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疟疾表观遗传学

Malaria Epigenetics.

作者信息

Cortés Alfred, Deitsch Kirk W

机构信息

ISGlobal, Barcelona Centre for International Health Research (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Catalonia 08036, Spain.

ICREA, Barcelona, Catalonia 08010, Spain.

出版信息

Cold Spring Harb Perspect Med. 2017 Jul 5;7(7):a025528. doi: 10.1101/cshperspect.a025528.

DOI:10.1101/cshperspect.a025528
PMID:28320828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5495052/
Abstract

Organisms with identical genome sequences can show substantial differences in their phenotypes owing to epigenetic changes that result in different use of their genes. Epigenetic regulation of gene expression plays a key role in the control of several fundamental processes in the biology of malaria parasites, including antigenic variation and sexual differentiation. Some of the histone modifications and chromatin-modifying enzymes that control the epigenetic states of malaria genes have been characterized, and their functions are beginning to be unraveled. The fundamental principles of epigenetic regulation of gene expression appear to be conserved between malaria parasites and model eukaryotes, but important peculiarities exist. Here, we review the current knowledge of malaria epigenetics and discuss how it can be exploited for the development of new molecular markers and new types of drugs that may contribute to malaria eradication efforts.

摘要

具有相同基因组序列的生物体可能由于表观遗传变化而在表型上表现出显著差异,表观遗传变化导致其基因的不同利用方式。基因表达的表观遗传调控在疟原虫生物学的几个基本过程的控制中起着关键作用,包括抗原变异和性别分化。一些控制疟疾基因表观遗传状态的组蛋白修饰和染色质修饰酶已被鉴定,其功能也开始被揭示。基因表达表观遗传调控的基本原理在疟原虫和模式真核生物之间似乎是保守的,但也存在重要的独特之处。在这里,我们综述了当前关于疟疾表观遗传学的知识,并讨论了如何利用它来开发新的分子标记和新型药物,这些可能有助于疟疾根除工作。

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本文引用的文献

1
Plasmodium falciparum PfSET7: enzymatic characterization and cellular localization of a novel protein methyltransferase in sporozoite, liver and erythrocytic stage parasites.恶性疟原虫PfSET7:一种新型蛋白质甲基转移酶在子孢子、肝脏和红细胞期疟原虫中的酶学特性及细胞定位
Sci Rep. 2016 Feb 23;6:21802. doi: 10.1038/srep21802.
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The nucleosome landscape of Plasmodium falciparum reveals chromatin architecture and dynamics of regulatory sequences.恶性疟原虫的核小体图谱揭示了染色质结构和调控序列的动态变化。
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Dual regulatory effects of non-coding GC-rich elements on the expression of virulence genes in malaria parasites.富含GC的非编码元件对疟原虫毒力基因表达的双重调控作用。
Infect Genet Evol. 2015 Dec;36:490-499. doi: 10.1016/j.meegid.2015.08.023. Epub 2015 Aug 20.
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Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes.解读控制恶性疟原虫clag3基因相互排斥表达的原理。
Nucleic Acids Res. 2015 Sep 30;43(17):8243-57. doi: 10.1093/nar/gkv730. Epub 2015 Jul 21.
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Mosquitoes Reset Malaria Parasites.蚊子重置疟原虫。
PLoS Pathog. 2015 Jul 2;11(7):e1004987. doi: 10.1371/journal.ppat.1004987. eCollection 2015 Jul.
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Strand-specific RNA sequencing in Plasmodium falciparum malaria identifies developmentally regulated long non-coding RNA and circular RNA.恶性疟原虫疟疾中的链特异性RNA测序鉴定出发育调控的长链非编码RNA和环状RNA。
BMC Genomics. 2015 Jun 13;16(1):454. doi: 10.1186/s12864-015-1603-4.
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A Plasmodium Falciparum Bromodomain Protein Regulates Invasion Gene Expression.恶性疟原虫溴结构域蛋白调控入侵基因表达。
Cell Host Microbe. 2015 Jun 10;17(6):741-51. doi: 10.1016/j.chom.2015.05.009.
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A Unique Virulence Gene Occupies a Principal Position in Immune Evasion by the Malaria Parasite Plasmodium falciparum.一个独特的毒力基因在恶性疟原虫逃避免疫过程中占据主要地位。
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