Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

The double-stranded RNA-binding motif, a versatile macromolecular docking platform.

Kung-Yao Chang1, Andres Ramos

  • 1Institute of Biochemistry, National Chung-Hsing University, Taichung, Taiwan. kychang@dragon.nchu.edu.tw

The FEBS Journal
|April 28, 2005
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Cracking the (zip)code of dynein-dependent RNA localization.

Nature structural & molecular biology·2026
Same author

Polypeptide encoded by the -1 PRF signal of SARS-CoV-2 controls multiple enzymatic activities of the viral NiRAN domain.

NAR molecular medicine·2025
Same author

Decoding the interactions and functions of non-coding RNA with artificial intelligence.

Nature reviews. Molecular cell biology·2025
Same author

m6A modification inhibits miRNAs' intracellular function, favoring their extracellular export for intercellular communication.

Cell reports·2024
Same author

m6a methylation orchestrates IMP1 regulation of microtubules during human neuronal differentiation.

Nature communications·2024
Same author

From the Operating Room to the Laboratory: Role of the Neuroscience Tissue Biorepository in the Clinical, Translational, and Basic Science Research Pipeline.

Mayo Clinic proceedings·2024

The double-stranded RNA-binding motif (dsRBM) recognizes structured RNA via two distinct modes. Recent studies reveal dsRBMs also bind proteins and DNA, expanding their regulatory roles.

Area of Science:

  • Molecular Biology
  • Structural Biology
  • Biochemistry

Background:

  • The double-stranded RNA-binding motif (dsRBM) is a conserved protein domain found across eukaryotes, bacteria, and viruses.
  • dsRBMs are crucial for various cellular processes, including RNA editing and translational control, often appearing in multiple copies within a protein.

Purpose of the Study:

  • To elucidate the structural mechanisms of RNA target recognition by dsRBMs.
  • To explore the broader functional roles and interaction capabilities of dsRBM-containing proteins.

Main Methods:

  • Structural analysis of dsRBM-RNA interactions.
  • Investigation of dsRBM binding to non-RNA targets.

Main Results:

  • Identified two primary modes of RNA binding by dsRBMs: recognition of RNA helix moieties and interaction with flanking RNA duplex elements.

Related Experiment Videos

  • Demonstrated that dsRBMs can bind to proteins and DNA, in addition to RNA.
  • Highlighted the regulatory role of dsRBMs in catalytic processes, often in conjunction with other protein domains.
  • Conclusions:

    • dsRBMs exhibit versatile RNA recognition strategies and can interact with diverse molecular targets.
    • Further research is needed to understand the functional interplay between different dsRBMs and the principles governing dsRBM-protein interactions for elucidating complex regulatory networks.