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Identification of transcriptional regulators in the mouse immune system

The differentiation of hematopoietic stem cells into immune cells has been extensively studied in mammals, but the transcriptional circuitry controlling it is still only partially understood. Here, the Immunological Genome Project gene expression profiles across mouse immune lineages allowed us to s...

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Detalles Bibliográficos
Autores principales: Jojic, Vladimir, Shay, Tal, Sylvia, Katelyn, Zuk, Or, Sun, Xin, Kang, Joonsoo, Regev, Aviv, Koller, Daphne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690947/
https://www.ncbi.nlm.nih.gov/pubmed/23624555
http://dx.doi.org/10.1038/ni.2587
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author Jojic, Vladimir
Shay, Tal
Sylvia, Katelyn
Zuk, Or
Sun, Xin
Kang, Joonsoo
Regev, Aviv
Koller, Daphne
author_facet Jojic, Vladimir
Shay, Tal
Sylvia, Katelyn
Zuk, Or
Sun, Xin
Kang, Joonsoo
Regev, Aviv
Koller, Daphne
author_sort Jojic, Vladimir
collection PubMed
description The differentiation of hematopoietic stem cells into immune cells has been extensively studied in mammals, but the transcriptional circuitry controlling it is still only partially understood. Here, the Immunological Genome Project gene expression profiles across mouse immune lineages allowed us to systematically analyze these circuits. Using a computational algorithm called Ontogenet, we uncovered differentiation-stage specific regulators of mouse hematopoiesis, identifying many known hematopoietic regulators, and 175 new candidate regulators, their target genes, and the cell types in which they act. Among the novel regulators, we highlight the role of ETV5 in γδT cells differntiation. Since the transcriptional program of human and mouse cells is highly conserved(1), it is likely that many lessons learned from the mouse model apply to humans.
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spelling pubmed-36909472013-12-01 Identification of transcriptional regulators in the mouse immune system Jojic, Vladimir Shay, Tal Sylvia, Katelyn Zuk, Or Sun, Xin Kang, Joonsoo Regev, Aviv Koller, Daphne Nat Immunol Article The differentiation of hematopoietic stem cells into immune cells has been extensively studied in mammals, but the transcriptional circuitry controlling it is still only partially understood. Here, the Immunological Genome Project gene expression profiles across mouse immune lineages allowed us to systematically analyze these circuits. Using a computational algorithm called Ontogenet, we uncovered differentiation-stage specific regulators of mouse hematopoiesis, identifying many known hematopoietic regulators, and 175 new candidate regulators, their target genes, and the cell types in which they act. Among the novel regulators, we highlight the role of ETV5 in γδT cells differntiation. Since the transcriptional program of human and mouse cells is highly conserved(1), it is likely that many lessons learned from the mouse model apply to humans. 2013-04-28 2013-06 /pmc/articles/PMC3690947/ /pubmed/23624555 http://dx.doi.org/10.1038/ni.2587 Text en Users may view, print, copy, download and 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
Jojic, Vladimir
Shay, Tal
Sylvia, Katelyn
Zuk, Or
Sun, Xin
Kang, Joonsoo
Regev, Aviv
Koller, Daphne
Identification of transcriptional regulators in the mouse immune system
title Identification of transcriptional regulators in the mouse immune system
title_full Identification of transcriptional regulators in the mouse immune system
title_fullStr Identification of transcriptional regulators in the mouse immune system
title_full_unstemmed Identification of transcriptional regulators in the mouse immune system
title_short Identification of transcriptional regulators in the mouse immune system
title_sort identification of transcriptional regulators in the mouse immune system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690947/
https://www.ncbi.nlm.nih.gov/pubmed/23624555
http://dx.doi.org/10.1038/ni.2587
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