Adjalley Sophie H, Chabbert Christophe D, Klaus Bernd, Pelechano Vicent, Steinmetz Lars M
Genome Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Genome Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany; Stanford Genome Technology Center, Palo Alto, CA 94304, USA; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cell Rep. 2016 Mar 15;14(10):2463-75. doi: 10.1016/j.celrep.2016.02.025. Epub 2016 Mar 3.
A comprehensive map of transcription start sites (TSSs) across the highly AT-rich genome of P. falciparum would aid progress toward deciphering the molecular mechanisms that underlie the timely regulation of gene expression in this malaria parasite. Using high-throughput sequencing technologies, we generated a comprehensive atlas of transcription initiation events at single-nucleotide resolution during the parasite intra-erythrocytic developmental cycle. This detailed analysis of TSS usage enabled us to define architectural features of plasmodial promoters. We demonstrate that TSS selection and strength are constrained by local nucleotide composition. Furthermore, we provide evidence for coordinate and stage-specific TSS usage from distinct sites within the same transcription unit, thereby producing transcript isoforms, a subset of which are developmentally regulated. This work offers a framework for further investigations into the interactions between genomic sequences and regulatory factors governing the complex transcriptional program of this major human pathogen.
绘制一张覆盖恶性疟原虫高度富含AT基因组的转录起始位点(TSS)综合图谱,将有助于推动对该疟原虫基因表达及时调控背后分子机制的解读。利用高通量测序技术,我们在疟原虫红细胞内发育周期中生成了一张单核苷酸分辨率的转录起始事件综合图谱。对TSS使用情况的详细分析使我们能够定义疟原虫启动子的结构特征。我们证明,TSS的选择和强度受局部核苷酸组成的限制。此外,我们提供了证据,表明同一转录单元内不同位点存在协调且阶段特异性的TSS使用情况,从而产生转录本异构体,其中一部分在发育过程中受到调控。这项工作为进一步研究基因组序列与调控因子之间的相互作用提供了一个框架,这些调控因子控制着这种主要人类病原体复杂的转录程序。