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疟原虫的基因组学和综合系统生物学:通往疟疾控制和消除的道路。

Genomics and integrated systems biology in Plasmodium falciparum: a path to malaria control and eradication.

机构信息

Department of Cell Biology and Neuroscience, University of California Riverside, Institute for Integrative Genome Biology, and Center for Disease Vector Research, Riverside, CA 92521, USA.

出版信息

Parasite Immunol. 2012 Feb-Mar;34(2-3):50-60. doi: 10.1111/j.1365-3024.2011.01340.x.

DOI:10.1111/j.1365-3024.2011.01340.x
PMID:21995286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3265687/
Abstract

The first draft of the human malaria parasite's genome was released in 2002. Since then, the malaria scientific community has witnessed a steady embrace of new and powerful functional genomic studies. Over the years, these approaches have slowly revolutionized malaria research and enabled the comprehensive, unbiased investigation of various aspects of the parasite's biology. These genome-wide analyses delivered a refined annotation of the parasite's genome, delivered a better knowledge of its RNA, proteins and metabolite derivatives, and fostered the discovery of new vaccine and drug targets. Despite the positive impacts of these genomic studies, most research and investment still focus on protein targets, drugs and vaccine candidates that were known before the publication of the parasite genome sequence. However, recent access to next-generation sequencing technologies, along with an increased number of genome-wide applications, is expanding the impact of the parasite genome on biomedical research, contributing to a paradigm shift in research activities that may possibly lead to new optimized diagnosis and treatments. This review provides an update of Plasmodium falciparum genome sequences and an overview of the rapid development of genomics and system biology applications that have an immense potential of creating powerful tools for a successful malaria eradication campaign.

摘要

人类疟原虫基因组的初稿于 2002 年发布。自那时以来,疟疾科学界见证了对新的强大功能基因组研究的稳步接受。多年来,这些方法逐渐彻底改变了疟疾研究,并能够全面、公正地调查寄生虫生物学的各个方面。这些全基因组分析对寄生虫基因组进行了精细化注释,增进了对其 RNA、蛋白质和代谢物衍生物的了解,并促进了新疫苗和药物靶点的发现。尽管这些基因组研究产生了积极影响,但大多数研究和投资仍集中在寄生虫基因组序列公布之前已知的蛋白质靶点、药物和疫苗候选物上。然而,最近获得的下一代测序技术以及越来越多的全基因组应用正在扩大寄生虫基因组对生物医学研究的影响,促使研究活动发生范式转变,这可能为新的优化诊断和治疗方法创造强大的工具。本综述提供了对恶性疟原虫基因组序列的更新,并概述了基因组学和系统生物学应用的快速发展,这些发展具有为成功的疟疾消除运动创造强大工具的巨大潜力。

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本文引用的文献

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Histone variant H2A.Z and RNA polymerase II transcription elongation.组蛋白变体 H2A.Z 和 RNA 聚合酶 II 转录延伸。
Mol Cell Biol. 2011 May;31(9):1848-60. doi: 10.1128/MCB.01346-10. Epub 2011 Feb 28.
2
RNA-Seq analysis of splicing in Plasmodium falciparum uncovers new splice junctions, alternative splicing and splicing of antisense transcripts.RNA-Seq 分析揭示了疟原虫中的剪接新接头、可变剪接和反义转录本剪接。
Nucleic Acids Res. 2011 May;39(9):3820-35. doi: 10.1093/nar/gkq1223. Epub 2011 Jan 17.
3
H2A.Z demarcates intergenic regions of the plasmodium falciparum epigenome that are dynamically marked by H3K9ac and H3K4me3.H2A.Z 标记恶性疟原虫表观基因组的基因间区,这些区域动态地标有 H3K9ac 和 H3K4me3。
PLoS Pathog. 2010 Dec 16;6(12):e1001223. doi: 10.1371/journal.ppat.1001223.
4
The Apicomplexan AP2 family: integral factors regulating Plasmodium development.顶复门AP2家族:疟原虫发育的重要调控因子
Mol Biochem Parasitol. 2011 Mar;176(1):1-7. doi: 10.1016/j.molbiopara.2010.11.014. Epub 2010 Nov 30.
5
HMMSplicer: a tool for efficient and sensitive discovery of known and novel splice junctions in RNA-Seq data.HMMSplicer:一种用于在 RNA-Seq 数据中高效且灵敏地发现已知和新型剪接接头的工具。
PLoS One. 2010 Nov 8;5(11):e13875. doi: 10.1371/journal.pone.0013875.
6
Identification and genome-wide prediction of DNA binding specificities for the ApiAP2 family of regulators from the malaria parasite.鉴定和全基因组预测疟原虫中 ApiAP2 家族调控因子的 DNA 结合特异性。
PLoS Pathog. 2010 Oct 28;6(10):e1001165. doi: 10.1371/journal.ppat.1001165.
7
Full-parasites: database of full-length cDNAs of apicomplexa parasites, 2010 update.全寄生虫:顶复门寄生虫全长cDNA数据库,2010年更新版
Nucleic Acids Res. 2011 Jan;39(Database issue):D625-31. doi: 10.1093/nar/gkq1111. Epub 2010 Nov 4.
8
Whole-genome sequencing and microarray analysis of ex vivo Plasmodium vivax reveal selective pressure on putative drug resistance genes.对体外培养的间日疟原虫进行全基因组测序和微阵列分析,揭示了对潜在耐药基因的选择压力。
Proc Natl Acad Sci U S A. 2010 Nov 16;107(46):20045-50. doi: 10.1073/pnas.1003776107. Epub 2010 Oct 29.
9
Metabolomics and malaria biology.代谢组学与疟疾生物学
Mol Biochem Parasitol. 2011 Feb;175(2):104-11. doi: 10.1016/j.molbiopara.2010.09.008. Epub 2010 Oct 21.
10
A genetic screen for attenuated growth identifies genes crucial for intraerythrocytic development of Plasmodium falciparum.一个遗传筛选出生长缓慢的方法,鉴定了疟原虫在红细胞内发育的关键基因。
PLoS One. 2010 Oct 11;5(10):e13282. doi: 10.1371/journal.pone.0013282.