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靶向顶复门原虫中共生细胞器的转录和翻译机制。

Targeting the transcriptional and translational machinery of the endosymbiotic organelle in apicomplexans.

作者信息

Fleige Tobias, Soldati-Favre Dominique

机构信息

Department of Microbiology and Molecular Medicine, CMU, University of Geneva, 1 rue Michel-Servet, 1211 Geneva 4, Switzerland.

出版信息

Curr Drug Targets. 2008 Nov;9(11):948-56. doi: 10.2174/138945008786786073.

Abstract

Apicomplexans are obligate intracellular parasites causing devastating disease in both humans and livestock. Nearly all apicomplexans, with the exception of Cryptosporidium, contain two endosymbiontic organelles carrying their own DNA; the mitochondrion and the plastid-like organelle called the apicoplast. The apicoplast is an attractive drug target as it harbors not only metabolic pathways not found in the host cell, but it is also dependent on its ancient transcriptional and translational machinery. These parasites rely on the plastid, and inhibition of its function or loss of this organelle leads to immediate or delayed death. Replication of plastidic DNA shows differences between the members of this phylum. In Plasmodium parasites, two forms of replication are observed--unidirectional single-stranded replication and a rolling circle mechanism--whereas in Toxoplasma gondii only the rolling circle is found. Targeting enzymes involved in DNA-replication leads to a delayed death of the parasite. Most of the genes in the apicoplast genome encode elements of their own transcriptional and translational machinery, and they are highly similar to those found in bacteria. Several anti-bacterials which target this machinery are also active against apicomplexan parasites and inhibition leads mostly to the delayed death phenomenon.

摘要

顶复门原虫是专性细胞内寄生虫,可在人类和家畜中引发毁灭性疾病。除隐孢子虫外,几乎所有顶复门原虫都含有两个携带自身DNA的内共生细胞器;线粒体和类似质体的细胞器,即顶质体。顶质体是一个有吸引力的药物靶点,因为它不仅含有宿主细胞中不存在的代谢途径,而且还依赖于其古老的转录和翻译机制。这些寄生虫依赖质体,抑制其功能或失去这个细胞器会导致立即或延迟死亡。质体DNA的复制在该门的成员之间存在差异。在疟原虫中,观察到两种复制形式——单向单链复制和滚环机制——而在刚地弓形虫中只发现了滚环机制。靶向参与DNA复制的酶会导致寄生虫延迟死亡。顶质体基因组中的大多数基因编码其自身转录和翻译机制的元件,并且它们与细菌中的元件高度相似。几种靶向这种机制的抗菌药物对顶复门原虫寄生虫也有活性,抑制作用大多导致延迟死亡现象。

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