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Related Concept Videos

Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

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RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
All three eukaryotic RNAPs require specific transcription factors, of which the...
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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. 
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Related Experiment Video

Updated: May 3, 2026

Capture and Identification of RNA-binding Proteins by Using Click Chemistry-assisted RNA-interactome Capture CARIC Strategy
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Capture and Identification of RNA-binding Proteins by Using Click Chemistry-assisted RNA-interactome Capture CARIC Strategy

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Tracking RNA polymerase, one step at a time.

Dmitry G Vassylyev1, Irina Artsimovitch

  • 1Department of Biochemistry and Molecular Genetics, University of Alabama, Birmingham, Alabama 35294, USA.

Cell
|December 20, 2005
PubMed
Summary

Researchers found that bacterial RNA polymerase moves in single base-pair steps. This enzyme functions as a Brownian ratchet, propelled by nucleoside triphosphate binding during transcription.

Area of Science:

  • Molecular Biology
  • Biophysics

Background:

  • Structural analysis of transcription has achieved high resolution.
  • Techniques for manipulating single molecules in transcription have been limited.

Purpose of the Study:

  • To develop and apply single-molecule manipulation techniques to study transcription.
  • To elucidate the step-wise mechanism of bacterial RNA polymerase during transcription.

Main Methods:

  • Utilized single-molecule force spectroscopy to measure the movement of individual bacterial RNA polymerase molecules.
  • Analyzed the step size and dynamics of polymerase translocation along DNA.

Main Results:

  • Demonstrated that bacterial RNA polymerase translocates in discrete, single base-pair steps.

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  • Observed that the binding of incoming nucleoside triphosphates drives polymerase forward motion.
  • Conclusions:

    • Bacterial RNA polymerase functions as a Brownian ratchet.
    • The binding energy of nucleotides is converted into mechanical work to drive transcription progression.