School of Biological Sciences, University of Liverpool, Liverpool, UK.
FEBS Lett. 2010 Jul 16;584(14):2981-9. doi: 10.1016/j.febslet.2010.05.061. Epub 2010 Jun 11.
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.
细胞凋亡是一种基本的生物学现象,受到多种因素的复杂调控。髓样细胞白血病 1(Mcl-1)是 B 细胞淋巴瘤 2(Bcl-2)家族中一种抗凋亡蛋白,它体现了许多蛋白质对细胞命运的贡献可以被修饰的机制。Mcl-1 的 N 端在 Bcl-2 家族中是独特的,因为它富含实验证实和推测的调节残基和基序。这些包括泛素化、切割和磷酸化的位点,这些修饰影响蛋白质的稳定性、定位、二聚化和功能。本文综述了 Mcl-1 表达和功能的调控,特别关注了翻译后修饰以及磷酸化如何将 Mcl-1 的复杂分子调控与细胞状态联系起来。