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Epigenetic Regulation01:37

Epigenetic Regulation

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Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
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Related Experiment Video

Updated: Apr 30, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
10:31

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice

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[Epigenetics in kidney diseases].

Imari Mimura, Masaomi Nangaku

    Rinsho Byori. the Japanese Journal of Clinical Pathology
    |May 8, 2014
    PubMed
    Summary

    Chronic hypoxia drives kidney disease by altering gene expression. Hypoxia inducible factor 1 (HIF1) epigenetically regulates glucose transporter 3 (GLUT3) via KDM3A, offering new therapeutic targets for kidney disease.

    Area of Science:

    • Epigenetics
    • Molecular Biology
    • Nephrology

    Context:

    • Chronic hypoxia in the kidney tubulointerstitium is a key driver of irreversible kidney disease.
    • Hypoxia inducible factor (HIF) is a master transcriptional regulator activated under low-oxygen conditions.
    • HIF1 has been implicated in organizing histone-modifying enzymes, suggesting epigenetic roles.

    Purpose:

    • To elucidate the epigenetic mechanisms by which HIF1 regulates gene expression under hypoxia.
    • To perform genome-wide analysis of HIF1-binding sites and identify downstream target genes.
    • To investigate the role of HIF1 and histone demethylases in regulating gene expression in chronic hypoxia.

    Summary:

    • Genome-wide analysis (ChIP-seq) revealed HIF1 binds to promoter and enhancer regions.

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  • HIF1 epigenetically regulates SLC2A3 (GLUT3) expression via KDM3A (lysine specific demethylase 3A) under hypoxia.
  • KDM3A is recruited in an HIF1-dependent manner to demethylate H3K9me2 at the SLC2A3 locus, up-regulating its expression.
  • Impact:

    • Identified novel HIF1-dependent epigenetic mechanisms involving KDM3A and chromosomal conformation changes.
    • Demonstrated a direct link between HIF1, KDM3A, and SLC2A3 regulation under hypoxia.
    • Highlights the importance of understanding epigenetic regulation in chronic hypoxia for developing novel therapeutic strategies against chronic kidney disease.