Immunoproteasome Assembly: Cooperative Incorporation of Interferon γ (IFN-γ)–inducible Subunits
Open Access
- 5 January 1998
- journal article
- Published by Rockefeller University Press in The Journal of Experimental Medicine
- Vol. 187 (1), 97-104
- https://doi.org/10.1084/jem.187.1.97
Abstract
LMP2, LMP7, and MECL are interferon γ–inducible catalytic subunits of vertebrate 20S proteasomes, which can replace constitutive catalytic subunits (delta, X, and Z, respectively) during proteasome biogenesis. We demonstrate that MECL requires LMP2 for efficient incorporation into preproteasomes, and preproteasomes containing LMP2 and MECL require LMP7 for efficient maturation. The latter effect depends on the presequence of LMP7, but not on LMP7 catalytic activity. This cooperative mechanism favors the assembly of homogeneous “immunoproteasomes” containing all three inducible subunits, suggesting that these subunits act in concert to enhance proteasomal generation of major histocompatibility complex class I–binding peptides.Keywords
This publication has 36 references indexed in Scilit:
- Molecular cloning of the mouse proteasome subunits MC14 and MECL‐1: reciprocally regulated tissue expression of interferon‐γ‐modulated proteasome subunitsEuropean Journal of Immunology, 1997
- Structure of 20S proteasome from yeast at 2.4Å resolutionNature, 1997
- Proteasome Subunits X and Y Alter Peptidase Activities in Opposite Ways to the Interferon-γ-induced Subunits LMP2 and LMP7Published by Elsevier ,1996
- Newly identified pair of proteasomal subunits regulated reciprocally by interferon gamma.The Journal of Experimental Medicine, 1996
- 20S proteasome from LMP7 knock out mice reveals altered proteolytic activities and cleavage site preferencesFEBS Letters, 1996
- Incorporation of major histocompatibility complex – encoded subunits LMP2 and LMP7 changes the quality of the 20S proteasome polypeptide processing products independent of interferon‐γEuropean Journal of Immunology, 1995
- Altered peptidase and viral-specific T cell response in LMP2 mutant miceImmunity, 1994
- MHC Class I Expression in Mice Lacking the Proteasome Subunit LMP-7Science, 1994
- 20 S proteasomes are assembled via distinct precursor complexes processing of LMP2 and LMP7 proproteins takes place in 13–16 S preproteasome complexesJournal of Molecular Biology, 1994
- Post-translational processing of a major histocompatibility complex-encoded proteasome subunit, LMP-2Molecular Immunology, 1993