GeneSet Information

Tier II GS136596 • resistance to thymic deletion 1 (Rthyd1, Published QTL Chr 7)

DESCRIPTION:

QTL associated with resistance to thymic deletion 1. This interval was obtained by using a fixed interval width of 25 Mbp around the peak marker (132776553)

LABEL:

QTL-Rthyd1-Mouse-Chr 7

SCORE TYPE:

Binary

DATE ADDED:

2012-04-02

DATE UPDATED:

2020-05-06

SPECIES:

AUTHORS:

Liston A, Lesage S, Gray DH, O\'Reilly LA, Strasser A, Fahrer AM, Boyd RL, Wilson J, Baxter AG, Gallo EM, Crabtree GR, Peng K, Wilson SR, Goodnow CC

TITLE:

Generalized resistance to thymic deletion in the NOD mouse; a polygenic trait characterized by defective induction of Bim.

JOURNAL:

Immunity Dec 2004, Vol 21, pp. 817-30

ABSTRACT:

The cause of common polygenic autoimmune diseases is not understood because of genetic and cellular complexity. Here, we pinpoint the action of a subset of autoimmune susceptibility loci in the NOD mouse strain linked to D1mit181, D2mit490, D7mit101, and D15mit229, which cause a generalized resistance to thymic deletion in vivo that applies equally to Aire-induced organ-specific gene products in the thymic medulla and to systemic antigens expressed at high levels throughout the thymus and affects CD4(+), CD4(+)8(+), and CD4(+)25(+) thymocytes. Resistance to thymic deletion does not reflect a general deficit in TCR signaling to calcineurin- or ERK-induced genes, imbalance in constitutive regulators of apoptosis, nor excessive signaling to prosurvival genes but is distinguished by failure to induce the proapoptotic gene and protein, Bim, during in vivo encounter with high-avidity autoantigen. These findings establish defects in thymic deletion and Bim induction as a key mechanism in the pathogenesis of autoimmunity. PUBMED: 15589170
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Annotation Information

No sequence read archive data associated with this GeneSet.


Antigens (D000941)
Autoimmune Diseases (D001327)
Multifactorial Inheritance (D020412)
Mice, Inbred NOD (D016688)
Autoimmunity (D015551)
Thymus Gland (D013950)
Apoptosis (D017209)
pathogenesis (GO:0009405)
signaling (GO:0023052)

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