DefinitionThis section has been translated automatically.
The myxovirus resistance protein (Mx protein, MxA in humans) is an antiviral protein that plays a central role in the innate immune response - specifically in response to interferon stimulation. It is encoded by the MX1 gene (MX1 stands for: MX Dynamin Like GTPase 1) located on chromosome 21q22.3. Alternative splicing leads to several transcript variants. There is a related gene located next to this gene on chromosome 21. There are also several pseudogenes located in a cluster on chromosome 4. MxA is considered a marker for interferon activity, e.g. in viral infections or autoimmune diseases such as SLE. In diagnostic tests, MxA expression is used as an indicator of viral infection (e.g. to distinguish viral infections from bacterial infections).
General informationThis section has been translated automatically.
General properties:
- Name: Myxovirus resistance protein A (MxA in humans, Mx1/Mx2 in mice)
- Gene: encoded by interferon-stimulated genes (ISGs)
- Induction: MxA is induced by type I interferons (especially IFN-alpha and IFN-beta)
- Localization: MxA is found in the cytoplasm; in some species also in the nucleus
Structure:
- GTPase: MxA proteins belong to the dynamin family of GTPases (these hydrolyze GTP)
- MxA proteins have an N-terminal GTPase domain and a C-terminal effector domain
- MxA proteins can form oligomers (several proteins join together to form a complex)
Function:
The interferon-induced "dynamin-like GTPase" (myxoma resistance protein 1) exhibits antiviral activity against a variety of RNA viruses and some DNA viruses. The target viruses include negative-stranded RNA viruses and HBV by binding and inactivating their ribonucleocapsid. The enzyme can also antagonize the replication of Reoviridae and Asfarviridae. The enzyme inhibits the replication of Thogoto virus (THOV) by preventing the nuclear incorporation of viral nucleocapsids; inhibits the replication of La Crosse virus (LACV) by binding the viral nucleoprotein into perinuclear complexes, thus preventing genome amplification, budding and egress; inhibits influenza A virus (IAV) replication by reducing or delaying NP synthesis and blocking endocytic trafficking of incoming virus particles.
- Other viruses against which MxA is effective:
- Thogotoviruses, Bunyaviruses, SARS-CoV-2 (partially inhibitory)
LiteratureThis section has been translated automatically.
- Caielli S et al. (2024) Type I IFN drives unconventional IL-1β secretion in lupus monocytes. Immunity 57:2497-2513.e12.
- Dorfleutner A et al. (2024) Mx1-ing it up-Mitochondrial relay for interferon-dependent, unconventional IL-1β release in SLE monocytes. Immunity 57:2483-2486
- Fairhurst AM et al. (2009) Type I interferons produced by resident renal cells may promote end-organ disease in autoantibody-mediated glomerulonephritis. J Immunol 183:6831-6838.
- Krustev E et al. (2025) Anti-myxovirus resistance protein 1: a novel biomarker for autoimmune myositis and interstitial lung disease in systemic lupus erythematosus. Ann Rheum Dis S0003-4967: 00177-3.
- Lambers WM et al (2019) Interferon score is increased in incomplete systemic lupus erythematosus and correlates with myxovirus-resistance protein A in blood and skin. Arthritis Res Ther 21:260.
- Liu L et al. (2024) Expression of myxovirus resistance protein A in lupus nephritis and other glomerular nephropathies. J Nephrol 37:2395-2398.
- Zav'yalov VP et al. (2019) Interferon-Inducible Myxovirus Resistance Proteins: Potential Biomarkers for Differentiating Viral from Bacterial Infections. Clin Chem 65:739-750.