5′ flanking sequence of the Plasmodium gallinaceum sexual stage specific gene pgs28 suggests a bipartite arrangement of cis-control elements [J].
Mbacham, WF ;
Chow, CS ;
Daily, J ;
Golightly, LM ;
Wirth, DF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 113 (01) :183-187