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CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments
Three distinct promoters control the master regulator of MHC class II expression, CIITA, in a cell type specific manner. Promoter I (pI) CIITA, expressed primarily by dendritic cells and macrophages, expresses a unique isoform that contains a caspase recruitment domain. The activity and function of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366023/ https://www.ncbi.nlm.nih.gov/pubmed/22218223 http://dx.doi.org/10.1038/gene.2011.86 |
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author | Zinzow-Kramer, Wendy M. Long, Alyssa B. Youngblood, Benjamin A. Rosenthal, Kristen M. Butler, Royce Mohammed, Ata-Ur-Rasheed Skountzou, Ioanna Ahmed, Rafi Evavold, Brian D. Boss, Jeremy M. |
author_facet | Zinzow-Kramer, Wendy M. Long, Alyssa B. Youngblood, Benjamin A. Rosenthal, Kristen M. Butler, Royce Mohammed, Ata-Ur-Rasheed Skountzou, Ioanna Ahmed, Rafi Evavold, Brian D. Boss, Jeremy M. |
author_sort | Zinzow-Kramer, Wendy M. |
collection | PubMed |
description | Three distinct promoters control the master regulator of MHC class II expression, CIITA, in a cell type specific manner. Promoter I (pI) CIITA, expressed primarily by dendritic cells and macrophages, expresses a unique isoform that contains a caspase recruitment domain. The activity and function of this isoform is not understood but has been thought to enhance the function of CIITA in antigen presenting cells. To determine if isoform I of CIITA has specific functions, CIITA mutant mice were created in which isoform I was replaced with isoform III sequences. Mice in which pI and the CARD encoding exon were deleted were also created. No defect in the formation of CD4 T cells, the ability to respond to a model antigen, or bacterial or viral challenge was observed in mice lacking CIITA isoform I. Although CIITA and MHC-II expression was decreased in splenic DC, the pI knockout animals expressed CIITA from downstream promoters, suggesting that control of pI activity is mediated by unknown s II distal elements that could act at the pIII, the B cell promoter. Thus, no critical function is linked to the CARD domain of CIITA isoform I with respect to basic immune system development, function and challenge. |
format | Online Article Text |
id | pubmed-3366023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-33660232012-12-01 CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments Zinzow-Kramer, Wendy M. Long, Alyssa B. Youngblood, Benjamin A. Rosenthal, Kristen M. Butler, Royce Mohammed, Ata-Ur-Rasheed Skountzou, Ioanna Ahmed, Rafi Evavold, Brian D. Boss, Jeremy M. Genes Immun Article Three distinct promoters control the master regulator of MHC class II expression, CIITA, in a cell type specific manner. Promoter I (pI) CIITA, expressed primarily by dendritic cells and macrophages, expresses a unique isoform that contains a caspase recruitment domain. The activity and function of this isoform is not understood but has been thought to enhance the function of CIITA in antigen presenting cells. To determine if isoform I of CIITA has specific functions, CIITA mutant mice were created in which isoform I was replaced with isoform III sequences. Mice in which pI and the CARD encoding exon were deleted were also created. No defect in the formation of CD4 T cells, the ability to respond to a model antigen, or bacterial or viral challenge was observed in mice lacking CIITA isoform I. Although CIITA and MHC-II expression was decreased in splenic DC, the pI knockout animals expressed CIITA from downstream promoters, suggesting that control of pI activity is mediated by unknown s II distal elements that could act at the pIII, the B cell promoter. Thus, no critical function is linked to the CARD domain of CIITA isoform I with respect to basic immune system development, function and challenge. 2012-01-05 2012-06 /pmc/articles/PMC3366023/ /pubmed/22218223 http://dx.doi.org/10.1038/gene.2011.86 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Zinzow-Kramer, Wendy M. Long, Alyssa B. Youngblood, Benjamin A. Rosenthal, Kristen M. Butler, Royce Mohammed, Ata-Ur-Rasheed Skountzou, Ioanna Ahmed, Rafi Evavold, Brian D. Boss, Jeremy M. CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments |
title | CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments |
title_full | CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments |
title_fullStr | CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments |
title_full_unstemmed | CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments |
title_short | CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments |
title_sort | ciita promoter i card-deficient mice express functional mhc class ii genes in myeloid and lymphoid compartments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366023/ https://www.ncbi.nlm.nih.gov/pubmed/22218223 http://dx.doi.org/10.1038/gene.2011.86 |
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