Boopathi Ettickan, Srinivasan Satish, Fang Ji-Kang, Avadhani Narayan G
Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Mol Cell. 2008 Oct 10;32(1):32-42. doi: 10.1016/j.molcel.2008.09.008.
Bimodal targeting of the endoplasmic reticular protein, cytochrome P4501A1 (CYP1A1), to mitochondria involves activation of a cryptic mitochondrial targeting signal through endoprotease processing of the protein. Here, we characterized the endoprotease that regulates mitochondrial targeting of CYP1A1. The endoprotease, which was induced by beta-naphthoflavone, was a dimer of 90 kDa and 40 kDa subunits, each containing Ser protease domains. The purified protease processed CYP1A1 in a sequence-specific manner, leading to its mitochondrial import. The glucocorticoid receptor, retinoid X receptor, and p53 underwent similar processing-coupled mitochondrial transport. The inducible 90 kDa subunit was a limiting factor in many cells and some tissues and, thus, regulates the mitochondrial levels of these proteins. A number of other mitochondria-associated proteins with noncanonical targeting signals may also be substrates of this endoprotease. Our results describe a new mechanism of mitochondrial protein import that requires an inducible cytoplasmic endoprotease for activation of cryptic mitochondrial targeting signals.
内质网蛋白细胞色素P4501A1(CYP1A1)靶向线粒体的双峰机制涉及通过该蛋白的内切蛋白酶加工激活一个隐蔽的线粒体靶向信号。在此,我们对调节CYP1A1线粒体靶向的内切蛋白酶进行了表征。该内切蛋白酶由β-萘黄酮诱导产生,是一个由90 kDa和40 kDa亚基组成的二聚体,每个亚基都含有丝氨酸蛋白酶结构域。纯化后的蛋白酶以序列特异性方式加工CYP1A1,使其能够导入线粒体。糖皮质激素受体、视黄酸X受体和p53也经历了类似的加工偶联线粒体转运过程。在许多细胞和一些组织中,可诱导的90 kDa亚基是一个限制因素,因此它调节这些蛋白质的线粒体水平。许多其他具有非经典靶向信号的线粒体相关蛋白也可能是这种内切蛋白酶的底物。我们的结果描述了一种线粒体蛋白导入的新机制,该机制需要一种可诱导的细胞质内切蛋白酶来激活隐蔽的线粒体靶向信号。