Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Dec;34(12):602-9.
doi: 10.1016/j.it.2013.03.004. Epub 2013 Apr 27.

Immunological Genome Project and systems immunology

Affiliations
Review

Immunological Genome Project and systems immunology

Tal Shay et al. Trends Immunol. 2013 Dec.

Abstract

Immunological studies of single proteins in a single cell type have been complemented in recent years by larger studies, enabled by emerging high-throughput technologies. This trend has recently been exemplified by the discovery of gene networks controlling regulatory and effector αβ T cell subset development and human hematopoiesis. The Immunological Genome Project (ImmGen) aims to decipher the gene networks underpinning mouse hematopoiesis. The first phase, completed in 2012, profiled the transcriptome of 249 immune cell types. We discuss the utilities of the datasets in high-resolution mapping of the hematopoietic system. The immune transcriptome compendium has revealed unsuspected cell lineage relations and the network reconstruction has identified novel regulatory factors of hematopoiesis.

Keywords: hematopoiesis; systems immunology; transcriptional regulation.

PubMed Disclaimer

Figures

Figure 1
Figure 1. The ImmGen compendium and its analysis
(a) ImmGen dataset (top, left), and the three types of studies performed by the ImmGen consortium: (1) Lineage focused studies that identified lineage specific genes (e.g. heatmaps of gene expression across cell subsets), described the relationship between lineages (represented by Pearson correlation matrix) and assigned cell types to the lineages tree. (2) System studies that defined modules of coexpressed genes across the entire dataset and reconstructed the modules’ regulatory program using Ontogenet. The resulting regulatory network described organizational principles governing the differentiation within the immune system, and identified candidate novel regulatory factors that can be experimentally verified. (3) Perturbations studies that investigated the transcriptional response to pathogens. ImmGen dataset can be integrated with other datasets, and methods from other disciplines can be applied to it, to gain new biological perspectives (Future studies). (b) The hematopoietic lineage tree constructed by ImmGen. Big rectangles with numbers represent a group of cell types, with the number of replicates listed. Small rectangles represent single cell type, typically with 3 replicates. Lines/edges between rectangles represent differentiation steps.
Figure 2
Figure 2. Lymphoid and myeloid specific modules and activators
Conserved pan-regulators of lymphoid and myeloid branches can be gleaned from the comparison of lymphoid and myeloid-specific modules. (a) Expression matrix of the genes in the modules that are induced in myeloid cells (Coarse modules 24, 25, 28, 29, 30, 31, 32, 45, 49, 74, 75 and 77). (b) Expression matrix of the activators assigned to the modules that are induced in myeloid cells with a maximal activity weight > 0.05 (arbitrary threshold). (c) Expression matrix of the genes in the modules that are induced in lymphoid cells (Coarse modules 16, 21 and 22). (d) Expression matrix of the activators assigned to the modules that are induced in lymphoid cells with a maximal activity weight > 0.5. Blue-red color bars show relative expression level
Text Box 1 Figure
Text Box 1 Figure. Examples of ImmGen application for gene(s) focused studies
(a) Bar chart of the immune cell type(s) in which a Pax5 is expressed, using the Skyline viewer. (b) A heatmap of the gene expression of the genes in coarse-grained module C33. Each row is a gene, each column is a cell type. Colorbar below represents cell lineage. (c) Heatmap of coarse-grained modules predicted to be controlled by Pax5. Each row is a gene, each column is a cell type. Colorbar below represents cell lineage. (d) B-cells induce modules. Each row is a gene, each column is a cell type. Colorbar below represents cell lineage. (e) Heatmap of genes down-regulated (top) or up-regulated (bottom) in AIDS-related primary effusion lymphoma samples compared to other tumor subtypes and normal B lymphocytes[44], Fig. e). Only genes assigned to ImmGen modules are shown, sorted by module number. Selected gene symbols are shown to the left.

Similar articles

Cited by

References

    1. Lee Y, et al. Induction and molecular signature of pathogenic TH17 cells. Nat Immunol. 2012;13:991–999. - PMC - PubMed
    1. Ciofani M, et al. A Validated Regulatory Network for Th17 Cell Specification. Cell. 2012;151:289–303. - PMC - PubMed
    1. Amit I, et al. Unbiased reconstruction of a mammalian transcriptional network mediating pathogen responses. Science. 2009;326:257–263. - PMC - PubMed
    1. Mullen Alan C, et al. Master Transcription Factors Determine Cell-Type-Specific Responses to TGF-β Signaling. Cell. 2011;147:565–576. - PMC - PubMed
    1. Glasmacher E, et al. A Genomic Regulatory Element That Directs Assembly and Function of Immune-Specific AP-1–IRF Complexes. Science. 2012;338:975–980. - PMC - PubMed

Publication types

LinkOut - more resources