Ubc13 and COOH terminus of Hsp70-interacting protein (CHIP) are required for growth hormone receptor endocytosis

Growth hormone receptor (GHR) endocytosis is a highly regulated process that depends on the binding and activity of the multimeric ubiquitin ligase, SCF(βTrCP) (Skp Cullin F-box). Despite a specific interaction between β-transducin repeat-containing protein (βTrCP) and the GHR, and a strict requirem...

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Veröffentlicht in:The Journal of biological chemistry Jg. 287; H. 19; S. 15533
Hauptverfasser: Slotman, Johan A, da Silva Almeida, Ana C, Hassink, Gerco C, van de Ven, Robert H A, van Kerkhof, Peter, Kuiken, Hendrik J, Strous, Ger J
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 04.05.2012
Schlagworte:
beta-Transducin Repeat-Containing Proteins - genetics
beta-Transducin Repeat-Containing Proteins - metabolism
Blotting, Western
Cell Line, Tumor
Endocytosis
Humans
Lysine - metabolism
Microscopy, Fluorescence
Protein Binding
Protein Multimerization
Receptors, Somatotropin - chemistry
Receptors, Somatotropin - genetics
Receptors, Somatotropin - metabolism
RNA Interference
Ubiquitin-Conjugating Enzymes - genetics
Ubiquitin-Conjugating Enzymes - metabolism
Ubiquitin-Protein Ligases - genetics
Ubiquitin-Protein Ligases - metabolism
Ubiquitination
ISSN:1083-351X, 1083-351X
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Zusammenfassung:Growth hormone receptor (GHR) endocytosis is a highly regulated process that depends on the binding and activity of the multimeric ubiquitin ligase, SCF(βTrCP) (Skp Cullin F-box). Despite a specific interaction between β-transducin repeat-containing protein (βTrCP) and the GHR, and a strict requirement for ubiquitination activity, the receptor is not an obligatory target for SCF(βTrCP)-directed Lys(48) polyubiquitination. We now show that also Lys(63)-linked ubiquitin chain formation is required for GHR endocytosis. We identified both the ubiquitin-conjugating enzyme Ubc13 and the ubiquitin ligase COOH terminus of Hsp70 interacting protein (CHIP) as being connected to this process. Ubc13 activity and its interaction with CHIP precede endocytosis of GHR. In addition to βTrCP, CHIP interacts specifically with the cytosolic tails of the dimeric GHR, identifying both Ubc13 and CHIP as novel factors in the regulation of cell surface availability of GHR.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1083-351X
1083-351X
DOI:10.1074/jbc.M111.302521