Compendium of Immune Signatures Identifies Conserved and Species-Specific Biology in Response to Inflammation

Gene-expression profiling has become a mainstay in immunology, but subtle changes in gene networks related to biological processes are hard to discern when comparing various datasets. For instance, conservation of the transcriptional response to sepsis in mouse models and human disease remains contr...

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Vydáno v:Immunity (Cambridge, Mass.) Ročník 44; číslo 1; s. 194 - 206
Hlavní autoři: Godec, Jernej, Tan, Yan, Liberzon, Arthur, Tamayo, Pablo, Bhattacharya, Sanchita, Butte, Atul J, Mesirov, Jill P, Haining, W Nicholas
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 19.01.2016
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ISSN:1097-4180
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Abstract Gene-expression profiling has become a mainstay in immunology, but subtle changes in gene networks related to biological processes are hard to discern when comparing various datasets. For instance, conservation of the transcriptional response to sepsis in mouse models and human disease remains controversial. To improve transcriptional analysis in immunology, we created ImmuneSigDB: a manually annotated compendium of ∼5,000 gene-sets from diverse cell states, experimental manipulations, and genetic perturbations in immunology. Analysis using ImmuneSigDB identified signatures induced in activated myeloid cells and differentiating lymphocytes that were highly conserved between humans and mice. Sepsis triggered conserved patterns of gene expression in humans and mouse models. However, we also identified species-specific biological processes in the sepsis transcriptional response: although both species upregulated phagocytosis-related genes, a mitosis signature was specific to humans. ImmuneSigDB enables granular analysis of transcriptomic data to improve biological understanding of immune processes of the human and mouse immune systems.
AbstractList Gene-expression profiling has become a mainstay in immunology, but subtle changes in gene networks related to biological processes are hard to discern when comparing various datasets. For instance, conservation of the transcriptional response to sepsis in mouse models and human disease remains controversial. To improve transcriptional analysis in immunology, we created ImmuneSigDB: a manually annotated compendium of ∼5,000 gene-sets from diverse cell states, experimental manipulations, and genetic perturbations in immunology. Analysis using ImmuneSigDB identified signatures induced in activated myeloid cells and differentiating lymphocytes that were highly conserved between humans and mice. Sepsis triggered conserved patterns of gene expression in humans and mouse models. However, we also identified species-specific biological processes in the sepsis transcriptional response: although both species upregulated phagocytosis-related genes, a mitosis signature was specific to humans. ImmuneSigDB enables granular analysis of transcriptomic data to improve biological understanding of immune processes of the human and mouse immune systems.
Author Godec, Jernej
Tan, Yan
Mesirov, Jill P
Bhattacharya, Sanchita
Butte, Atul J
Tamayo, Pablo
Haining, W Nicholas
Liberzon, Arthur
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  organization: Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA; Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA
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  surname: Tan
  fullname: Tan, Yan
  organization: Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Bioinformatics Program, Boston University, Boston, MA 02215, USA
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  surname: Liberzon
  fullname: Liberzon, Arthur
  organization: Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA
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  fullname: Tamayo, Pablo
  organization: Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA
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  surname: Bhattacharya
  fullname: Bhattacharya, Sanchita
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  surname: Haining
  fullname: Haining, W Nicholas
  email: nicholas_haining@dfci.harvard.edu
  organization: Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Division of Hematology/Oncology, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA. Electronic address: nicholas_haining@dfci.harvard.edu
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Snippet Gene-expression profiling has become a mainstay in immunology, but subtle changes in gene networks related to biological processes are hard to discern when...
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SubjectTerms Animals
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Title Compendium of Immune Signatures Identifies Conserved and Species-Specific Biology in Response to Inflammation
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