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Related Concept Videos

The Nucleosome01:19

The Nucleosome

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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...
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Nucleosome Remodeling02:54

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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.
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The Nucleosome Core Particle01:12

The Nucleosome Core Particle

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Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
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Chromatin Packaging01:32

Chromatin Packaging

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Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
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Chromatin Position Affects Gene Expression02:35

Chromatin Position Affects Gene Expression

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Chromatin is the massive complex of DNA and proteins packaged inside the nucleus. The complexity of chromatin folding and how it is packaged inside the nucleus greatly influences  access to genetic information. Generally, the nucleus' periphery is considered transcriptionally repressive, while the cell's interior is considered a transcriptionally active area. 
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DNA Packaging00:58

DNA Packaging

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Author Spotlight: Efficient Nucleosome Reconstitution for Single-Molecule Techniques
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Author Spotlight: Efficient Nucleosome Reconstitution for Single-Molecule Techniques

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Nucleosome positioning based on DNA sequence embedding and deep learning.

Guo-Sheng Han1,2, Qi Li3,4, Ying Li3,5

  • 1Department of Mathematics and Computational Science, Xiangtan University, Xiangtan, 411105, Hunan, China. hangs@xtu.edu.cn.

BMC Genomics
|April 14, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces NP_CBiR, a deep learning model for nucleosome positioning. It achieves high accuracy by integrating convolutional neural networks and bidirectional recurrent neural networks to analyze DNA sequences.

Keywords:
Bidirectional recurrent neural networkConvolutional neural networkDeep learningNucleosome positioningWord vector

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Nucleosome positioning is crucial for understanding DNA regulation.
  • Explosive growth in biological data necessitates efficient algorithms.
  • Existing methods like CNNs capture local features but miss base order.

Purpose of the Study:

  • To develop an efficient nucleosome positioning algorithm.
  • To leverage deep learning for improved DNA sequence analysis.
  • To enhance the prediction performance of nucleosome positioning.

Main Methods:

  • Utilized word vectors for DNA sequence representation.
  • Developed three novel deep learning models for nucleosome positioning.
  • Proposed an integrative model, NP_CBiR, combining CNN and bidirectional RNN.

Main Results:

  • The NP_CBiR model demonstrated superior prediction performance.
  • Achieved high accuracies: 86.18% (H. sapiens), 89.39% (C. elegans), 85.55% (D. melanogaster).
  • Effectively extracted both local and long-term dependent features of DNA sequences.

Conclusions:

  • NP_CBiR effectively extracts local and base order features from DNA.
  • The model's performance highlights the benefit of integrating different network structures.
  • NP_CBiR serves as a valuable complementary tool for nucleosome positioning studies.