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Alliance"],"published-print":{"date-parts":[[2024,4]]},"abstract":"<jats:p>The cellular response to a decrease in protein degradation by 26S proteasomes in chronic diseases is poorly understood. Pharmacological inhibition of proteasomes increases the expression of proteasome subunits and Proteasome Activator 200 (PA200), an alternative proteasome activator. In the S63del mouse model of the peripheral neuropathy Charcot Marie Tooth 1B (CMT1B), proteasomal protein degradation is decreased and proteasome gene expression is increased. Here, we show an increase in PA200 and PA200-bound proteasomes in the peripheral nerves of S63del mice. To test genetically whether the upregulation of PA200 was compensatory, we generated S63del\/\/PA200\u2212\/\u2212 mice. Unexpectedly, in the sciatic nerves of these mice, there was greater proteasomal protein degradation than in S63del, less polyubiquitinated proteins and markers of the unfolded protein response, and a greater amount of assembled, active 26S proteasomes. These changes were not seen in PA200\u2212\/\u2212 controls and were therefore specific to the neuropathy. Furthermore, in S63del\/\/PA200\u2212\/\u2212 mice, myelin thickness and nerve conduction were restored to WT levels. Thus, the upregulation of PA200 is maladaptive in S63del mice and its genetic ablation prevented neuropathy.<\/jats:p>","DOI":"10.26508\/lsa.202302349","type":"journal-article","created":{"date-parts":[[2024,2,6]],"date-time":"2024-02-06T12:39:47Z","timestamp":1707223187000},"page":"e202302349","update-policy":"https:\/\/doi.org\/10.26508\/lsa.crossmarkpolicy","source":"Crossref","is-referenced-by-count":8,"title":["Knockout of PA200 improves proteasomal degradation and myelination in a proteotoxic neuropathy"],"prefix":"10.26508","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4411-2659","authenticated-orcid":true,"given":"Jordan JS","family":"VerPlank","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01y64my43","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Biochemistry, Institute for Myelin and Glia Exploration, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo","place":[", Buffalo, NY, 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