Suppr超能文献

RNA干扰介导的特异性基因沉默作为发现蓝氏贾第鞭毛虫新药物靶点的工具:以NADH氧化酶基因进行评估

RNAi-Mediated Specific Gene Silencing as a Tool for the Discovery of New Drug Targets in Giardia lamblia; Evaluation Using the NADH Oxidase Gene.

作者信息

Marcial-Quino Jaime, Gómez-Manzo Saúl, Fierro Francisco, Rufino-González Yadira, Ortega-Cuellar Daniel, Sierra-Palacios Edgar, Vanoye-Carlo America, González-Valdez Abigail, Torres-Arroyo Angélica, Oria-Hernández Jesús, Reyes-Vivas Horacio

机构信息

CONACYT-Instituto Nacional de Pediatría, Secretaría de Salud, Ciudad de México 04530, Mexico.

Laboratorio de Bioquímica Genética, Instituto Nacional de Pediatría, Secretaría de Salud, Ciudad de México 04530, Mexico.

出版信息

Genes (Basel). 2017 Nov 3;8(11):303. doi: 10.3390/genes8110303.

Abstract

The microaerophilic protozoan is the agent causing giardiasis, an intestinal parasitosis of worldwide distribution. Different pharmacotherapies have been employed against giardiasis; however, side effects in the host and reports of drug resistant strains generate the need to develop new strategies that identify novel biological targets for drug design. To support this requirement, we have designed and evaluated a vector containing a cassette for the synthesis of double-stranded RNA (dsRNA), which can silence expression of a target gene through the RNA interference (RNAi) pathway. Small silencing RNAs were detected and quantified in transformants expressing dsRNA by a stem-loop RT-qPCR approach. The results showed that, in transformants expressing dsRNA of 100-200 base pairs, the level of mRNA was reduced by around 30%, concomitant with a decrease in enzyme activity and a reduction in the number of trophozoites with respect to the wild type strain, indicating that NADHox is indeed an important enzyme for viability. These results suggest that it is possible to induce the RNAi machinery for attenuating the expression of genes encoding proteins of interest. We propose that our silencing strategy can be used to identify new potential drug targets, knocking down genes encoding different structural proteins and enzymes from a wide variety of metabolic pathways.

摘要

微需氧原生动物是引起贾第虫病的病原体,贾第虫病是一种在全球范围内传播的肠道寄生虫病。人们已经采用了不同的药物疗法来治疗贾第虫病;然而,宿主的副作用以及耐药菌株的报道促使人们需要开发新的策略,以确定药物设计的新生物靶点。为满足这一需求,我们设计并评估了一种载体,该载体包含一个用于合成双链RNA(dsRNA)的盒式结构,它可以通过RNA干扰(RNAi)途径使靶基因的表达沉默。通过茎环RT-qPCR方法在表达dsRNA的转化体中检测并定量了小干扰RNA。结果表明,在表达100-200个碱基对dsRNA的转化体中,mRNA水平降低了约30%,同时酶活性降低,相对于野生型菌株,滋养体数量减少,这表明NADHox确实是该生物体生存能力的一种重要酶。这些结果表明,有可能诱导RNAi机制来减弱编码感兴趣蛋白质的基因的表达。我们建议,我们的沉默策略可用于识别新的潜在药物靶点,敲低编码来自各种代谢途径的不同结构蛋白和酶的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bcb/5704216/8172a3a00ee7/genes-08-00303-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验