Related Experiment Video
Updated: Apr 7, 2026

06:26
Selective Capture of 5-hydroxymethylcytosine from Genomic DNA
Published on: October 5, 2012
12.4K
Grabbing the genome by the NADs.
Timothy D Matheson1, Paul D Kaufman2
1Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, 01605, USA.
Chromosoma
|July 16, 2015
Summary
Nucleolar-associated domains (NADs) are genomic regions near the nucleolus. These domains, rich in repetitive DNA and heterochromatin marks, may play a role in gene silencing.
Area of Science:
- Genomics
- Epigenetics
- Molecular Biology
Background:
- Nucleolar-associated domains (NADs) are genomic regions interacting with the nucleolus.
- NADs are enriched in repetitive elements, inactive X chromosome regions, and RNA polymerase III genes.
- NADs exhibit heterochromatic marks (H3K27me3, H3K9me3, H4K20me3) and are linked to gene silencing.
Purpose of the Study:
- To review recent findings on factors regulating NAD localization.
- To discuss the mechanisms of NAD localization and gene silencing.
- To identify areas for future research on genome organization and the nucleolus.
Main Methods:
- Deep sequencing
- DNA-fluorescence in situ hybridization (FISH)
- Review of published studies on trans-acting factors.
Main Results:
- NADs contain repetitive elements, inactive X chromosome DNA, and RNA Pol III genes.
- NADs are associated with heterochromatin marks and gene silencing.
- Factors like CTCF, CAF-1 p150, nucleolar proteins, and lncRNAs are implicated in NAD localization.
Conclusions:
- NAD localization to the nucleolar periphery may establish or maintain heterochromatic silencing.
- The coordination of trans-acting factors in NAD localization and silencing requires further investigation.
- Understanding genome organization around the nucleolus has significant mechanistic and functional implications.
More Related Videos
Related Concept Videos
DNA Isolation
47.0K
DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
47.0K
Sanger Sequencing
779.2K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
779.2K
Genomic DNA in Eukaryotes
54.2K
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.
54.2K
Genome Annotation and Assembly
22.2K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
22.2K

