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Related Concept Videos

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 18, 2026

A Rapid High-throughput Method for Mapping Ribonucleoproteins (RNPs) on Human pre-mRNA
13:00

A Rapid High-throughput Method for Mapping Ribonucleoproteins (RNPs) on Human pre-mRNA

Published on: December 2, 2009

High-throughput sequencing methods to study neuronal RNA-protein interactions.

Jernej Ule1

  • 1MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK. jule@mrc-lmb.cam.ac.uk

Biochemical Society Transactions
|November 14, 2009
PubMed
Summary
This summary is machine-generated.

High-throughput sequencing methods like UV-cross-linking and immunoprecipitation (UV-CLIP) map RNA-protein interactions. These techniques offer insights into post-transcriptional regulation in neurons and RNP remodelling dynamics.

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Area of Science:

  • Molecular Biology
  • Neuroscience
  • Genomics

Background:

  • Post-transcriptional regulation is crucial for neuronal function, particularly in synaptic plasticity.
  • High-throughput sequencing methods have enabled global mapping of RNA-protein interactions.

Purpose of the Study:

  • To explore the application of UV-cross-linking and immunoprecipitation (UV-CLIP) for identifying RNA binding sites of splicing regulators.
  • To discuss the potential of ribosome profiling and other high-throughput methods in studying neuronal post-transcriptional regulation dynamics.

Main Methods:

  • UV-cross-linking and RNase protection coupled with high-throughput sequencing.
  • UV-cross-linking and immunoprecipitation (UV-CLIP) with stringent purification protocols.
  • Ribosome profiling for quantifying ribosome density on mRNAs.

Main Results:

  • UV-CLIP successfully identified intronic and exonic sites bound by splicing regulators in mouse brain tissue.
  • Ribosome profiling quantified ribosome density on yeast mRNAs under varying environmental conditions.

Conclusions:

  • High-throughput sequencing techniques provide powerful tools for mapping RNA-protein interactions.
  • Further application of these biochemical techniques is expected to yield significant insights into neuronal post-transcriptional regulation mechanisms.