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

Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Experimental RNAi02:15

Experimental RNAi

RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
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...

You might also read

Related Articles

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

Sort by
Same author

Single cell heterogeneity and evolution of breast cancer bone metastasis and organoids reveals therapeutic targets for precision medicine.

Annals of oncology : official journal of the European Society for Medical Oncology·2022
Same author

Point Absorber Limits to Future Gravitational-Wave Detectors.

Physical review letters·2021
Same author

Modeling circulating cavity fields using the discrete linear canonical transform.

Journal of the Optical Society of America. A, Optics, image science, and vision·2021
Same author

Constraints on Cosmic Strings Using Data from the Third Advanced LIGO-Virgo Observing Run.

Physical review letters·2021
Same author

Approaching the motional ground state of a 10-kg object.

Science (New York, N.Y.)·2021
Same author

Mode matching error signals using radio-frequency beam shape modulation.

Applied optics·2020

Related Experiment Video

Updated: Jul 1, 2026

Characterization of In Vitro Differentiation of Human Primary Keratinocytes by RNA-Seq Analysis
07:29

Characterization of In Vitro Differentiation of Human Primary Keratinocytes by RNA-Seq Analysis

Published on: May 16, 2020

Differential 5S RNA gene expression in vitro.

A P Wolffe1, D D Brown

  • 1Department of Embryology, Carnegie Institution of Washington, Baltimore, Maryland 21210.

Cell
|December 4, 1987
PubMed
Summary

Transcription factor IIIA (TFIIIA) concentration dictates 5S RNA gene transcription in Xenopus egg extracts. Lowering TFIIIA levels enhances somatic 5S RNA gene transcription over oocyte genes, revealing differential gene regulation mechanisms.

Area of Science:

  • Developmental Biology
  • Molecular Genetics
  • Gene Regulation

Background:

  • Oocyte and somatic 5S RNA gene transcription complexes in Xenopus exhibit differential stability in activated egg extracts.
  • Transcription factor IIIA (TFIIIA) is a key regulator in 5S RNA gene transcription.

Purpose of the Study:

  • To investigate the differential stability of oocyte and somatic 5S RNA gene transcription complexes in Xenopus egg extracts.
  • To determine the role of trans-acting factors, particularly TFIIIA, in regulating 5S RNA gene transcription.

Main Methods:

  • Utilizing extracts from activated Xenopus eggs.
  • Manipulating the concentration of TFIIIA in the egg extracts.
  • Comparing the transcription efficiency of cloned somatic and oocyte 5S RNA genes.

More Related Videos

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
10:34

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells

Published on: December 9, 2022

Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster
04:59

Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster

Published on: March 28, 2025

Related Experiment Videos

Last Updated: Jul 1, 2026

Characterization of In Vitro Differentiation of Human Primary Keratinocytes by RNA-Seq Analysis
07:29

Characterization of In Vitro Differentiation of Human Primary Keratinocytes by RNA-Seq Analysis

Published on: May 16, 2020

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
10:34

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells

Published on: December 9, 2022

Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster
04:59

Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster

Published on: March 28, 2025

Main Results:

  • Oocyte 5S RNA gene transcription complexes are destabilized in activated egg extracts, unlike somatic complexes.
  • Trans-acting factors in destabilized complexes exist in equilibrium with free factors, making transcription concentration-dependent.
  • Reducing TFIIIA levels in egg extracts resulted in up to 400-fold increased transcription of cloned somatic 5S RNA genes compared to oocyte genes.

Conclusions:

  • TFIIIA concentration is a critical limiting factor for 5S RNA gene transcription in Xenopus egg extracts.
  • Differential regulation of oocyte and somatic 5S RNA genes is influenced by TFIIIA availability and complex stability.