Literature DB >> 12065598

The human acid alpha-glucosidase gene is a novel target of the Notch-1/Hes-1 signaling pathway.

Bo Yan1, Nina Raben, Paul Plotz.   

Abstract

Acid alpha-glucosidase (GAA) is a lysosomal enzyme that degrades glycogen. A deficiency of GAA is responsible for a recessively inherited myopathy and cardiomyopathy, glycogenosis type II. Previously, we identified an intronic repressor element in the GAA gene and demonstrated that Hes-1, a basic helix-loop-helix factor, binds to a C class E box within the element and functions as a transcriptional repressor in HepG2 cells. Hes-1 is a well studied downstream target gene in the Notch signaling pathway. In this study, over-expression and depletion of Notch-1 intracellular domain (NICD) strategies were used to investigate whether expression of the GAA gene is under the control of Notch-1/Hes-1 signaling. In co-transfection experiments, Hes-1, up-regulated by over-expressed NICD, enhanced the repressive effect of the DNA element with wild type Hes-1 binding sites but not with mutant Hes-1 binding sites. Conversely, depletion of Notch-1 with phosphorothioated antisense oligonucleotides, corresponding to the fourth ankyrin repeat within NICD, led to reduced Hes-1. Constitutively over-expressed Hes-1 and Notch-1 repressed GAA gene expression. Therefore, our data establish that the human GAA gene, encoding a lysosomal enzyme, is a downstream target of the Notch-1/Hes-1 signaling pathway.

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Year:  2002        PMID: 12065598     DOI: 10.1074/jbc.M204721200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  Atorvastatin promotes presenilin-1 expression and Notch1 activity and increases neural progenitor cell proliferation after stroke.

Authors:  Jieli Chen; Alex Zacharek; Ang Li; Xu Cui; Cynthia Roberts; Mei Lu; Michael Chopp
Journal:  Stroke       Date:  2007-12-06       Impact factor: 7.914

2.  A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations.

Authors:  Andreas Herzog; Ralf Hartung; Arnold J J Reuser; Pia Hermanns; Heiko Runz; Nesrin Karabul; Seyfullah Gökce; Joachim Pohlenz; Christoph Kampmann; Christina Lampe; Michael Beck; Eugen Mengel
Journal:  Orphanet J Rare Dis       Date:  2012-06-07       Impact factor: 4.123

3.  Regulation and role of glycophagy in skeletal muscle energy metabolism.

Authors:  Timothy D Heden; Lisa S Chow; Curtis C Hughey; Douglas G Mashek
Journal:  Autophagy       Date:  2021-09-10       Impact factor: 13.391

4.  Three-dimensional tissue-engineered human skeletal muscle model of Pompe disease.

Authors:  Jason Wang; Chris J Zhou; Alastair Khodabukus; Sabrina Tran; Sang-Oh Han; Aaron L Carlson; Lauran Madden; Priya S Kishnani; Dwight D Koeberl; Nenad Bursac
Journal:  Commun Biol       Date:  2021-05-05

5.  Genotype-phenotype correlation in Pompe disease, a step forward.

Authors:  Paola De Filippi; Kolsoum Saeidi; Sabrina Ravaglia; Andrea Dardis; Corrado Angelini; Tiziana Mongini; Lucia Morandi; Maurizio Moggio; Antonio Di Muzio; Massimiliano Filosto; Bruno Bembi; Fabio Giannini; Giovanni Marrosu; Miriam Rigoldi; Paola Tonin; Serenella Servidei; Gabriele Siciliano; Annalisa Carlucci; Claudia Scotti; Mario Comelli; Antonio Toscano; Cesare Danesino
Journal:  Orphanet J Rare Dis       Date:  2014-08-08       Impact factor: 4.123

  5 in total

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