顶复合体和着丝体寄生虫核糖核蛋白复合物中RNA m6A甲基化的动态调控。

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kaitlin Klotz, Carli Camporeale, Kausik Chakrabarti
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引用次数: 0

摘要

m6A,或n6 -甲基腺苷,是mRNA转录物中最丰富的修饰。已知这些修饰会影响mRNA转录物的稳定性、转录、翻译、选择性剪接和衰变,无疑还有更多的功能有待发现。在这篇综述中,我们探讨了m6A修饰在两类原生动物寄生虫中的作用:包括疟原虫和弓形虫在内的顶复体,以及包括锥虫和利什曼原虫在内的动质体。我们还比较了m6A表转录组机制的关键参与者,在这些寄生原生生物之间产生、解释和去除m6A修饰,并讨论了m6A修饰如何通过顶复合体和着丝质体的特异性特征促进寄生虫的生存。除了寄生虫的表转录组外,本文还比较了宿主和媒介物种(人类、苍蝇和蚊子)中的m6A动态,强调了共同进化适应。引人注目的是,寄生虫和它们的载体都缺乏典型的m6A去甲基化酶,这意味着一个基本上不可逆的、流线型的m6A景观被微调为同步基因调控。总的来说,关于m6a修饰的RNA及其结合蛋白如何在寄生原生生物中协调RNA加工、翻译和转换的机制理解正在出现,揭示了一个进化调谐的表转录组系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamic Regulation of RNA m6A Methylation in the Ribonucleoprotein Complexes in Apicomplexan and Kinetoplastid Parasites.

m6A, or N6-methyladenosine, is a the most abundant modification of mRNA transcripts. These modifications are known to influence mRNA transcript stability, transcription, translation, alternative splicing and decay, with undoubtedly more functions to be discovered. In this review, we explored the roles of m6A modifications in two groups of protozoan parasites: the apicomplexans, which include Plasmodium and Toxoplasma species, and kinetoplastids, which include Trypanosoma and Leishmania species. We also compared the key players of m6A epitranscriptomic machinery in creating, interpreting, and removing m6A modifications between these parasitic protists as well as a discussion of how m6A modifications facilitate parasite survival through features specific to apicomplexans and kinetoplastids. Beyond parasite epitranscriptomes, this review compares m6A dynamics in host and vector species (humans, flies and mosquitoes), highlighting coevolutionary adaptations. Strikingly, both the parasites and their vectors lack canonical m6A demethylases, implying a largely irreversible, streamlined m6A landscape fine-tuned for synchronized gene regulation. Overall, a mechanistic understanding is emerging of how m6A-modified RNAs and their binding proteins orchestrate RNA processing, translation, and turnover in parasitic protists, revealing an evolutionarily tuned epitranscriptomic system.

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来源期刊
Biomedical Journal
Biomedical Journal Medicine-General Medicine
CiteScore
11.60
自引率
1.80%
发文量
128
审稿时长
42 days
期刊介绍: Biomedical Journal publishes 6 peer-reviewed issues per year in all fields of clinical and biomedical sciences for an internationally diverse authorship. Unlike most open access journals, which are free to readers but not authors, Biomedical Journal does not charge for subscription, submission, processing or publication of manuscripts, nor for color reproduction of photographs. Clinical studies, accounts of clinical trials, biomarker studies, and characterization of human pathogens are within the scope of the journal, as well as basic studies in model species such as Escherichia coli, Caenorhabditis elegans, Drosophila melanogaster, and Mus musculus revealing the function of molecules, cells, and tissues relevant for human health. However, articles on other species can be published if they contribute to our understanding of basic mechanisms of biology. A highly-cited international editorial board assures timely publication of manuscripts. Reviews on recent progress in biomedical sciences are commissioned by the editors.
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