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Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes

Major histocompatibility complex (MHC)-I and MHC-II molecules play an essential role in the immune response to pathogens by virtue of their ability to present peptides to CD8(+) and CD4(+) T cells, respectively. Given this critical role, MHC-I and MHC-II genes are regulated in a tight fashion at the...

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Autor principal: van den Elsen, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342053/
https://www.ncbi.nlm.nih.gov/pubmed/22566838
http://dx.doi.org/10.3389/fimmu.2011.00048
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author van den Elsen, Peter J.
author_facet van den Elsen, Peter J.
author_sort van den Elsen, Peter J.
collection PubMed
description Major histocompatibility complex (MHC)-I and MHC-II molecules play an essential role in the immune response to pathogens by virtue of their ability to present peptides to CD8(+) and CD4(+) T cells, respectively. Given this critical role, MHC-I and MHC-II genes are regulated in a tight fashion at the transcriptional level by a variety of transcription factors that interact with conserved cis-acting regulatory promoter elements. In addition to the activities of these regulatory factors, modification of chromatin also plays an essential role in the efficient transcription of these genes to meet with local requirement for an effective immune response. The focus of this review is on the transcription factors that interact with conserved cis-acting promoter elements and the epigenetic mechanisms that modulate induced and constitutive expression of these MHC genes.
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spelling pubmed-33420532012-05-07 Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes van den Elsen, Peter J. Front Immunol Immunology Major histocompatibility complex (MHC)-I and MHC-II molecules play an essential role in the immune response to pathogens by virtue of their ability to present peptides to CD8(+) and CD4(+) T cells, respectively. Given this critical role, MHC-I and MHC-II genes are regulated in a tight fashion at the transcriptional level by a variety of transcription factors that interact with conserved cis-acting regulatory promoter elements. In addition to the activities of these regulatory factors, modification of chromatin also plays an essential role in the efficient transcription of these genes to meet with local requirement for an effective immune response. The focus of this review is on the transcription factors that interact with conserved cis-acting promoter elements and the epigenetic mechanisms that modulate induced and constitutive expression of these MHC genes. Frontiers Research Foundation 2011-10-04 /pmc/articles/PMC3342053/ /pubmed/22566838 http://dx.doi.org/10.3389/fimmu.2011.00048 Text en Copyright © 2011 van den Elsen. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Immunology
van den Elsen, Peter J.
Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes
title Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes
title_full Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes
title_fullStr Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes
title_full_unstemmed Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes
title_short Expression Regulation of Major Histocompatibility Complex Class I and Class II Encoding Genes
title_sort expression regulation of major histocompatibility complex class i and class ii encoding genes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342053/
https://www.ncbi.nlm.nih.gov/pubmed/22566838
http://dx.doi.org/10.3389/fimmu.2011.00048
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