疟疾寄生虫中不同的 RNA 聚合酶 I 转录基因对 RNA 聚合酶 I 抑制剂的抑制作用差别很大。

IF 3.3 3区 医学 Q2 MICROBIOLOGY Pathogens Pub Date : 2024-10-24 DOI:10.3390/pathogens13110924
Hermela Samuel, Riward Campelo Morillo, Björn F C Kafsack
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引用次数: 0

摘要

RNA 聚合酶 I(Pol I)转录核糖体 RNA(rRNA)是核糖体生物发生过程中的限速步骤,也是细胞生长速度的主要决定因素。与其他真核生物不同,人类疟原虫的基因组只包含少数几个单拷贝的 47S rRNA 位点,这些位点在长度、序列和在不同细胞类型中的表达上都有很大差异。我们发现,疟原虫的生长对 Pol I 抑制剂 9-hydroxyellipticine 和 BMH-21 非常敏感,并证明这两种抑制剂大大降低了 47S rRNA 的转录以及其他非编码 RNA 基因的转录。这使恶性疟原虫成为第二种RNA聚合酶I转录47S rRNA以外基因的已知生物。我们发现,各种类型的 Pol I 转录基因对这些抑制剂的敏感性相差两个数量级以上,并探讨了这些发现对恶性疟原虫 rRNA 调控的影响。
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Suppression by RNA Polymerase I Inhibitors Varies Greatly Between Distinct RNA Polymerase I Transcribed Genes in Malaria Parasites.

The transcription of ribosomal RNA (rRNA) by RNA Polymerase I (Pol I) is the rate-limiting step in ribosome biogenesis and a major determinant of cellular growth rates. Unlike other eukaryotes, which express identical rRNA from large tandem arrays of dozens to hundreds of identical rRNA genes in every cell, the genome of the human malaria parasite Plasmodium falciparum contains only a handful single-copy 47S rRNA loci that differ substantially from one another in length, sequence, and expression in different cell types. We found that the growth of the malaria parasite was acutely sensitive to the Pol I inhibitors 9-hydroxyellipticine and BMH-21 and demonstrated that they greatly reduce the transcription of 47S rRNAs as well as the transcription of other non-coding RNA genes. This makes P. falciparum only the second known organism where RNA Polymerase I transcribes genes other than the 47S rRNAs. We found that the various types of Pol I-transcribed genes differed by more than two orders of magnitude in their susceptibility to these inhibitors and explored the implications of these findings for the regulation of rRNA in P. falciparum.

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来源期刊
Pathogens
Pathogens Medicine-Immunology and Allergy
CiteScore
6.40
自引率
8.10%
发文量
1285
审稿时长
17.75 days
期刊介绍: Pathogens (ISSN 2076-0817) publishes reviews, regular research papers and short notes on all aspects of pathogens and pathogen-host interactions. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.
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