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Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Ribosome Profiling02:24

Ribosome Profiling

Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...

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Related Experiment Video

Updated: Jun 11, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
11:44

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis

Published on: March 30, 2019

Transcriptome and targetome analysis in MIR155 expressing cells using RNA-seq.

Guorong Xu1, Claire Fewell, Christopher Taylor

  • 1Department of Computer Science, University of New Orleans, New Orleans, LA 70148, USA.

RNA (New York, N.Y.)
|June 30, 2010
PubMed
Summary
This summary is machine-generated.

Next-generation sequencing (NGS) offers superior accuracy for identifying microRNA targets compared to microarrays. This advanced technique reveals more potential targets and highlights the role of transcript structure in microRNA interactions.

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Last Updated: Jun 11, 2026

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Isolating, Sequencing and Analyzing Extracellular MicroRNAs from Human Mesenchymal Stem Cells
10:55

Isolating, Sequencing and Analyzing Extracellular MicroRNAs from Human Mesenchymal Stem Cells

Published on: March 8, 2019

Area of Science:

  • Molecular Biology
  • Genomics
  • Bioinformatics

Background:

  • Microarray analysis is a common method for identifying microRNA targets.
  • Microarrays have technical limitations in assessing transcript levels accurately.
  • Exploring microRNA targetomes requires precise transcriptomic data.

Purpose of the Study:

  • To evaluate the utility of next-generation sequencing (NGS) for microRNA target identification.
  • To compare NGS with microarray platforms for microRNA targetome analysis.
  • To investigate the role of transcript structure in microRNA-mediated gene regulation.

Main Methods:

  • Illumina-based high-throughput multiplexed NGS was used to analyze transcriptome changes.
  • Transcriptome data was analyzed to infer the microRNA targetome.
  • NGS results were compared with 3' UTR reporter assay data.
  • Transcript structure information from NGS data was used to investigate discordant results.

Main Results:

  • NGS identified a larger microRNA targetome compared to microarray studies.
  • General concordance was observed between NGS and 3' UTR reporter data.
  • Transcript structure significantly influences microRNA targeting efficacy and failure.

Conclusions:

  • NGS provides a more accurate and comprehensive approach to microRNA target identification than microarrays.
  • NGS is valuable for studying microRNA biology and mechanisms of action.
  • Understanding transcript structure is crucial for interpreting microRNA targeting effects.