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Related Concept Videos

Positive Regulator Molecules01:45

Positive Regulator Molecules

To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
Positive Regulator Molecules02:39

Positive Regulator Molecules

Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
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Yeasts are single-celled organisms, but unlike bacteria, they are eukaryotes (cells with a nucleus). Cell signaling in yeast is similar to signaling in other eukaryotic cells. A ligand, such as a protein or a small molecule released from a yeast cell, attaches to a receptor on the cell surface. The binding stimulates second-messenger kinases to activate or inactivate transcription factors that further regulate gene expression. Many of the yeast intracellular signaling cascades have similar...
Master Transcription Regulators02:23

Master Transcription Regulators

Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
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Cis-regulatory Sequences

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Related Experiment Video

Updated: Jun 18, 2026

Genome-wide Analysis of Histone Modifications Distribution using the Chromatin Immunoprecipitation Sequencing Method in Magnaporthe oryzae
09:25

Genome-wide Analysis of Histone Modifications Distribution using the Chromatin Immunoprecipitation Sequencing Method in Magnaporthe oryzae

Published on: June 2, 2021

The c-MYC NHE III(1): function and regulation.

Verónica González1, Laurence H Hurley

  • 1University of Arizona, Tucson, 85721, USA.

Annual Review of Pharmacology and Toxicology
|November 20, 2009
PubMed
Summary

The c-MYC gene’s G-quadruplex structure in the NHE III(1) region represses its transcription. Factors modulating this structure and G-quadruplex-inducing drugs offer potential cancer treatments.

Area of Science:

  • Molecular Biology
  • Cancer Biology
  • Drug Discovery

Background:

  • c-MYC is crucial for cell growth and differentiation; its dysregulation is a hallmark of cancer.
  • The nuclease hypersensitive element (NHE) III(1) region of the c-MYC promoter is key for regulating c-MYC expression.
  • G-quadruplex formation in this region is implicated in repressing c-MYC transcription.

Purpose of the Study:

  • To review the formation of G-quadruplex structures in the c-MYC promoter's NHE III(1) region.
  • To discuss factors that influence G-quadruplex formation.
  • To explore small molecules that stabilize G-quadruplexes as potential anticancer agents.

Main Methods:

  • Literature review focusing on G-quadruplex formation in the c-MYC promoter.
  • Analysis of factors modulating G-quadruplex stability.

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  • Discussion of therapeutic strategies involving G-quadruplex stabilization.
  • Main Results:

    • G-quadruplex formation in the c-MYC NHE III(1) region is a significant mechanism for transcriptional repression.
    • Various cellular factors and small molecules can modulate G-quadruplex formation.
    • Stabilizing these structures presents a promising avenue for anticancer drug development.

    Conclusions:

    • Understanding c-MYC G-quadruplex formation is vital for cancer biology and drug development.
    • Targeting c-MYC G-quadruplexes offers a potential therapeutic strategy against various cancers.
    • Further research into G-quadruplex modulators could yield novel anticancer agents.