4.8 Article

Stable and unstable pools of Myc protein exist in human cells

Journal

ONCOGENE
Volume 21, Issue 55, Pages 8515-8520

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1205976

Keywords

Myc; Max; ubiquitin-mediated proteolysis

Funding

  1. NCI NIH HHS [CA-13106, CA45508] Funding Source: Medline
  2. NIGMS NIH HHS [1T32-GM08468] Funding Source: Medline

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The oncoprotein transcription factor Myc plays a crucial role in the control of cell growth and proliferation. Consistent with its potent growth-promoting properties, cells have evolved a number of mechanisms to limit the activity and accumulation of the Myc protein. One of the most striking of these mechanisms is ubiquitin (Ub)-mediated proteolysis, which typically destroys Myc within minutes of its synthesis. Here we show that, despite the extreme instability of the Myc protein, cells contain a pool of Myc that is metabolically stable. Entry of Myc into the stable pool is signaled by an element within the carboxy-terminus of the protein, and is a cell-specific process that is regulated during mitosis and by interaction with Max. These data demonstrate that even for a rapidly turned-over protein such as Myc metabolically stable and unstable forms of a protein can co-exist in cells, and suggest that the rate of destruction of Myc molecules is linked to their specific functions.

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