Young Stephen G, Fong Loren G, Michaelis Susan
Division of Cardiology, Department of Internal Medicine, University of California, Los Angeles, CA 90095, USA.
J Lipid Res. 2005 Dec;46(12):2531-58. doi: 10.1194/jlr.R500011-JLR200. Epub 2005 Oct 5.
Prelamin A undergoes multistep processing to yield lamin A, a structural protein of the nuclear lamina. Prelamin A terminates with a CAAX motif, which triggers farnesylation of a C-terminal cysteine (the C of the CAAX motif), endoproteolytic release of the last three amino acids (the AAX), and methylation of the newly exposed farnesylcysteine residue. In addition, prelamin A is cleaved a second time, releasing 15 more residues from the C terminus (including the farnesylcysteine methyl ester), generating mature lamin A. This second cleavage step is carried out by an endoplasmic reticulum membrane protease, ZMPSTE24. Interest in the posttranslational processing of prelamin A has increased with the recognition that certain progeroid syndromes can be caused by mutations that lead to an accumulation of farnesyl-prelamin A. Recently, we showed that a key cellular phenotype of these progeroid disorders, misshapen cell nuclei, can be ameliorated by inhibitors of protein farnesylation, suggesting a potential strategy for treating these diseases. In this article, we review the posttranslational processing of prelamin A, describe several mouse models for progeroid syndromes, explain the mutations underlying several human progeroid syndromes, and summarize recent data showing that misshapen nuclei can be ameliorated by treating cells with protein farnesyltransferase inhibitors.
前体核纤层蛋白A经过多步加工生成核纤层蛋白A,它是核纤层的一种结构蛋白。前体核纤层蛋白A以CAAX基序结尾,该基序会引发C末端半胱氨酸(CAAX基序中的C)的法尼基化、最后三个氨基酸(AAX)的内切蛋白水解释放以及新暴露的法尼基半胱氨酸残基的甲基化。此外,前体核纤层蛋白A会再次被切割,从C末端释放出另外15个残基(包括法尼基半胱氨酸甲酯),从而产生成熟的核纤层蛋白A。这第二步切割是由内质网膜蛋白酶ZMPSTE24进行的。随着人们认识到某些早老性综合征可能由导致法尼基化前体核纤层蛋白A积累的突变引起,对前体核纤层蛋白A翻译后加工的兴趣也增加了。最近,我们发现这些早老性疾病的一个关键细胞表型——畸形细胞核,可以通过蛋白质法尼基化抑制剂得到改善,这提示了一种治疗这些疾病的潜在策略。在本文中,我们回顾了前体核纤层蛋白A的翻译后加工过程,描述了几种早老性综合征的小鼠模型,解释了几种人类早老性综合征背后的突变,并总结了最近的数据,这些数据表明用蛋白质法尼基转移酶抑制剂处理细胞可以改善畸形细胞核。