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RNA 降解会影响 microRNA 表达谱分析的可靠性。

RNA degradation compromises the reliability of microRNA expression profiling.

机构信息

Genomics Core Facility, EMBL, Meyerhofstrasse 1 D-69117 Heidelberg, Germany.

出版信息

BMC Biotechnol. 2009 Dec 21;9:102. doi: 10.1186/1472-6750-9-102.

Abstract

BACKGROUND

MicroRNAs are small non-coding RNAs that post-transcriptionally regulate gene expression and their expression is frequently altered in human diseases, including cancer. To correlate clinically relevant parameters with microRNA expression, total RNA is frequently prepared from samples that were archived for various time periods in frozen tissue banks but, unfortunately, RNA integrity is not always preserved in these frozen tissues. Here, we investigate whether experimentally induced RNA degradation affects microRNA expression profiles.

RESULTS

Tissue samples were maintained on ice for defined time periods prior to total RNA extraction, which resulted in different degrees of RNA degradation. MicroRNA expression was then analyzed by microarray analysis (miCHIP) or microRNA-specific real-time quantitative PCR (miQPCR). Our results demonstrate that the loss of RNA integrity leads to in unpredictability of microRNA expression profiles for both, array-based and miQPCR assays.

CONCLUSION

MicroRNA expression cannot be reliably profiled in degraded total RNA. For the profiling of microRNAs we recommend use of RNA samples with a RNA integrity number equal to or above seven.

摘要

背景

microRNAs 是小的非编码 RNA,可以在后转录水平上调节基因表达,它们的表达在包括癌症在内的人类疾病中经常发生改变。为了将临床相关参数与 microRNA 表达相关联,通常从冷冻组织库中为各种时间段存档的样本中制备总 RNA,但不幸的是,这些冷冻组织中的 RNA 完整性并不总是得到保存。在这里,我们研究了实验诱导的 RNA 降解是否会影响 microRNA 表达谱。

结果

在进行总 RNA 提取之前,将组织样本保存在冰上一段时间,导致不同程度的 RNA 降解。然后通过微阵列分析(miCHIP)或 microRNA 特异性实时定量 PCR(miQPCR)分析 microRNA 表达。我们的结果表明,RNA 完整性的丧失导致基于阵列和 miQPCR 测定的 microRNA 表达谱不可预测。

结论

在降解的总 RNA 中不能可靠地进行 microRNA 表达谱分析。对于 microRNA 的分析,我们建议使用 RNA 完整性数值等于或大于 7 的 RNA 样本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2424/2805631/4844f43aa516/1472-6750-9-102-1.jpg

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