EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming
T box transcription factor Eomesodermin (EOMES) is induced when naïve T cells are converted to innate memory T cells in response to cytokines. Here the authors show that EOMES is recruited to RUNX3-bound enhancers and interacts with BRG1 during innate memory T cell formation.
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2019-07-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-019-11233-6 |
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doaj-977399acbe71487ca1c96fd6df9b20922021-05-11T11:49:56ZengNature Publishing GroupNature Communications2041-17232019-07-0110111710.1038/s41467-019-11233-6EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogrammingNicolas Istaces0Marion Splittgerber1Viviana Lima Silva2Muriel Nguyen3Séverine Thomas4Aurore Le5Younes Achouri6Emilie Calonne7Matthieu Defrance8François Fuks9Stanislas Goriely10Abdulkader Azouz11Université Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Catholique de Louvain, Institut de DuveUniversité Libre de Bruxelles, Laboratory of Cancer EpigeneticsUniversité Libre de Bruxelles, Interuniversity Institute of Bioinformatics in Brussels (IB2)Université Libre de Bruxelles, Laboratory of Cancer EpigeneticsUniversité Libre de Bruxelles, Institute for Medical Immunology (IMI)Université Libre de Bruxelles, Institute for Medical Immunology (IMI)T box transcription factor Eomesodermin (EOMES) is induced when naïve T cells are converted to innate memory T cells in response to cytokines. Here the authors show that EOMES is recruited to RUNX3-bound enhancers and interacts with BRG1 during innate memory T cell formation.https://doi.org/10.1038/s41467-019-11233-6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nicolas Istaces Marion Splittgerber Viviana Lima Silva Muriel Nguyen Séverine Thomas Aurore Le Younes Achouri Emilie Calonne Matthieu Defrance François Fuks Stanislas Goriely Abdulkader Azouz |
spellingShingle |
Nicolas Istaces Marion Splittgerber Viviana Lima Silva Muriel Nguyen Séverine Thomas Aurore Le Younes Achouri Emilie Calonne Matthieu Defrance François Fuks Stanislas Goriely Abdulkader Azouz EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming Nature Communications |
author_facet |
Nicolas Istaces Marion Splittgerber Viviana Lima Silva Muriel Nguyen Séverine Thomas Aurore Le Younes Achouri Emilie Calonne Matthieu Defrance François Fuks Stanislas Goriely Abdulkader Azouz |
author_sort |
Nicolas Istaces |
title |
EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming |
title_short |
EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming |
title_full |
EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming |
title_fullStr |
EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming |
title_full_unstemmed |
EOMES interacts with RUNX3 and BRG1 to promote innate memory cell formation through epigenetic reprogramming |
title_sort |
eomes interacts with runx3 and brg1 to promote innate memory cell formation through epigenetic reprogramming |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2019-07-01 |
description |
T box transcription factor Eomesodermin (EOMES) is induced when naïve T cells are converted to innate memory T cells in response to cytokines. Here the authors show that EOMES is recruited to RUNX3-bound enhancers and interacts with BRG1 during innate memory T cell formation. |
url |
https://doi.org/10.1038/s41467-019-11233-6 |
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