E2-25K mediates US11-triggered retro-translocation of MHC class I heavy chains in a permeabilized cell system
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Author
Flierman, Dennis
Coleman, Catherine S.
Pickart, Cecile M.
Rapoport, Tom A.
Chau, Vincent
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https://doi.org/10.1073/pnas.0605215103Metadata
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Flierman, D., C. S. Coleman, C. M. Pickart, T. A. Rapoport, and V. Chau. 2006. “E2-25K Mediates US11-Triggered Retro-Translocation of MHC Class I Heavy Chains in a Permeabilized Cell System.” Proceedings of the National Academy of Sciences 103 (31): 11589–94. doi:10.1073/pnas.0605215103.Abstract
In cells expressing human cytornegalovirus US11 protein, newly synthesized MHC class I heavy chains (HCs) are rapidly dislocated from the endoplasmic reticulum (ER) and degraded in the cytosol, a process that is similar to ER-associated degradation (ERAD), the pathway used for degradation of misfolded ER proteins. US11-triggered movement of HCs into the cytosol requires polyubiquitination, but it is unknown which ubiquitin-conjugating and ubiquitin-ligase enzymes are involved. To identify the ubiquitin-conjugating enzyme (E2) required for dislocation, we used a permeabilized cell system, in which endogenous cytosol can be replaced by cow liver cytosol. By fractionating the cytosol, we show that E2-25K can serve as the sole E2 required for dislocation of HCs in vitro. Purified recombinant E2-25K, together with components that convert this E2 to the active E2-ubiquitin thiolester form, can substitute for crude cytosol. E2-25K cannot be replaced by the conjugating enzymes HsUbc7/Ube2G2 or UIbe2G1, even though HsUbc7/Ube2G2 and its yeast homolog Ubc7p are known to participate in ERAD. The activity of E2-25K, as measured by ubiquitin dimer formation, is strikingly enhanced when added to permeabilized cells, likely by membrane-bound ubiquitin protein ligases. To identify these ligases, we tested RING domains of various ligases for their activation of E2-25K in vitro. We found that RING domains of gp78/AMFR, a ligase previously implicated in ERAD, and MARCHVII/axotrophin, a ligase of unknown function, greatly enhanced the activity of E2-25K. We conclude that in permeabilized, US11-expressing cells polyubiquitination of the HC substrate can be catalyzed by E2-25K, perhaps in cooperation with the ligase MARCHVII/axotrophin.Terms of Use
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