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SUD1 基因编码一个假定的 E3 泛素连接酶,是拟南芥中 3-羟基-3-甲基戊二酰辅酶 A 还原酶活性的正调控因子。

The SUD1 gene encodes a putative E3 ubiquitin ligase and is a positive regulator of 3-hydroxy-3-methylglutaryl coenzyme a reductase activity in Arabidopsis.

机构信息

Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga-Consejo Superior de Investigaciones Científicas, Departamento de Biología Molecular y Bioquímica, Facultad de Ciencias, Universidad de Málaga, 29071 Malaga, Spain.

出版信息

Plant Cell. 2013 Feb;25(2):728-43. doi: 10.1105/tpc.112.108696. Epub 2013 Feb 12.

DOI:10.1105/tpc.112.108696
PMID:23404890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3608789/
Abstract

The 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) enzyme catalyzes the major rate-limiting step of the mevalonic acid (MVA) pathway from which sterols and other isoprenoids are synthesized. In contrast with our extensive knowledge of the regulation of HMGR in yeast and animals, little is known about this process in plants. To identify regulatory components of the MVA pathway in plants, we performed a genetic screen for second-site suppressor mutations of the Arabidopsis thaliana highly drought-sensitive drought hypersensitive2 (dry2) mutant that shows decreased squalene epoxidase activity. We show that mutations in SUPPRESSOR OF DRY2 DEFECTS1 (SUD1) gene recover most developmental defects in dry2 through changes in HMGR activity. SUD1 encodes a putative E3 ubiquitin ligase that shows sequence and structural similarity to yeast Degradation of α factor (Doα10) and human TEB4, components of the endoplasmic reticulum-associated degradation C (ERAD-C) pathway. While in yeast and animals, the alternative ERAD-L/ERAD-M pathway regulates HMGR activity by controlling protein stability, SUD1 regulates HMGR activity without apparent changes in protein content. These results highlight similarities, as well as important mechanistic differences, among the components involved in HMGR regulation in plants, yeast, and animals.

摘要

3-羟-3-甲基戊二酰辅酶 A 还原酶(HMGR)酶催化甲羟戊酸(MVA)途径中的主要限速步骤,该途径合成固醇和其他异戊二烯。与我们对酵母和动物中 HMGR 调节的广泛了解相比,对植物中这一过程知之甚少。为了鉴定植物 MVA 途径的调节成分,我们对拟南芥高度干旱敏感的干旱敏感 2(dry2)突变体的第二位点抑制突变进行了遗传筛选,该突变体显示出鲨烯环氧化酶活性降低。我们表明,SUPPRESSOR OF DRY2 DEFECTS1(SUD1)基因突变通过改变 HMGR 活性恢复了 dry2 中的大多数发育缺陷。SUD1 编码一种假定的 E3 泛素连接酶,它与酵母 Degradation of α factor(Doα10)和人类 TEB4 具有序列和结构相似性,后者是内质网相关降解 C(ERAD-C)途径的组成部分。虽然在酵母和动物中,替代的 ERAD-L/ERAD-M 途径通过控制蛋白质稳定性来调节 HMGR 活性,但 SUD1 调节 HMGR 活性而蛋白质含量没有明显变化。这些结果突出了植物、酵母和动物中参与 HMGR 调节的成分之间的相似性,以及重要的机制差异。

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