Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Proc Natl Acad Sci U S A. 2024 Sep 24;121(39):e2408697121. doi: 10.1073/pnas.2408697121. Epub 2024 Sep 12.
An N-degron is a degradation signal whose main determinant is a "destabilizing" N-terminal residue of a protein. Specific N-degrons, discovered in 1986, were the first identified degradation signals in short-lived intracellular proteins. These N-degrons are recognized by a ubiquitin-dependent proteolytic system called the Arg/N-degron pathway. Although bacteria lack the ubiquitin system, they also have N-degron pathways. Studies after 1986 have shown that all 20 amino acids of the genetic code can act, in specific sequence contexts, as destabilizing N-terminal residues. Eukaryotic proteins are targeted for the conditional or constitutive degradation by at least five N-degron systems that differ both functionally and mechanistically: the Arg/N-degron pathway, the Ac/N-degron pathway, the Pro/N-degron pathway, the fMet/N-degron pathway, and the newly named, in this perspective, GASTC/N-degron pathway (GASTC = Gly, Ala, Ser, Thr, Cys). I discuss these systems and the expanded terminology that now encompasses the entire gamut of known N-degron pathways.
N 肽段是一种降解信号,其主要决定因素是蛋白质的“不稳定”N 端残基。1986 年发现的特定 N 肽段是最早鉴定的短寿命细胞内蛋白质的降解信号。这些 N 肽段被称为 Arg/N 肽段途径的泛素依赖性蛋白水解系统所识别。尽管细菌缺乏泛素系统,但它们也有 N 肽段途径。1986 年以后的研究表明,遗传密码的所有 20 种氨基酸都可以在特定的序列环境中作为不稳定的 N 端残基发挥作用。至少有五种 N 肽段系统可使真核蛋白质受到条件或组成型降解,这些系统在功能和机制上均有所不同:Arg/N 肽段途径、Ac/N 肽段途径、Pro/N 肽段途径、fMet/N 肽段途径以及新命名的、在这一观点中,GASTC/N 肽段途径(GASTC = Gly、Ala、Ser、Thr、Cys)。我将讨论这些系统以及现在涵盖已知 N 肽段途径全部范围的扩展术语。