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从原生动物寄生虫 中鉴定 Ded1/DDX3 家族的 DEAD-Box RNA 解旋酶的潜在成员及其在酵母中的分析。

The Identification of Potential Members of the Ded1/DDX3 Subfamily of DEAD-Box RNA Helicases from the Protozoan Parasite and Their Analyses in Yeast.

机构信息

Expression Génétique Microbienne, UMR8261 CNRS, Université de Paris, Institut de Biologie Physico-Chimique, 13 rue Pierre et Marie Curie, 75005 Paris, France.

PSL Research University, 75005 Paris, France.

出版信息

Genes (Basel). 2021 Feb 1;12(2):212. doi: 10.3390/genes12020212.

DOI:10.3390/genes12020212
PMID:33535521
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7912733/
Abstract

DEAD-box RNA helicases are ubiquitous proteins found in all kingdoms of life and that are associated with all processes involving RNA. Their central roles in biology make these proteins potential targets for therapeutic or prophylactic drugs. The Ded1/DDX3 subfamily of DEAD-box proteins is of particular interest because of their important role(s) in translation. In this paper, we identified and aligned the protein sequences of 28 different DEAD-box proteins from the kinetoplast-protozoan parasite , which is the cause of the visceral form of leishmaniasis that is often lethal if left untreated, and compared them with the consensus sequence derived from DEAD-box proteins in general, and from the Ded1/DDX3 subfamily in particular, from a wide variety of other organisms. We identified three potential homologs of the Ded1/DDX3 subfamily and the equivalent proteins from the related protozoan parasite , which is the causative agent of sleeping sickness. We subsequently tested these proteins for their ability to complement a yeast strain deleted for the essential gene. We found that the DEAD-box proteins from Trypanosomatids are highly divergent from other eukaryotes, and consequently they are suitable targets for protein-specific drugs.

摘要

无

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/c3f664361c39/genes-12-00212-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/c3f664361c39/genes-12-00212-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/6046f5e68020/genes-12-00212-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/a8018e93a133/genes-12-00212-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/67d1a4dc48df/genes-12-00212-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/246280d63500/genes-12-00212-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d8/7912733/c3f664361c39/genes-12-00212-g005.jpg

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本文引用的文献

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2
DDX3 DEAD-box RNA helicase (Hel67) gene disruption impairs infectivity of Leishmania donovani and induces protective immunity against visceral leishmaniasis.DDX3 DEAD-box RNA 解旋酶(Hel67)基因缺失会损害利什曼原虫的感染力,并诱导对内脏利什曼病的保护性免疫。
Sci Rep. 2020 Oct 26;10(1):18218. doi: 10.1038/s41598-020-75420-y.
3
The Experimental Proteome of Promastigote and Its Usefulness for Improving Gene Annotations.
RNA 解旋酶 DDX3 的基因缺失导致翻译延伸的核糖体延伸受损,从而触发新合成多肽的共翻译质量控制。
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Recent advances and new strategies on leishmaniasis treatment.利什曼病治疗的最新进展和新策略。
Appl Microbiol Biotechnol. 2020 Nov;104(21):8965-8977. doi: 10.1007/s00253-020-10856-w. Epub 2020 Sep 2.
5
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