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 Concept Videos

Nuclear Export of mRNA02:31

Nuclear Export of mRNA

7.1K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
7.1K
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

4.7K
4.7K
RNA Splicing01:32

RNA Splicing

53.3K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
53.3K
RNA Splicing01:32

RNA Splicing

15.9K
15.9K
Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

17.3K
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...
17.3K
Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

8.4K
8.4K

You might also read

Related Articles

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

Sort by
Same author

The E3-ome gene-centric compendium reveals the human E3 ligase landscape.

Cell·2026
Same author

Structural basis for a nucleoporin exportin complex between RanBP2, SUMO1-RanGAP1, the E2 Ubc9, Crm1 and the Ran GTPase.

Nature communications·2025
Same author

Structural basis for a nucleoporin exportin complex between RanBP2, SUMO1-RanGAP1, the E2 Ubc9, Crm1 and the Ran GTPase.

bioRxiv : the preprint server for biology·2025
Same author

Chemical Tools for Probing the Ub/Ubl Conjugation Cascades.

Chembiochem : a European journal of chemical biology·2024
Same author

Structural basis for transthiolation intermediates in the ubiquitin pathway.

Nature·2024
Same author

Design and Semisynthesis of Biselectrophile-Functionalized Ubiquitin Probes To Investigate Transthioesterification Reactions.

Organic letters·2024
Same journal

Tomogram exploration through template matching and deep learning.

Current opinion in structural biology·2026
Same journal

A comparative review of cryo-electron ptychography: Biological applications and future perspectives.

Current opinion in structural biology·2026
Same journal

Metabolic disruptions through a three-dimensional genomic lens.

Current opinion in structural biology·2026
Same journal

Collective variable design for biomolecular conformational dynamics.

Current opinion in structural biology·2026
Same journal

Polymer scaling in protein crowding: From dilute coils to semidilute meshes.

Current opinion in structural biology·2026
Same journal

Tuning the physicochemical properties of rationally designed protein-based biomolecular condensates.

Current opinion in structural biology·2026
See all related articles

Related Experiment Video

Updated: May 3, 2026

Isolation and Characterization of RNA-Containing Exosomes
09:43

Isolation and Characterization of RNA-Containing Exosomes

Published on: January 9, 2012

102.4K

The eukaryotic RNA exosome.

Kurt Januszyk1, Christopher D Lima2

  • 1Structural Biology Program, Sloan-Kettering Institute, 1275 York Avenue, NY, USA.

Current Opinion in Structural Biology
|February 15, 2014
PubMed
Summary
This summary is machine-generated.

The eukaryotic RNA exosome complex, essential for RNA processing, utilizes its core structure to recruit and modulate the activity of key enzymes like Rrp44 and Rrp6 for RNA degradation.

More Related Videos

An Oligonucleotide-based Tandem RNA Isolation Procedure to Recover Eukaryotic mRNA-Protein Complexes
09:45

An Oligonucleotide-based Tandem RNA Isolation Procedure to Recover Eukaryotic mRNA-Protein Complexes

Published on: August 18, 2018

13.1K
Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC
09:15

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC

Published on: May 9, 2020

6.1K

Related Experiment Videos

Last Updated: May 3, 2026

Isolation and Characterization of RNA-Containing Exosomes
09:43

Isolation and Characterization of RNA-Containing Exosomes

Published on: January 9, 2012

102.4K
An Oligonucleotide-based Tandem RNA Isolation Procedure to Recover Eukaryotic mRNA-Protein Complexes
09:45

An Oligonucleotide-based Tandem RNA Isolation Procedure to Recover Eukaryotic mRNA-Protein Complexes

Published on: August 18, 2018

13.1K
Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC
09:15

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC

Published on: May 9, 2020

6.1K

Area of Science:

  • Molecular Biology
  • Biochemistry
  • Cell Biology

Background:

  • The eukaryotic RNA exosome is a crucial multi-subunit ribonuclease complex involved in RNA degradation and processing.
  • Its nine-subunit core shares similarities with bacterial PNPase but lacks intrinsic ribonuclease activity.
  • The exosome core collaborates with Rrp44 (an endo- and exoribonuclease) and Rrp6 (a distributive exoribonuclease).

Purpose of the Study:

  • To elucidate the functional role of the eukaryotic RNA exosome core in coordinating its associated RNase activities.
  • To understand how the core facilitates RNA passage and modulates enzyme function.

Main Methods:

  • Biochemical assays
  • Structural studies
  • Enzyme activity analysis

Main Results:

  • The RNA exosome core is essential for recruiting Rrp44 and Rrp6.
  • The central channel of the exosome core accommodates single-stranded RNA.
  • The core structure modulates the catalytic activities of Rrp44 and Rrp6.

Conclusions:

  • The RNA exosome core acts as a scaffold, essential for the recruitment and regulation of its catalytic subunits.
  • This coordination is vital for the exosome's comprehensive role in RNA metabolism within eukaryotic cells.