Abstract:
:Myogenesis is conducted by transcription factors including MyoD and myogenin. Myogenin is known to be polyubiquitinated by SCF (Skp1/Cullin 1/F-box protein) followed by proteasomal degradation, though the participating F-box protein is remaining unidentified. In this study, we found that myogenin in differentiated myoblasts is destabilized by muscle atrophy-inducing dexamethasone and that MAFbx (muscle atrophy F-box protein) is increased in atrophying myotubes. MAFbx overexpression resulted in MG132-sensitive reduction of myogenin. Myogenin had a MAFbx-recognition motif and interacted with MAFbx. MAFbx activated polyubiquitination of myogenin. The results of this study suggest that MAFbx functions as an F-box protein for ubiquitination of myogenin.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Jogo M,Shiraishi S,Tamura TAdoi
10.1016/j.febslet.2009.07.033subject
Has Abstractpub_date
2009-09-03 00:00:00pages
2715-9issue
17eissn
0014-5793issn
1873-3468pii
S0014-5793(09)00559-6journal_volume
583pub_type
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