The QKI-PLP pathway controls SIRT2 abundance in CNS myelin

• Type of Material: Article
• Authors: H Zhu, University of Kentucky; L Zhao, Emory University; E Wang, University of Kentucky; N Dimova, University of Kentucky; G Liu, Emory University; Yue Feng, Emory University; F Cambi, University of Kentucky
• Language: English
• Date: 2012-01
• Publisher: Wiley: 12 months
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2011 Wiley Periodicals, Inc.
• Final Published Version (URL): http://dx.doi.org/10.1002%2Fglia.21248
• Title of Journal or Parent Work: Glia
• ISSN: 0894-1491
• Volume: 60
• Issue: 1
• Start Page: 69
• End Page: 82
• Grant/Funding Information: This work was supported by NIH/NINDS (RO1NS053905) to FC and European Leukodystrophy Association (2008-013I1) to FC and EW, NIH/NINDS (R01NS056097) and NMSS (RG4010-A-2) to YF.
• Keywords: myelin; PLP; Sirtuin2; quaking; oligodendrocytes; development
• Research Categories: Health Sciences, Pathology

Abstract

Sirtuin 2 (SIRT2), a NAD-dependent deacetylase expressed by oligodendrocytes (OLs), the myelin-producing cells of the central nervous system (CNS), is markedly up-regulated during active myelination (Li et al. 2007; Southwood et al. 2007; Werner et al. 2007). SIRT2 is a component of the myelin proteome and is severely reduced in the Plp1 knockout mouse brain, in which both PLP and DM20 are absent (Werner et al. 2007). The mechanisms that regulate SIRT2 expression in OLs and myelin remain to be investigated. We report for the first time that the expression of SIRT2 is regulated by the QKI-dependent pathway and this effect is mediated through selective regulation of PLP. In the homozygous quakingviable (qkv/qkv) mutant mouse that harbors QKI deficiency in OLs (Bockbrader and Feng 2008; Ebersole et al. 1996; Hardy et al. 1996), PLP, but not DM20 mRNA, was selectively down-regulated and SIRT2 protein was severely reduced while SIRT2 mRNA expression was unaffected. Expression of the cytoplasmic isoform QKI6 in OLs (Zhao et al. 2006) rescued SIRT2 expression in the qkv/qkv mutant concomitantly with restoration of PLP expression. Moreover, SIRT2 protein is diminished in myelin tracts and compact myelin of the PLP-ISEdel mutant brain, in which PLP protein but not DM20 is selectively reduced (Wang et al. 2008). In contrast, SIRT2 expression and its cellular function in regulating process complexity are not affected by the absence of PLP in PLP-ISEdel non-myelinating oligodendrocytes. Collectively, our results indicate that the abundance of SIRT2 in myelin is dependent on PLP, but not DM20.