Medical Journals

Xbp1 Controls Diverse Cell Type- and Condition-specific Transcriptional Regulatory Networks.

Authors:
  • Acosta-Alvear Diego
  • Zhou Yiming
  • Blais Alexandre
  • Tsikitis Mary
  • Lents Nathan H
  • Arias Carolina
  • Lennon Christen J
  • Kluger Yuval
  • Dynlacht Brian David

From: New York University School of Medicine, New York, NY 10016, USA.

Molecular cell

  • Publish Date: Jul 2007
  • ISSN: 1097-2765
  • Volume: 27
  • Issue: 1
  • Pages: 53-66
  • Medium: Print
  • Language: English
  • Citation (JAMA): Acosta-Alvear Diego, Zhou Yiming, Blais Alexandre, et al. Xbp1 Controls Diverse Cell Type- and Condition-specific Transcriptional Regulatory Networks.. Mol. Cell Jul 2007;27:53-66

Abstract

Using genome-wide approaches, we have elucidated the regulatory circuitry governed by the XBP1 transcription factor, a key effector of the mammalian unfolded protein response (UPR), in skeletal muscle and secretory cells. We identified a core group of genes involved in constitutive maintenance of ER function in all cell types and tissue- and condition-specific targets. In addition, we identified a cadre of unexpected targets that link XBP1 to neurodegenerative and myodegenerative diseases, as well as to DNA damage and repair pathways. Remarkably, we found that XBP1 regulates functionally distinct targets through different sequence motifs. Further, we identified Mist1, a critical regulator of differentiation, as an important target of XBP1, providing an explanation for developmental defects associated with XBP1 loss of function. Our results provide a detailed picture of the regulatory roadmap governed by XBP1 in distinct cell types as well as insight into unexplored functions of XBP1.

Mesh Headings (Keywords): Animals, Base Sequence, Basic Helix-Loop-Helix Transcription Factors, Binding Sites, Chromatin Immunoprecipitation, Computational Biology, DNA-Binding Proteins, Endoplasmic Reticulum, Energy Metabolism, Gene Expression Regulation, Gene Regulatory Networks, Genome, Mice, Molecular Sequence Data, Muscle Development, Muscle, Skeletal, Muscular Diseases, Neurodegenerative Diseases, Nuclear Proteins, Protein Binding, Protein Folding, Rats, Reproducibility of Results, Substrate Specificity


Check for Full Text / PubMed Unique Identifier (PMID): 17612490


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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