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通过Northern印迹法检测和验证哺乳动物的微小内含子

Detection and Verification of Mammalian Mirtrons by Northern Blotting.

作者信息

Zia Mohammad Farid, Flynt Alex S

机构信息

Department of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS, USA.

出版信息

Methods Mol Biol. 2018;1823:209-219. doi: 10.1007/978-1-4939-8624-8_16.

Abstract

microRNAs (miRNAs) have vital roles in regulating gene expression-contributing to major diseases like cancer and heart disease. Over the last decade, thousands of miRNAs have been discovered through high throughput sequencing-based annotation. Different classes have been described, as well as a great dynamic range of expression levels. While sequencing approaches provide insight into biogenesis and allow confident identification, there is a need for additional methods for validation and characterization. Northern blotting was one of the first techniques used for studying miRNAs, and remains one of the most valuable as it avoids enzymatic manipulation of miRNA transcripts. Blotting can also provide insight into biogenesis by revealing RNA processing intermediates. Compared to sequencing, however, northern blotting is a relatively insensitive technology. This creates a challenge for detecting low expressed miRNAs, particularly those produced by inefficient, non-canonical pathways. In this chapter, we describe a strategy to study such miRNAs by northern blotting that involves ectopic expression of both miRNAs and miRNA-binding Argonaute (Ago) proteins. Through use of epitope tags, this strategy also provides a convenient method for verification of small RNA competency to be loaded into regulatory complexes.

摘要

微小RNA(miRNA)在调节基因表达中发挥着至关重要的作用,与癌症和心脏病等重大疾病相关。在过去十年中,通过基于高通量测序的注释发现了数千种miRNA。已经描述了不同的类别,以及表达水平的巨大动态范围。虽然测序方法有助于深入了解生物发生过程并能可靠地鉴定miRNA,但仍需要其他方法进行验证和表征。Northern印迹法是最早用于研究miRNA的技术之一,并且仍然是最有价值的技术之一,因为它避免了对miRNA转录本进行酶处理。印迹法还可以通过揭示RNA加工中间体来深入了解生物发生过程。然而,与测序相比,Northern印迹法是一种相对不灵敏的技术。这给检测低表达的miRNA带来了挑战,尤其是那些由低效、非经典途径产生的miRNA。在本章中,我们描述了一种通过Northern印迹法研究此类miRNA的策略,该策略涉及miRNA和与miRNA结合的AGO蛋白的异位表达。通过使用表位标签,该策略还提供了一种方便的方法来验证小RNA加载到调节复合物中的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07ec/6276377/9b70bf0fae20/nihms-989211-f0001.jpg

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