Abstract
Activation-induced cytidine deaminase (AID) is specifically expressed in the germinal centers of lymphoid organs, where it initiates targeted hypermutation of variable regions of immunoglobulin genes in response to stimulation by antigen. Ectopic expression of AID, however, mediates generalized hypermutation in eukaryotes and prokaryotes. Here, we present evidence that AID is induced outside the germinal center in response to infection by the Abelson murine leukemia virus. The genotoxic activity of virally induced AID resulted in checkpoint kinase-1 (chk1) phosphorylation and ultimately restricted the proliferation of the infected cell. At the same time, it induced NKG2D ligand upregulation, which alerts the immune system to the presence of virally transformed cells. Hence, in addition to its known function in immunoglobulin diversification, AID is active in innate defense against a transforming retrovirus.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Abelson murine leukemia virus / immunology*
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Animals
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B-Lymphocytes / enzymology
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Bone Marrow / enzymology
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Bone Marrow / virology
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Checkpoint Kinase 1
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Cytidine Deaminase / genetics
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Cytidine Deaminase / physiology*
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Death
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Leukemia, Experimental / enzymology*
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Leukemia, Experimental / genetics
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Leukemia, Experimental / immunology
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Ligands
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Mice
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Mice, Inbred Strains
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NK Cell Lectin-Like Receptor Subfamily K
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Phosphorylation
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Protein Kinases / metabolism
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Receptors, Immunologic / metabolism
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Receptors, Natural Killer Cell
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Retroviridae Infections / enzymology*
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Retroviridae Infections / genetics
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Retroviridae Infections / immunology
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Tumor Virus Infections / enzymology*
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Tumor Virus Infections / genetics
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Tumor Virus Infections / immunology
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Up-Regulation
Substances
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Klrk1 protein, mouse
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Ligands
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NK Cell Lectin-Like Receptor Subfamily K
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Receptors, Immunologic
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Receptors, Natural Killer Cell
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Protein Kinases
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Checkpoint Kinase 1
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Chek1 protein, mouse
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AICDA (activation-induced cytidine deaminase)
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Cytidine Deaminase