Transcriptional Regulation of the Human Acid α-Glucosidase Gene

IDENTIFICATION OF A REPRESSOR ELEMENT AND ITS TRANSCRIPTION FACTORS Hes-1 AND YY1*

Abstract

Acid α-glucosidase, the product of a housekeeping gene, is a lysosomal enzyme that degrades glycogen. A deficiency of this enzyme is responsible for a recessively inherited myopathy and cardiomyopathy, glycogenesis type II. We have previously demonstrated that the human acid α-glucosidase gene expression is regulated by a silencer within intron 1, which is located in the 5′-untranslated region. In this study, we have used deletion analysis, electrophoretic mobility shift assay, and footprint analysis to further localize the silencer to a 25-base pair element. The repressive effect on the TK promoter was about 50% in both orientations in expression plasmid, and two transcriptional factors were identified with antibodies binding specifically to the element. Mutagenesis and functional analyses of the element demonstrated that the mammalian homologue 1 of Drosophila hairy andEnhancer of split (Hes-1) binding to an E box (CACGCG) and global transcription factor-YY1 binding to its core site function as a transcriptional repressor. Furthermore, the overexpression of Hes-1 significantly enhanced the repressive effect of the silencer element. The data should be helpful in understanding the expression and regulation of the human acid α-glucosidase gene as well as other lysosomal enzyme genes.

  • Abbreviations:
    GAA
    acid α-glucosidase
    kb
    kilobase(s) or kilobase pair(s)
    bp
    base pair(s)
    YY1
    Ying Yang 1
    Hes-1
    mammalian homologue 1 of D. hairy and Enhancer of split (E(spl))
    TK
    thymidine kinase
    CAT
    chloramphenicol acetyltransferase
    hGH
    human growth hormone
    bHLH
    basic helix-loop-helix
    hASH1
    humanachaete-scute homologue-1
    EMSA
    electrophoretic mobility shift assay
    • Received July 6, 2000.
    • Revision received October 13, 2000.
    Table of Contents

    This Article

    1. The Journal of Biological Chemistry 276, 1789-1793.
    1. All Versions of this Article:
      1. M005959200v1
      2. 276/3/1789 (most recent)

    Article Usage Stats

    Submit your work to JBC.

    You'll be in good company.