Voss Till S, Kaestli Mirjam, Vogel Denise, Bopp Selina, Beck Hans-Peter
Swiss Tropical Institute, Department of Medical Parasitology and Infection Biology, Socinstrasse 57, 4051 Basel, Switzerland.
Mol Microbiol. 2003 Jun;48(6):1593-607. doi: 10.1046/j.1365-2958.2003.03528.x.
The Plasmodium falciparum virulence factor PfEMP1 is responsible for both antigenic variation and cytoadherence of infected erythrocytes in malaria. Approximately 50 var genes per parasite genome code for this highly polymorphic surface protein. We showed recently that chromosome-central and subtelomeric var genes are controlled by different promoters. Here, we report that transcriptional repression of var genes located in different chromosomal regions occurs by different mechanisms. Subtelomeric var gene transcription is repressed 4-8 h before that of chromosome-central var genes. Both repression events coincide with the shifted expression of two distinct nuclear proteins binding specifically to conserved sequence motifs, SPE1 and CPE, present in the respective promoter. Furthermore, a reiterated and highly conserved subtelomeric var promoter element (SPE2) interacts with a nuclear factor exclusively expressed during S-phase. Promoter analysis by transient transfection suggested direct involvement of these interactions in var gene repression and silencing, and identified regions implicated in transcriptional activation of var genes.
恶性疟原虫的毒力因子恶性疟原虫红细胞膜蛋白1(PfEMP1)负责疟疾感染红细胞的抗原变异和细胞黏附。每个寄生虫基因组大约有50个var基因编码这种高度多态的表面蛋白。我们最近表明,染色体中央和亚端粒var基因由不同的启动子控制。在这里,我们报告位于不同染色体区域的var基因的转录抑制通过不同机制发生。亚端粒var基因转录在染色体中央var基因转录之前4-8小时被抑制。这两种抑制事件都与两种不同的核蛋白的表达变化相吻合,这两种核蛋白特异性结合各自启动子中存在的保守序列基序,即SPE1和CPE。此外,一个重复且高度保守的亚端粒var启动子元件(SPE2)与仅在S期表达的一种核因子相互作用。通过瞬时转染进行的启动子分析表明,这些相互作用直接参与var基因的抑制和沉默,并确定了与var基因转录激活有关的区域。