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Related Concept Videos

Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
Nucleosome Remodeling02:54

Nucleosome Remodeling

Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
The Nucleosome01:19

The Nucleosome

Human DNA is almost two meters long. However, it is compressed inside a tiny nucleus measuring only a few microns in diameter. To make this degree of compaction possible, DNA is organized into several sequential levels so that it can fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
In a chromosome, DNA is wound twice around a protein complex called a histone octamer core, which consists of 8 histone proteins. This...
The Nucleosome02:33

The Nucleosome

DNA in a human cell is almost 2m long and it is packed inside a tiny nucleus that is only a few microns in diameter. The level of compaction of DNA inside the nucleus is astonishing. It is organized into several sequentially higher levels of compaction to fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
DNA is wound twice around a protein complex called histone core, that consist of 8 histone proteins. This complex...
DNA Helicases00:55

DNA Helicases

DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
Replication in Eukaryotes01:29

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
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Related Experiment Video

Updated: Jun 18, 2026

In Situ Nucleosome Assembly for Single-Molecule Correlative Force and Fluorescence Microscopy
05:58

In Situ Nucleosome Assembly for Single-Molecule Correlative Force and Fluorescence Microscopy

Published on: September 6, 2024

Sequence-dependent DNA helical rise and nucleosome stability.

Francesco Pedone1, Daniele Santoni

  • 1Dept. of Genetics and Molecular Biology, Sapienza University, P.A. Moro 3, 00161 Rome, Italy. francesco.pedone@uniroma1.it

BMC Molecular Biology
|December 1, 2009
PubMed
Summary

Nucleosome stability is linked to the symmetric distribution of charges along DNA. Greater symmetry in DNA helical steps correlates with more stable nucleosomes, impacting gene regulation.

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Last Updated: Jun 18, 2026

In Situ Nucleosome Assembly for Single-Molecule Correlative Force and Fluorescence Microscopy
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Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA
10:40

Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA

Published on: September 10, 2013

Area of Science:

  • Molecular Biology
  • Genetics
  • Biophysics

Background:

  • Nucleosomes are fundamental to eukaryotic chromatin structure and gene expression regulation.
  • The nucleosome particle exhibits a symmetric distribution of positive charges on its histone surface, interacting with DNA's negative phosphate backbone.

Purpose of the Study:

  • To investigate the relationship between DNA sequence symmetry and nucleosome stability.
  • To identify DNA sequence features that dictate nucleosome positioning and stability.

Main Methods:

  • Analysis of helical DNA steps in known nucleosomal sequences.
  • Comparison of distances around the nucleosomal dyad axis in synthetic DNA sequences.
  • Evaluation of symmetry patterns in DNA sequences from promoters and known nucleosome positions.

Main Results:

  • A significant correlation exists between the symmetric distribution of helical steps and nucleosome stability.
  • Increased symmetry in DNA distances around the dyad axis leads to more stable nucleosomes.
  • Palinstases, identified by symmetric distribution curves, indicate preferential nucleosome dyad positioning sites.

Conclusions:

  • Nucleosome stability is directly influenced by the symmetry of DNA sequences.
  • Palinstases provide insights into preferred nucleosome positioning.
  • Nucleosomes play a significant role in transcription termination, showing high affinity at termination sites.