4.8 Article

FASTmiR: an RNA-based sensor for in vitro quantification and live-cell localization of small RNAs

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NUCLEIC ACIDS RESEARCH
卷 45, 期 14, 页码 -

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OXFORD UNIV PRESS
DOI: 10.1093/nar/gkx504

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资金

  1. U.S. National Science Foundation (NSF) via an 'EAGER' Award [1252939]
  2. NSF Plant Genome Research Program [1339229]
  3. National Institutes of Health [1R41GM110877, 1R41GM097811]
  4. NIH-NIGMS [P20 GM103446, S10 OD016361]
  5. NSF [EPSCoR] [IIA-1301765]
  6. NSF IOS Award [1339229]
  7. Direct For Biological Sciences
  8. Div Of Molecular and Cellular Bioscience [1252939] Funding Source: National Science Foundation
  9. Division Of Integrative Organismal Systems
  10. Direct For Biological Sciences [1649424] Funding Source: National Science Foundation

向作者/读者索取更多资源

Small RNAs, including microRNAs (miRNAs) and small interfering RNAs (siRNAs), play a variety of important regulatory roles in many eukaryotes. Their small size has made it challenging to study them directly in live cells. Here we describe an RNA-based fluorescent sensor for small RNA detection both in vitro and in vivo, adaptable for any small RNA. It utilizes an sxRNA switch for detection of miRNA-mRNA interactions combined with a fluorophore-binding sequence 'Spinach', a GFP-like RNA aptamer for which the RNA-fluorophore complex exhibits strong and consistent fluorescence under an excitation wavelength. Two example sensors, FASTmiR171 and FASTmiR122, can rapidly detect and quantify the levels of miR171 and miR122 in vitro. The sensors can determine relative levels of miRNAs in total RNA extracts with sensitivity similar to small RNA sequencing and northern blots. FASTmiR sensors were also used to estimate the copy number range of miRNAs in total RNA extracts. To localize and analyze the spatial distribution of small RNAs in live, single cells, tandem copies of FASTmiR122 were expressed in different cell lines. FASTmiR122 was able to quantitatively detect the differences in miR122 levels in Huh7 and HEK293T cells demonstrating its potential for tracking miRNA expression and localization in vivo.

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