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在感染期间,使用三个内参基因对[具体基因]进行定量实时PCR分析。

Quantitative real-time PCR analysis of and during infection, using three reference genes.

作者信息

Liew Jonathan W K, Fong Mun Yik, Lau Yee Ling

机构信息

Department of Parasitology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

出版信息

PeerJ. 2017 Jul 26;5:e3577. doi: 10.7717/peerj.3577. eCollection 2017.

Abstract

Quantitative reverse transcription PCR (qRT-PCR) has been an integral part of characterizing the immunity of mosquitoes towards invasion. Two anti- factors of , thioester-containing protein 1 (TEP1) and nitric oxide synthase (NOS), play a role in the refractoriness of towards infection and are generally expressed during infection. However, these are less studied in , a dominant malaria vector in Southeast Asia. Furthermore, most studies used a single reference gene for normalization during gene expression analysis without proper validation. This may lead to erroneous quantification of expression levels. Therefore, the present study characterized and investigated the expression profiles of and of during infection Prior to that, the (), () and () genes were validated for their suitability as a set of reference genes. and expressions in were found to be significantly induced after infection.

摘要

定量逆转录聚合酶链反应(qRT-PCR)一直是表征蚊子对入侵免疫力的一个组成部分。两种抗疟因子,即含硫酯蛋白1(TEP1)和一氧化氮合酶(NOS),在按蚊对感染的抗性中发挥作用,并且通常在感染期间表达。然而,在东南亚主要的疟疾传播媒介——按蚊中,对这些因子的研究较少。此外,大多数研究在基因表达分析过程中使用单个参考基因进行标准化,却没有进行适当的验证。这可能导致表达水平的错误定量。因此,本研究表征并研究了感染疟原虫期间按蚊中TEP1和NOS的表达谱。在此之前,对泛素延伸蛋白(UBQ)、肌动蛋白(ACT)和甘油醛-3-磷酸脱氢酶(GAPDH)基因作为一组参考基因的适用性进行了验证。发现感染疟原虫后按蚊中TEP1和NOS的表达显著上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9708/5533154/8ca565f8b0ff/peerj-05-3577-g001.jpg

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