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单侧输尿管梗阻小鼠肾脏中微小RNA表达的定量实时聚合酶链反应评估

Quantitative Real-Time PCR Evaluation of microRNA Expressions in Mouse Kidney with Unilateral Ureteral Obstruction.

作者信息

Yanai Katsunori, Kaneko Shohei, Ishii Hiroki, Aomatsu Akinori, Ito Kiyonori, Hirai Keiji, Ookawara Susumu, Ishibashi Kenichi, Morishita Yoshiyuki

机构信息

Division of Nephrology, First Department of Integrated Medicine, Saitama Medical Center, Jichi Medical University.

Division of Nephrology, First Department of Integrated Medicine, Saitama Medical Center, Jichi Medical University; Division of Intensive Care Unit, First Department of Integrated Medicine, Saitama Medical Center, Jichi Medical University.

出版信息

J Vis Exp. 2020 Aug 27(162). doi: 10.3791/61383.

Abstract

MicroRNAs (miRNAs) are single stranded, non-coding RNA molecules that typically regulate gene expression at the post-transcriptional level by binding to partially complementary target sites in the 3' untranslated region (UTR) of messenger RNA (mRNA), which reduces the mRNA's translation and stability. The miRNA expression profiles in various organs and tissues of mice have been investigated, but standard methods for the purification and quantification of miRNA in mouse kidney have not been available. We have established an effective and reliable method for extracting and evaluating miRNA expression in mouse kidney with renal interstitial fibrosis by quantitative reverse-transcription polymerase chain reaction (qRT-PCR). The protocol required five steps: (1) creation of sham and unilateral ureteral obstruction (UUO) mice; (2) extraction of kidney samples from the UUO mice; (3) extraction of total RNA, which includes miRNA, from the kidney samples; (4) complementary DNA (cDNA) synthesis with reverse transcription from miRNA; and (5) qRT-PCR using the cDNA. Using this protocol, we successfully confirmed that compared to the controls, the expression of miRNA-3070-3p was significantly increased and those of miRNA-7218-5p and miRNA-7219-5p were significantly decreased in the kidneys of a mouse model of renal interstitial fibrosis. This protocol can be used to determine the miRNA expression in the kidneys of mice with UUO.

摘要

微小RNA(miRNA)是单链非编码RNA分子,通常通过与信使RNA(mRNA)的3'非翻译区(UTR)中部分互补的靶位点结合,在转录后水平调节基因表达,这会降低mRNA的翻译和稳定性。已经对小鼠各种器官和组织中的miRNA表达谱进行了研究,但尚未有用于纯化和定量小鼠肾脏中miRNA的标准方法。我们建立了一种有效且可靠的方法,通过定量逆转录聚合酶链反应(qRT-PCR)提取和评估肾间质纤维化小鼠肾脏中的miRNA表达。该方案需要五个步骤:(1)创建假手术和单侧输尿管梗阻(UUO)小鼠;(2)从UUO小鼠中提取肾脏样本;(3)从肾脏样本中提取包括miRNA在内的总RNA;(4)通过miRNA逆转录合成互补DNA(cDNA);(5)使用cDNA进行qRT-PCR。使用该方案,我们成功证实,与对照组相比,在肾间质纤维化小鼠模型的肾脏中,miRNA-3070-3p的表达显著增加,而miRNA-7218-5p和miRNA-7219-5p的表达显著降低。该方案可用于确定UUO小鼠肾脏中的miRNA表达。

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