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用于云杉芽卷叶蛾核多角体病毒(CfMNPV)基因转录分析的基于寡核苷酸的DNA微阵列的开发。

Development of an oligonucleotide-based DNA microarray for transcriptional analysis of Choristoneura fumiferana nucleopolyhedrovirus (CfMNPV) genes.

作者信息

Yang Dan-Hui, Barari Mehrnoosh, Arif Basil M, Krell Peter J

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ont. N1G 2W1, Canada.

出版信息

J Virol Methods. 2007 Aug;143(2):175-85. doi: 10.1016/j.jviromet.2007.03.007. Epub 2007 Apr 10.

Abstract

A modified oligonucleotide-based two-channel DNA microarray was developed for characterization of temporal expression profiles of select Choristoneura fumiferana nucleopolyhedrovirus (CfMNPV) ORFs including its 7 unique ORFs. The microarray chip contained oligonucleotide probes for 23 CfMNPV ORFs and their complements as well as five host genes. Total RNA was isolated at different times post infection from Cf203 insect cells infected with CfMNPV. The cDNA was synthesized, fluorescent labelled with Cy3, and co-hybridized to the microarray chips along with Cy5-labelled viral genomic DNA, which served as equimolar reference standards for each probe. Transcription of the 7 CfMNPV unique ORFs was detected using DNA microarray analysis and their temporal expression profiles suggest that they are functional genes. The expression levels of three host genes varied throughout virus infection and therefore were unsuitable for normalization between microarrays. The DNA microarray results were compared to quantitative RT-PCR (qRT-PCR). Transcription of the non-coding (antisense) strands of some of the CfMNPV select genes including the polyhedrin gene, was also detected by array analysis and confirmed by qRT-PCR. The polyhedrin antisense transcript, based on long-range RT-PCR analysis, appeared to be a read-through product of an adjacent ORF in the same orientation as the antisense transcript.

摘要

开发了一种基于寡核苷酸的改良型双通道DNA微阵列,用于表征选定的云杉色卷蛾核多角体病毒(CfMNPV)开放阅读框(ORF)的时间表达谱,包括其7个独特的ORF。微阵列芯片包含针对23个CfMNPV ORF及其互补序列以及五个宿主基因的寡核苷酸探针。在感染CfMNPV的Cf203昆虫细胞感染后的不同时间分离总RNA。合成cDNA,用Cy3进行荧光标记,并与作为每个探针等摩尔参考标准的Cy5标记的病毒基因组DNA一起与微阵列芯片共杂交。使用DNA微阵列分析检测7个CfMNPV独特ORF的转录,其时间表达谱表明它们是功能基因。三个宿主基因的表达水平在病毒感染过程中有所变化,因此不适合用于微阵列之间的标准化。将DNA微阵列结果与定量逆转录聚合酶链反应(qRT-PCR)进行比较。通过阵列分析还检测到了一些CfMNPV选定基因(包括多角体蛋白基因)非编码(反义)链的转录,并通过qRT-PCR得到证实。基于长距离RT-PCR分析,多角体蛋白反义转录本似乎是与反义转录本方向相同的相邻ORF的通读产物。

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