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

Epigenetic Regulation01:37

Epigenetic Regulation

3.2K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
3.2K
General Transcription Factors01:30

General Transcription Factors

5.9K
Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
5.9K
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

6.8K
Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
6.8K
Position-effect Variegation02:32

Position-effect Variegation

6.7K
In 1928, a German botanist Emil Heitz observed the moss nuclei with a DNA binding dye. He observed that while some chromatin regions decondense and spread out in the interphase nucleus, others do not. He termed them euchromatin and heterochromatin, respectively. He proposed that the heterochromatin regions reflect a functionally inactive state of the genome. It was later confirmed that heterochromatin is transcriptionally repressed, and euchromatin is transcriptionally active chromatin.
6.7K
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

35.6K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
35.6K
Histone Modification02:32

Histone Modification

14.7K
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
14.7K

You might also read

Related Articles

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

Sort by
Same author

The challenge and promise of studying human antigen-specific T cells.

Nature reviews. Immunology·2026
Same author

Evaluation of a supermarket placement strategy to nudge healthier dietary habits: synopsis of the WRAPPED study.

Public health research (Southampton, England)·2026
Same author

Rethinking CAR-T manufacturing paradigms: terminology, operational considerations, and economic trade-offs.

Cytotherapy·2026
Same author

Health-related quality of life instruments for older persons with osteoporosis: a WHO-BOHEG systematic review of measurement properties for use in clinical trials and routine practice.

Age and ageing·2026
Same author

Correction: Predictive value of BMD for hip and other fractures: a meta-analysis to update FRAX.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2026
Same author

Cognitive and Executive Function Scores at Age 7 in Relation to Maternal Mid-Pregnancy Plasma Nutrient Mixtures in a Singaporean Family Follow-Up Cohort.

Nutrients·2026

Related Experiment Video

Updated: Oct 22, 2025

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
09:42

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images

Published on: September 7, 2017

9.9K

Human non-CpG methylation patterns display both tissue-specific and inter-individual differences suggestive of

Philip Titcombe1, Robert Murray2, Matthew Hewitt2

  • 1MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.

Epigenetics
|August 31, 2021
PubMed
Summary

Non-CpG DNA methylation shows distinct patterns. CAC methylation is tissue-specific, while CAT methylation reflects individual variations, offering insights into the broader methylome.

Keywords:
CACCATCHGCHHCNNCpGDNA methylationHCAclustercomparisonhierarchical clustering analysishumanindividual-specificmethylationmethylation patternsmusclenon-CpGperipheral bloodtissue-specificumbilical cordumbilical cord blood

More Related Videos

Targeted DNA Methylation Analysis by Next-generation Sequencing
08:38

Targeted DNA Methylation Analysis by Next-generation Sequencing

Published on: February 24, 2015

37.5K
Immunohistochemical Detection of 5-Methylcytosine and 5-Hydroxymethylcytosine in Developing and Postmitotic Mouse Retina
07:50

Immunohistochemical Detection of 5-Methylcytosine and 5-Hydroxymethylcytosine in Developing and Postmitotic Mouse Retina

Published on: August 29, 2018

9.2K

Related Experiment Videos

Last Updated: Oct 22, 2025

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
09:42

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images

Published on: September 7, 2017

9.9K
Targeted DNA Methylation Analysis by Next-generation Sequencing
08:38

Targeted DNA Methylation Analysis by Next-generation Sequencing

Published on: February 24, 2015

37.5K
Immunohistochemical Detection of 5-Methylcytosine and 5-Hydroxymethylcytosine in Developing and Postmitotic Mouse Retina
07:50

Immunohistochemical Detection of 5-Methylcytosine and 5-Hydroxymethylcytosine in Developing and Postmitotic Mouse Retina

Published on: August 29, 2018

9.2K

Area of Science:

  • Epigenetics
  • Genomics

Background:

  • DNA methylation (DNAm) is crucial in mammals, primarily studied at CpG sites.
  • Non-CpG DNAm is prevalent but less understood regarding its functional relevance, tissue distribution, and individual variability.

Purpose of the Study:

  • To investigate non-CpG DNAm across multiple tissues from the same individuals.
  • To understand the distribution of non-CpG DNAm in different tissues and individuals.
  • To correlate non-CpG DNAm with genomic regulatory features.

Main Methods:

  • Methylation sequencing (methyl-seq) of DNA from umbilical cord, cord blood, and peripheral venous blood.
  • Hierarchical cluster analysis (HCA) of CpG and non-CpG sites, stratified by cytosine context (CNN).
  • Analysis of tissue and inter-individual variation in a second dataset including muscle and cord blood samples.

Main Results:

  • Non-CpG methylation clustering patterns differed based on the CNN sequence context.
  • CAC methylation sites showed tissue-specific clustering, followed by individual clustering.
  • CAT methylation sites predominantly clustered by individual, indicating strong personal influence.

Conclusions:

  • CAC DNA methylation exhibits tissue-specific characteristics.
  • CAT DNA methylation is significantly influenced by individual factors, potentially genetic or environmental.
  • This study highlights the complex, context-dependent nature of non-CpG DNA methylation.