Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit

Rick Nelson, Kevin A. Glenn, Yuzhou Zhang, Hsiang Wen, Tina Knutson, Cynthia M. Gouvion, Barbara K. Robinson, Zouping Zhou, Baoli Yang, Richard J H Smith, Henry L. Paulson

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Little is known about the role of protein quality control in the inner ear. We now report selective cochlear degeneration in mice deficient in Fbx2, a ubiquitin ligase F-box protein with specificity for high-mannose glycoproteins (Yoshida et al., 2002). Originally described as a brain-enriched protein (Erhardt et al., 1998), Fbx2 is also highly expressed in the organ of Corti, in which it has been called organ of Corti protein 1 (Thalmann et al., 1997). Mice with targeted deletion of Fbxo2 develop age-related hearing loss beginning at 2 months. Cellular degeneration begins in the epithelial support cells of the organ of Corti and is accompanied by changes in cellular membrane integrity and early increases in connexin 26, a cochlear gap junction protein previously shown to interact with Fbx2 (Henzl et al., 2004). Progressive degeneration includes hair cells and the spiral ganglion, but the brain itself is spared despite widespread CNS expression of Fbx2. Cochlear Fbx2 binds Skp1, the common binding partner for F-box proteins, and is an unusually abundant inner ear protein. Whereas cochlear Skp1 levels fall in parallel with the loss of Fbx2, other components of the canonical SCF (Skp1, Cullin1, F-box, Rbx1) ubiquitin ligase complex remain unchanged and show little if any complex formation with Fbx2/Skp1, suggesting that cochlear Fbx2 and Skp1 form a novel, heterodimeric complex. Our findings demonstrate that components of protein quality control are essential for inner ear homeostasis and implicate Fbx2 and Skp1 as potential genetic modifiers in age-related hearing loss.

Original languageEnglish (US)
Pages (from-to)5163-5171
Number of pages9
JournalJournal of Neuroscience
Volume27
Issue number19
DOIs
StatePublished - May 9 2007
Externally publishedYes

Fingerprint

F-Box Proteins
Cochlea
Ligases
Ubiquitin
Glycoproteins
Organ of Corti
Inner Ear
Proteins
Hearing Loss
Quality Control
Spiral Ganglion
Connexins
Brain
Mannose
Homeostasis
Epithelial Cells
Membranes

Keywords

  • Deafness
  • Degradation
  • Fbx2
  • Glycoprotein
  • Skp1
  • Ubiquitin

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit. / Nelson, Rick; Glenn, Kevin A.; Zhang, Yuzhou; Wen, Hsiang; Knutson, Tina; Gouvion, Cynthia M.; Robinson, Barbara K.; Zhou, Zouping; Yang, Baoli; Smith, Richard J H; Paulson, Henry L.

In: Journal of Neuroscience, Vol. 27, No. 19, 09.05.2007, p. 5163-5171.

Research output: Contribution to journalArticle

Nelson, R, Glenn, KA, Zhang, Y, Wen, H, Knutson, T, Gouvion, CM, Robinson, BK, Zhou, Z, Yang, B, Smith, RJH & Paulson, HL 2007, 'Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit', Journal of Neuroscience, vol. 27, no. 19, pp. 5163-5171. https://doi.org/10.1523/JNEUROSCI.0206-07.2007
Nelson, Rick ; Glenn, Kevin A. ; Zhang, Yuzhou ; Wen, Hsiang ; Knutson, Tina ; Gouvion, Cynthia M. ; Robinson, Barbara K. ; Zhou, Zouping ; Yang, Baoli ; Smith, Richard J H ; Paulson, Henry L. / Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit. In: Journal of Neuroscience. 2007 ; Vol. 27, No. 19. pp. 5163-5171.
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