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人全唾液中 microRNA 特征的高分辨率

High resolution of microRNA signatures in human whole saliva.

机构信息

Department of Oral Biology, University of Florida College of Dentistry, Gainesville, FL 32610, USA.

出版信息

Arch Oral Biol. 2011 Dec;56(12):1506-13. doi: 10.1016/j.archoralbio.2011.05.015. Epub 2011 Jun 24.

Abstract

OBJECTIVE

Identifying discriminatory human salivary RNA biomarkers reflective of disease in a low-cost non-invasive screening assay is crucial to salivary diagnostics. Recent studies have reported both mRNA and microRNA (miRNA) in saliva, but little information has been documented on the quality and yield of RNA collected. Therefore, the aim of the present study was to develop an improved RNA isolation method from saliva and to identify major miRNA species in human whole saliva.

DESIGN

RNA samples were isolated from normal human saliva using a combined protocol based on the Oragene RNA collection kit and the mirVana miRNA isolation kit in tandem. RNA samples were analysed for quality and subjected to miRNA array analysis.

RESULTS

RNA samples isolated from twenty healthy donors ranged from 2.59 to 29.4 μg/ml saliva and with 1.92-2.16OD(260/280 nm) ratios. RNA yield and concentration of saliva samples were observed to be stable over 48 h at room temperature. Analysis of total salivary RNA isolated from these twenty donors showed no statistical significance between sexes; however, the presence of high-, medium-, and low-yield salivary RNA producers was detected. MiRNA array analysis of salivary RNA detected five abundantly expressed miRNAs, miR-223, miR-191, miR-16, miR-203, and miR-24, that were similarly described in other published reports. Additionally, many previously undetected miRNAs were also identified.

CONCLUSION

High quality miRNAs can be isolated from saliva using available commercial kits, and in future studies, the availability of this isolation protocol may allow specific changes in their levels to be measured accurately in various relevant diseases.

摘要

目的

在低成本、非侵入性的筛选检测中,识别反映疾病的具有歧视性的人类唾液 RNA 生物标志物对于唾液诊断至关重要。最近的研究已经在唾液中报告了 mRNA 和 microRNA (miRNA),但关于收集到的 RNA 的质量和产量的信息很少有记录。因此,本研究的目的是开发一种从唾液中提取 RNA 的改良方法,并鉴定人全唾液中的主要 miRNA 种类。

设计

使用基于 Oragene RNA 收集试剂盒和 mirVana miRNA 分离试剂盒的组合方案,从正常人类唾液中分离 RNA 样品。对 RNA 样品进行质量分析,并进行 miRNA 阵列分析。

结果

从二十名健康供体中分离的 RNA 样品的范围为 2.59 至 29.4μg/ml 唾液,并且 1.92-2.16OD(260/280nm) 比值。在室温下,观察到唾液样品的 RNA 产量和浓度在 48 小时内稳定。从这二十名供体中分离的总唾液 RNA 的分析显示,性别之间没有统计学意义;然而,检测到高、中、低产量唾液 RNA 产生者的存在。唾液 RNA 的 miRNA 阵列分析检测到五个高度表达的 miRNA,miR-223、miR-191、miR-16、miR-203 和 miR-24,这些 miRNA 在其他已发表的报告中也有类似描述。此外,还鉴定出许多以前未检测到的 miRNA。

结论

使用现有的商业试剂盒可以从唾液中分离出高质量的 miRNA,在未来的研究中,这种分离方案的可用性可能允许在各种相关疾病中准确测量其水平的特定变化。

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