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通过将总RNA与寡核苷酸阵列杂交进行细菌转录本成像。

Bacterial transcript imaging by hybridization of total RNA to oligonucleotide arrays.

作者信息

de Saizieu A, Certa U, Warrington J, Gray C, Keck W, Mous J

机构信息

Pharma Division, F. Hoffmann-La Roche Ltd., Basel, Switzerland.

出版信息

Nat Biotechnol. 1998 Jan;16(1):45-8. doi: 10.1038/nbt0198-45.

Abstract

We have used high-density oligonucleotide probe arrays (chips) for bacterial transcript imaging. We designed a chip containing probes representing 106 Hemophilus influenzae genes and 100 Streptococcus pneumoniae genes. The apparent lack of polyadenylated transcripts excludes enrichment of mRNA by affinity purification and we thus used total, chemically biotinylated RNA as hybridization probe. We show that hybridization of Streptococcus RNA to a chip allows simultaneous quantification of the transcript levels. The sensitivity was found to be in the range of one to five transcripts per cell. The quantitative chip results were in good agreement with conventional Northern blot analysis of selected genes. This technology allows simultaneous and quantitative measurement of the transcriptional activity of entire bacterial genomes on a single oligonucleotide probe array.

摘要

我们已将高密度寡核苷酸探针阵列(芯片)用于细菌转录成像。我们设计了一种芯片,其中包含代表106个流感嗜血杆菌基因和100个肺炎链球菌基因的探针。明显缺乏聚腺苷酸化转录本排除了通过亲和纯化富集mRNA的可能性,因此我们使用经化学生物素化的总RNA作为杂交探针。我们表明,链球菌RNA与芯片的杂交可同时定量转录本水平。发现灵敏度在每个细胞1至5个转录本的范围内。芯片定量结果与所选基因的传统Northern印迹分析结果高度一致。这项技术能够在单个寡核苷酸探针阵列上同时定量测量整个细菌基因组的转录活性。

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