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一种用于顶复门寄生虫中条件性基因表达控制的工具盒。

A toolbox for conditional control of gene expression in apicomplexan parasites.

机构信息

INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses, Sorbonne Université, Paris, France.

CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, CIIL, Univ. Lille, Lille, France.

出版信息

Mol Microbiol. 2022 Mar;117(3):618-631. doi: 10.1111/mmi.14821. Epub 2021 Oct 13.

DOI:10.1111/mmi.14821
PMID:34564906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9293482/
Abstract

Apicomplexan parasites encompass diverse pathogens for humans and animals, including the causative agents of malaria and toxoplasmosis, Plasmodium spp. and Toxoplasma gondii. Genetic manipulation of these parasites has become central to explore parasite biology, unravel gene function and identify new targets for therapeutic strategies. Tremendous progress has been achieved over the past years with the advent of next generation sequencing and powerful genome editing methods. In particular, various methods for conditional gene expression have been developed in both Plasmodium and Toxoplasma to knockout or knockdown essential genes, or for inducible expression of master developmental regulators or mutant versions of proteins. Conditional gene expression can be achieved at three distinct levels. At the DNA level, inducible site-specific recombinases allow conditional genome editing. At the RNA level, regulation can be achieved during transcription, using stage-specific or regulatable promoters, or post-transcriptionally through alteration of mRNA stability or translation. At the protein level, several systems have been developed for inducible degradation or displacement of a protein of interest. In this review, we provide an overview of current systems for conditional control of gene expression in Plasmodium and Toxoplasma parasites, highlighting the advantages and limitations of each approach.

摘要

顶复门寄生虫包括多种人类和动物病原体,包括疟疾和弓形体病的病原体,疟原虫属和刚地弓形虫。这些寄生虫的遗传操作已成为探索寄生虫生物学、揭示基因功能和确定新的治疗策略靶点的核心手段。随着下一代测序和强大的基因组编辑方法的出现,近年来取得了巨大的进展。特别是,在疟原虫和弓形虫中已经开发了各种条件性基因表达方法,以敲除或敲低必需基因,或诱导表达主要发育调节剂或蛋白质的突变体。条件性基因表达可以在三个不同的水平上实现。在 DNA 水平上,诱导型位点特异性重组酶允许条件性基因组编辑。在 RNA 水平上,可以通过使用阶段特异性或可调节启动子在转录过程中进行调控,或者通过改变 mRNA 稳定性或翻译进行转录后调控。在蛋白质水平上,已经开发了几种系统来诱导靶蛋白的降解或置换。在这篇综述中,我们概述了疟原虫和弓形虫寄生虫中条件性基因表达控制的当前系统,强调了每种方法的优点和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/145ec03834d3/MMI-117-618-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/17b7d1c5f9f9/MMI-117-618-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/059efa74bbef/MMI-117-618-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/145ec03834d3/MMI-117-618-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/17b7d1c5f9f9/MMI-117-618-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/059efa74bbef/MMI-117-618-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d504/9293482/145ec03834d3/MMI-117-618-g001.jpg

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3
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