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Skp1 被细胞质脯氨酰 4(反式)羟化酶和α-N-乙酰氨基葡萄糖基转移酶加工的要求涉及到 Dictyostelium 中的 O₂信号转导。

Requirements for Skp1 processing by cytosolic prolyl 4(trans)-hydroxylase and α-N-acetylglucosaminyltransferase enzymes involved in O₂ signaling in dictyostelium.

机构信息

Department of Biochemistry and Molecular Biology, Oklahoma Center for Medical Glycobiology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, United States.

出版信息

Biochemistry. 2011 Mar 15;50(10):1700-13. doi: 10.1021/bi101977w. Epub 2011 Feb 9.

Abstract

The social amoeba Dictyostelium expresses a hypoxia inducible factor-α (HIFα) type prolyl 4-hydroxylase (P4H1) and an α-N-acetylglucosaminyltransferase (Gnt1) that sequentially modify proline-143 of Skp1, a subunit of the SCF (Skp1/Cullin/F-box protein) class of E3 ubiquitin ligases. Prior genetic studies have implicated Skp1 and its modification by these enzymes in O(2) regulation of development, suggesting the existence of an ancient O(2)-sensing mechanism related to modification of the transcription factor HIFα by animal prolyl 4-hydroxylases (PHDs). To better understand the role of Skp1 in P4H1-dependent O(2) signaling, biochemical and biophysical studies were conducted to characterize the reaction product and the basis of Skp1 substrate selection by P4H1 and Gnt1. (1)H NMR demonstrated formation of 4(trans)-hydroxyproline as previously found for HIFα, and highly purified P4H1 was inhibited by Krebs cycle intermediates and other compounds that affect animal P4Hs. However, in contrast to hydroxylation of HIFα by PHDs, P4H1 depended on features of full-length Skp1, based on truncation, mutagenesis, and competitive inhibition studies. These features are conserved during animal evolution, as even mammalian Skp1, which lacks the target proline, became a good substrate upon its restoration. P4H1 recognition may depend on features conserved for SCF complex formation as heterodimerization with an F-box protein blocked Skp1 hydroxylation. The hydroxyproline-capping enzyme Gnt1 exhibited similar requirements for Skp1 as a substrate. These and other findings support a model in which the protist P4H1 conditionally hydroxylates Skp1 of E3(SCF)ubiquitin ligases to control half-lives of multiple targets, rather than the mechanism of animal PHDs where individual proteins are hydroxylated leading to ubiquitination by the evolutionarily related E3(VBC)ubiquitin ligases.

摘要

粘菌 Dictyostelium 表达一种缺氧诱导因子-α(HIFα)类型的脯氨酰 4-羟化酶(P4H1)和一种α-N-乙酰氨基葡萄糖基转移酶(Gnt1),它们依次修饰 Skp1 的脯氨酸-143,Skp1 是 SCF(Skp1/Cullin/F-box 蛋白)类 E3 泛素连接酶的一个亚基。先前的遗传研究表明,Skp1 及其被这些酶修饰在 O2 调节发育中起作用,这表明存在一种与动物脯氨酰 4-羟化酶(PHD)修饰转录因子 HIFα相关的古老 O2 感应机制。为了更好地理解 Skp1 在 P4H1 依赖性 O2 信号传导中的作用,进行了生化和生物物理研究,以表征反应产物以及 P4H1 和 Gnt1 对 Skp1 底物选择的基础。(1)H NMR 证明了 4(trans)-羟脯氨酸的形成,如先前在 HIFα 中发现的那样,并且高度纯化的 P4H1 被克雷布斯循环中间产物和其他影响动物 P4Hs 的化合物抑制。然而,与 PHDs 对 HIFα 的羟化作用相反,P4H1 基于截断、突变和竞争抑制研究,依赖于全长 Skp1 的特征。这些特征在动物进化过程中是保守的,因为即使是缺乏靶标脯氨酸的哺乳动物 Skp1,在其恢复后也成为良好的底物。P4H1 的识别可能依赖于 SCF 复合物形成的保守特征,因为与 F-box 蛋白的异二聚化阻止了 Skp1 的羟化。羟脯氨酸加帽酶 Gnt1 作为底物对 Skp1 表现出类似的要求。这些和其他发现支持这样一种模型,即原生动物 P4H1 有条件地羟化 E3(SCF)泛素连接酶的 Skp1,以控制多个靶标的半衰期,而不是动物 PHDs 的机制,其中单个蛋白质被羟化,导致与进化相关的 E3(VBC)泛素连接酶的泛素化。

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