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      <dc:title>Immunoproteasome activation enables human TRIM5α restriction of HIV-1</dc:title>
      <dc:creator>Jiménez-Guardeño, José Manuel</dc:creator>
      <dc:creator>Apolonia, Luis</dc:creator>
      <dc:creator>Betancor, Gilberto</dc:creator>
      <dc:creator>Malim, Michael H.</dc:creator>
      <dc:subject>Virología</dc:subject>
      <dc:description>Type 1 interferon suppresses viral replication by upregulating the expression of interferon-stimulated genes with diverse antiviral properties1. The replication of human immunodeficiency virus type 1 (HIV-1) is naturally inhibited by interferon, with the steps between viral entry and chromosomal integration of viral DNA being notably susceptible2-5. The interferon-stimulated gene myxovirus resistance 2 has been defined as an effective postentry inhibitor of HIV-1, but is only partially responsible for interferon's suppressive effect6-8. Using small interfering RNA-based library screening in interferon-α-treated cells, we sought to characterize further interferon-stimulated genes that target the pre-integration phases of HIV-1 infection, and identified human tripartite-containing motif 5α (TRIM5α) as a potent anti-HIV-1 restriction factor. Human TRIM5α, in contrast with many nonhuman orthologues, has not generally been ascribed substantial HIV-1 inhibitory function, a finding attributed to ineffective recognition of cytoplasmic viral capsids by TRIM5α2,9,10. Here, we demonstrate that interferon-α-mediated stimulation of the immunoproteasome, a proteasome isoform mainly present in immune cells and distinguished from the constitutive proteasome by virtue of its different catalytic β-subunits, as well as the proteasome activator 28 regulatory complex11-13, and the associated accelerated turnover of TRIM5α underpin the reprogramming of human TRIM5α for effective capsid-dependent inhibition of HIV-1 DNA synthesis and infection. These observations identify a mechanism for regulating human TRIM5α antiviral function in human cells and rationalize how TRIM5α participates in the immune control of HIV-1 infection.</dc:description>
      <dc:date>2024-09-28T17:37:48Z</dc:date>
      <dc:date>2024-09-28T17:37:48Z</dc:date>
      <dc:date>2019</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Jimenez-Guardeño, J.M., Apolonia, L., Betancor, G. et al. Immunoproteasome activation enables human TRIM5α restriction of HIV-1. Nat Microbiol 4, 933–940 (2019). https://doi.org/10.1038/s41564-019-0402-0</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/33866</dc:identifier>
      <dc:identifier>10.1038/s41564-019-0402-0</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
      <dc:publisher>Springer Nature</dc:publisher>
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