Aitchison J D, Nuttley W M, Szilard R K, Brade A M, Glover J R, Rachubinski R A
Department of Biochemistry, McMaster University, Hamilton, Ontario, Canada.
Mol Microbiol. 1992 Dec;6(23):3455-60. doi: 10.1111/j.1365-2958.1992.tb01780.x.
Eukaryotic cells have evolved a complex set of intracellular organelles, each of which possesses a specific complement of enzymes and performs unique metabolic functions. This compartmentalization of cellular functions provides a level of metabolic control not available to prokaryotes. However, it presents the eukaryotic cell with the problem of targeting proteins to their specific location(s). Proteins must be efficiently transported from their site of synthesis in the cytosol to their specific organelle(s). Such a process may require translocation across one or more hydrophobic membrane barriers and/or asymmetric integration into specific membranes. Proteins carry cis-acting amino acid sequences that serve to act as recognition motifs for protein sorting and for the cellular translocation machinery. Sequences that target proteins to the endoplasmic reticulum/secretory pathway, mitochondria, and chloroplasts are often present as cleavable amino-terminal extensions. In contrast, most peroxisomal proteins are synthesized at their mature size and are translocated to the organelle without any post-translational modification. This review will summarize what is known about how yeast solve the problem of specifically importing proteins into peroxisomes and will suggest future directions for investigations into peroxisome biogenesis in yeast.
真核细胞进化出了一套复杂的细胞内细胞器,每个细胞器都拥有特定的酶组合并执行独特的代谢功能。细胞功能的这种区室化提供了原核生物所没有的代谢控制水平。然而,这给真核细胞带来了将蛋白质靶向其特定位置的问题。蛋白质必须从其在细胞质中的合成位点有效地运输到其特定的细胞器。这样的过程可能需要穿过一个或多个疏水膜屏障和/或不对称整合到特定膜中。蛋白质携带顺式作用氨基酸序列,这些序列用作蛋白质分选和细胞转运机制的识别基序。将蛋白质靶向内质网/分泌途径、线粒体和叶绿体的序列通常以可裂解的氨基末端延伸形式存在。相比之下,大多数过氧化物酶体蛋白以其成熟大小合成,并在没有任何翻译后修饰的情况下转运到细胞器中。本综述将总结关于酵母如何解决将蛋白质特异性导入过氧化物酶体这一问题的已知信息,并将提出未来研究酵母过氧化物酶体生物发生的方向。