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Evolutionary diversification of the autophagy-related ubiquitin-like conjugation systems

机译:自噬相关泛素样偶联系统的进化多样化

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摘要

Two autophagy-related (ATG) ubiquitin-like conjugation systems, the ATG12 and ATG8 systems, play important roles in macroautophagy. While multiple duplications and losses of the ATG conjugation system proteins are found in different lineages, the extent to which the underlying systems diversified across eukaryotes is not fully understood. Here, in order to understand the evolution of the ATG conjugation systems, we constructed a transcriptome database consisting of 94 eukaryotic species covering major eukaryotic clades and systematically identified ATG conjugation system components. Both ATG10 and the C-terminal glycine of ATG12 are essential for the canonical ubiquitin-like conjugation of ATG12 and ATG5. However, loss of ATG10 or the C-terminal glycine of ATG12 occurred at least 16 times in a wide range of lineages, suggesting that possible covalent-to-non-covalent transition is not limited to the species that we previously reported such as Alveolata and some yeast species. Some species have only the ATG8 system (with conjugation enzymes) or only ATG8 (without conjugation enzymes). More than 10 species have ATG8 homologs without the conserved C-terminal glycine, and Tetrahymena has an ATG8 homolog with a predicted transmembrane domain, which may be able to anchor to the membrane independent of the ATG conjugation systems. We discuss the possibility that the ancestor of the ATG12 and ATG8 systems is more similar to ATG8. Overall, our study offers a whole picture of the evolution and diversity of the ATG conjugation systems among eukaryotes, and provides evidence that functional diversifications of the systems are more common than previously thought.Abbreviations: APEAR: ATG8–PE association region; ATG: autophagy-related; LIR: LC3-interacting region; NEDD8: neural precursor cell expressed, developmentally down-regulated gene 8; PE: phosphatidylethanolamine; SAMP: small archaeal modifier protein; SAR: Stramenopiles, Alveolata, and Rhizaria; SMC: structural maintenance of chromosomes; SUMO: small ubiquitin like modifier; TACK: Thaumarchaeota, Aigarchaeota, Crenarchaeota, and Korarchaeota; UBA: ubiquitin like modifier activating enzyme; UFM: ubiquitin fold modifier; URM: ubiquitin related modifier.
机译:两种自噬相关 (ATG) 泛素样偶联系统,即 ATG12 和 ATG8 系统,在巨自噬中起着重要作用。虽然在不同的谱系中发现了 ATG 偶联系统蛋白的多次重复和丢失,但基础系统在真核生物中多样化的程度尚不完全清楚。在这里,为了了解 ATG 偶联系统的进化,我们构建了一个转录组数据库,该数据库由 94 个真核物种组成,涵盖了主要的真核生物分支和系统鉴定的 ATG 偶联系统成分。ATG10 和 ATG12 的 C 端甘氨酸对于 ATG12 和 ATG5 的经典泛素样偶联至关重要。然而,ATG10 或 ATG12 的 C 端甘氨酸丢失在广泛的谱系中至少发生了 16 次,这表明可能的共价到非共价转变不仅限于我们之前报道的物种,例如肺泡和一些酵母物种。一些物种只有 ATG8 系统(有偶联酶)或只有 ATG8(没有偶联酶)。超过 10 个物种具有没有保守 C 端甘氨酸的 ATG8 同源物,而 Tetrahymena 具有具有预测跨膜结构域的 ATG8 同源物,它可能能够独立于 ATG 偶联系统锚定到膜上。我们讨论了 ATG12 和 ATG8 系统的祖先与 ATG8 更相似的可能性。总体而言,我们的研究提供了真核生物中 ATG 偶联系统进化和多样性的全貌,并提供了系统的功能多样化比以前认为的更普遍的证据。缩写: APEAR:ATG8–PE 关联地区;ATG: 自噬相关;LIR: LC3 相互作用区;NEDD8: 神经前体细胞表达的发育下调基因 8;PE: 磷脂酰乙醇胺;SAMP: 小古细菌修饰蛋白;SAR:Stramenopiles、Alveolata 和 Rhizaria;SMC: 染色体的结构维护;SUMO: 小泛素样修饰剂;TACK:Thaumarchaeota、Aigarchaeota、Crenarchaeota 和 Korarchaeota;UBA: 泛素样修饰物激活酶;UFM: 泛素折叠修饰剂;URM: 泛素相关修饰剂。

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