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Related Concept Videos

Chromatin Structure Regulates pre-mRNA Processing02:41

Chromatin Structure Regulates pre-mRNA Processing

In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
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Chromatin Structure and RNA Splicing02:41

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In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
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Chromatin Position Affects Gene Expression02:35

Chromatin Position Affects Gene Expression

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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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 DNA...

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A Multilabel Single Molecule Localization Microscopy Protocol for Investigation of Chromatin in the Dense Nuclear Environment
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Chromatin organization marks exon-intron structure.

Schraga Schwartz1, Eran Meshorer, Gil Ast

  • 1Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel-Aviv University, Ramat Aviv, Israel.

Nature Structural & Molecular Biology
|August 18, 2009
PubMed
Summary
This summary is machine-generated.

Chromatin structure influences gene expression by regulating transcription and splicing. This study reveals increased nucleosome occupancy on exons, impacting exon selection and gene regulation.

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Area of Science:

  • Molecular Biology
  • Genomics
  • Epigenetics

Background:

  • Transcription and splicing are coupled processes.
  • Chromatin organization is known to regulate transcription.
  • The interplay between chromatin structure and exon-intron architecture is largely unexplored.

Purpose of the Study:

  • To investigate the relationship between chromatin structure and exon-intron architecture.
  • To identify how nucleosome positioning and histone modifications correlate with exon and intron regions.
  • To understand the implications for gene regulation, specifically exon selection.

Main Methods:

  • Analysis of genome-wide nucleosome-positioning data in humans, flies, and worms.
  • Examination of genome-wide chromatin immunoprecipitation data in humans and mice.
  • Correlation of histone modification patterns with exon and intron sequences.

Main Results:

  • Exons exhibit higher nucleosome occupancy compared to introns.
  • Differential GC content and nucleosome-disfavoring elements contribute to this pattern.
  • Four specific post-translational histone modifications are enriched in exons, including H3K36me3.
  • Increased nucleosome occupancy along exons is a fundamental phenomenon underlying histone modification enrichment.

Conclusions:

  • Chromatin structure and exon-intron architecture are interconnected.
  • RNA polymerase II mediates cross-talk between chromatin structure and exon-intron architecture.
  • Exon selection may be modulated by chromatin structure, offering new insights into gene regulation.