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Mcl-1; the molecular regulation of protein function

Journal

FEBS LETTERS
Volume 584, Issue 14, Pages 2981-2989

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.febslet.2010.05.061

Keywords

Apoptosis; Post-translational modification; Myeloid cell leukemia 1; Phosphorylation

Funding

  1. Leukemia and Lymphoma Research
  2. Arthritis Research UK

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Apoptosis, an essential and basic biological phenomenon, is regulated in a complex manner by a multitude of factors. Myeloid cell leukemia 1 (Mcl-1), an anti-apoptotic member of the B-cell lymphoma 2 (Bcl-2) family of apoptosis-regulating proteins, exemplifies a number of the mechanisms by which a protein's contribution to cell fate may be modified. The N-terminus of Mcl-1 is unique amongst the Bcl-2 family, in that it is rich in experimentally confirmed and putative regulatory residues and motifs. These include sites for ubiquitination, cleavage and phosphorylation, which influence the protein's stability, localisation, dimerization and function. Here we review what is known about the regulation of Mcl-1 expression and function, with particular focus on post-translational modifications and how phosphorylation interconnects the complex molecular control of Mcl-1 with cellular state. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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