Both K63 and K48 ubiquitin linkages signal lysosomal degradation of the LDL receptor

Li Zhang, Ming Xu, Elena Scotti, Zhijian J. Chen, Peter Tontonoz

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Linkage-specific ubiquitination often leads to distinct cellular events. It has been difficult to establish definitively the requirement for a particular linkage in mammalian degradation pathways due to the inability to deplete endogenous ubiquitin while maintaining cell viability. The E3 ubiquitin ligase inducible degrader of the LDL receptor (IDOL) targets the low density lipoprotein receptor (LDLR) for degradation. The nature of the linkages employed to signal lysosomal degradation of the LDLR, and to signal proteasomal autodegradation of IDOL, have not been determined. We used an inducible RNAi strategy to replace endogenous ubiquitin with mutants lacking K48 or K63. We found that IDOL catalyzes the transfer of ubiquitin chains to itself and to the LDLR that do not contain exclusively K48 or K63 linkages. Thus, LDLR can be targeted to the lysosome by either K48 or K63 linkages. We further demonstrate that although both ubiquitin conjugating enzyme E2 (UBE2)Ds and UBE2N/V1 can catalyze LDLR ubiquitination in a cell-free system, UBE2Ds appear to be the major E2 enzymes employed by IDOL in cells, consistent with their ability to catalyze both K48 and K63 linkages. The results reveal mechanistic insight into the posttranscriptional control of lipoprotein uptake and provide a test of the requirement of linkage-specific ubiquitination for specific lysosomal and proteasomal degradation pathways in mammalian cells.

Original languageEnglish (US)
Pages (from-to)1410-1420
Number of pages11
JournalJournal of Lipid Research
Volume54
Issue number5
DOIs
StatePublished - May 2013

Fingerprint

LDL Receptors
Ubiquitin
Degradation
Ubiquitination
Cells
Ubiquitin-Conjugating Enzymes
Ubiquitin-Protein Ligases
Cell-Free System
RNA Interference
Lysosomes
Lipoproteins
Cell Survival
Enzymes

Keywords

  • E3 ubiquitinligase
  • Low density lipoprotein receptor
  • Lysosomal protein degradation
  • Proteasomal protein degradation

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Endocrinology

Cite this

Both K63 and K48 ubiquitin linkages signal lysosomal degradation of the LDL receptor. / Zhang, Li; Xu, Ming; Scotti, Elena; Chen, Zhijian J.; Tontonoz, Peter.

In: Journal of Lipid Research, Vol. 54, No. 5, 05.2013, p. 1410-1420.

Research output: Contribution to journalArticle

Zhang, Li ; Xu, Ming ; Scotti, Elena ; Chen, Zhijian J. ; Tontonoz, Peter. / Both K63 and K48 ubiquitin linkages signal lysosomal degradation of the LDL receptor. In: Journal of Lipid Research. 2013 ; Vol. 54, No. 5. pp. 1410-1420.
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