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Scientific article
Open access
English

Identification of CIITA regulated genetic module dedicated for antigen presentation

Published inPLOS genetics, vol. 4, no. 4, e1000058
Publication date2008
Abstract

The class II trans-activator CIITA is a transcriptional co-activator required for the expression of Major Histocompatibility Complex (MHC) genes. Although the latter function is well established, the global target-gene specificity of CIITA had not been defined. We therefore generated a comprehensive list of its target genes by performing genome-wide scans employing four different approaches designed to identify promoters that are occupied by CIITA in two key antigen presenting cells, B cells and dendritic cells. Surprisingly, in addition to MHC genes, only nine new targets were identified and validated by extensive functional and expression analysis. Seven of these genes are known or likely to function in processes contributing to MHC-mediated antigen presentation. The remaining two are of unknown function. CIITA is thus uniquely dedicated for genes implicated in antigen presentation. The finding that CIITA regulates such a highly focused gene expression module sets it apart from all other transcription factors, for which large-scale binding-site mapping has indicated that they exert pleiotropic functions and regulate large numbers of genes.

Keywords
  • B-Lymphocytes
  • Base Sequence
  • Binding Sites
  • Cell Line
  • Chromatin Immunoprecipitation
  • DNA
  • DNA-Binding Proteins
  • Dendritic Cells
  • Enhancer Elements (Genetics)
  • Genes
  • MHC Class II
  • Humans
  • Interferon-gamma Recombinant
  • Nuclear Proteins
  • Promoter Regions (Genetics)
  • Trans-Activation (Genetics)
  • Trans-Activators
  • Transcription Factors
Citation (ISO format)
KRAWCZYK, Michal et al. Identification of CIITA regulated genetic module dedicated for antigen presentation. In: PLOS genetics, 2008, vol. 4, n° 4, p. e1000058. doi: 10.1371/journal.pgen.1000058
Main files (1)
Article (Accepted version)
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Identifiers
ISSN of the journal1553-7390
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Technical informations

Creation12/08/2008 2:00:00 PM
First validation12/08/2008 2:00:00 PM
Update time03/14/2023 2:59:30 PM
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