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

Ribosome Profiling02:24

Ribosome Profiling

3.2K
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...
3.2K
Modern Molecular Taxonomy01:29

Modern Molecular Taxonomy

865
Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
865
Genomic DNA in Prokaryotes00:46

Genomic DNA in Prokaryotes

42.5K
The genome of most prokaryotic organisms consists of double-stranded DNA organized into one circular chromosome in a region of cytoplasm called the nucleoid. The chromosome is tightly wound, or supercoiled, for efficient storage. Prokaryotes also contain other circular pieces of DNA called plasmids. These plasmids are smaller than the chromosome and often carry genes that confer adaptive functions, such as antibiotic resistance.
Genomic Diversity in Bacteria
Although bacterial genomes are much...
42.5K
Genomic DNA in Eukaryotes00:58

Genomic DNA in Eukaryotes

46.0K
Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
46.0K
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

9.5K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
9.5K
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

12.3K
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,...
12.3K

You might also read

Related Articles

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

Sort by
Same author

Structure and variation in ribosomal RNA genes of pea : Characterization of a cloned rDNA repeat and chromosomal rDNA variants.

Plant molecular biology·2013
Same author

Homologies between nuclear and plastid DNA in spinach.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013
Same author

Structure of melon rDNA and nucleotide sequence of the 17-25S spacer region.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013
Same author

Deletion mutation as a means of isolating avirulence genes in flax rust.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013
Same author

Tobacco nuclear DNA contains long tracts of homology to chloroplast DNA.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013
Same author

Cytoplasmic male sterility (CMS) in Lolium perenne L.: 1. Development of a diagnostic probe for the male-sterile cytoplasm.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013

Related Experiment Video

Updated: May 5, 2026

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

1.2K

Heterogeneity in cucumber ribosomal DNA.

T A Kavanagh1, J N Timmis

  • 1Department of Botany, University College, 4, Belfield, Dublin, Ireland.

TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|November 20, 2013
PubMed
Summary

Cucumber ribosomal DNA (rDNA) repeat units show significant length and sequence heterogeneity. This variation is primarily due to differences in the external spacer region and restriction fragment length polymorphism.

Area of Science:

  • Molecular Biology
  • Genetics
  • Plant Science

Background:

  • Ribosomal DNA (rDNA) comprises repeating units encoding ribosomal RNA (rRNA).
  • Understanding rDNA organization and heterogeneity is crucial for comprehending genome evolution and gene expression in plants.

Purpose of the Study:

  • To characterize the heterogeneity of cucumber ribosomal DNA (rDNA) repeat units.
  • To identify the sources of variation in length and sequence within cucumber rDNA.

Main Methods:

  • Purification of native rDNA using actinomycin-D/CsCl gradients.
  • Cloning of full-length rDNA repeat units.
  • Restriction enzyme digestion and analysis (EcoR I, Xba I, BamH I).
  • R-loop mapping using electron microscopy.

More Related Videos

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
13:16

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA

Published on: January 22, 2018

23.3K
RIBO-seq in Bacteria: a Sample Collection and Library Preparation Protocol for NGS Sequencing
12:05

RIBO-seq in Bacteria: a Sample Collection and Library Preparation Protocol for NGS Sequencing

Published on: August 7, 2021

8.1K

Related Experiment Videos

Last Updated: May 5, 2026

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

1.2K
Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
13:16

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA

Published on: January 22, 2018

23.3K
RIBO-seq in Bacteria: a Sample Collection and Library Preparation Protocol for NGS Sequencing
12:05

RIBO-seq in Bacteria: a Sample Collection and Library Preparation Protocol for NGS Sequencing

Published on: August 7, 2021

8.1K
  • Hybridization with pure 18S and 25S ribosomal RNAs (rRNAs).
  • Main Results:

    • Cucumber rDNA repeat units are heterogeneous in both length and sequence.
    • Five cloned rDNA repeat units represent all EcoR I and Xba I fragments in native DNA.
    • Base modification explains the absence of a BamH I site in some native rDNA.
    • Major heterogeneity stems from variations in the external spacer region length.
    • Restriction fragment length polymorphism was observed in EcoR I digestion.
    • The coding regions for 18S and 25S rRNA are uninterrupted and conserved.

    Conclusions:

    • Cucumber rDNA exhibits significant structural heterogeneity, mainly in the external spacer.
    • Base modification can influence restriction site presence in rDNA.
    • The conserved nature of rRNA coding regions suggests functional importance.