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Related Concept Videos

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The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
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The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
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Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
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Related Experiment Video

Updated: Apr 12, 2026

Live-Cell Imaging of Transcriptional Activity at DNA Double-Strand Breaks
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Regulating transcription traffic around DSBs.

Brian S Plosky1

  • 1Molecular Cell, Cell Press, 600 Technology Square, 5(th) Floor, Cambridge, MA 02139, USA.

Molecular Cell
|May 11, 2015
PubMed
Summary

DNA double-strand breaks (DSBs) trigger mechanisms to halt transcription. Ui et al. reveal a link between elongation factors and repressive complexes to safeguard DNA integrity during repair.

Area of Science:

  • Molecular biology
  • Genetics
  • Cellular mechanisms

Background:

  • DNA double-strand breaks (DSBs) are severe DNA lesions.
  • Transcription can interfere with DNA repair processes.
  • Maintaining genomic stability is crucial for cell survival.

Purpose of the Study:

  • To investigate how cells prevent transcription near DSBs.
  • To identify factors involved in repressing transcription during DNA repair.

Main Methods:

  • The study likely involved molecular biology techniques.
  • Investigated protein-protein interactions.
  • Assessed the impact of DSBs on transcription.

Main Results:

  • A connection was found between an elongation factor and a repressive complex.

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  • This complex prevents RNA polymerase activity near DSBs.
  • Conclusions:

    • Cells possess mechanisms to suppress transcription at DSB sites.
    • This suppression is vital for efficient and accurate DNA repair.