Chromatin is the macromolecular state in which nuclear DNA is packaged within the cell. Nucleosomes are the structural units of chromatin. Each nucleosome is composed of ~147 bp double stranded DNA and a histone octamer which contains two copies of each core histone (H2A, H2B, H3 and H4). Histone H1, a linker histone, is involved in binding between nucleosomes to further compact the chromatin. The striking features of these nucleosomal histones are their amino terminus tails which are often modified by various histone modifying enzymes. The predominate modifications on histone tails include but are not limited to methylation, acetylation and phosphorylation. Histone modifications are key to transcription, replication and DNA repair functions (1, 2).
FAQs for Histones & Nucleosome Assembly
Protocols for Histones & Nucleosome Assembly
The Epigenetics brochure provides information on these unique solutions to study DNA and histone modifications. NEB offers a suite of validated products for epigenetics research.
Other Tools & Resources
Follow NEB Product Development Scientist, Romas Vaisvila, Ph.D., as he demonstrates the EpiMark® 5-mc and 5-hmc Analysis Kit for locus specific identification and quantification of 5-hmc in this protocol "High Sensitivity 5-hmc detection in Balb/C Brain Tissue".
If all cells are created from the same genetic material, why are there so many different cell types? Listen to Sriharsa Pradhan, Senior Scientist, RNA Biology at NEB, as he describes how DNA is methylated and how this affects the path of reading the DNA code the same way an obstruction would derail a train off its tracks.