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首页> 外文期刊>The Plant Cell >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.
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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.

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

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摘要

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 alpha factor (Do alpha 10) 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.
机译:3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)催化甲羟戊酸(MVA)途径的主要限速步骤,从该步骤合成甾醇和其他类异戊二烯。与我们对酵母和动物中HMGR调控的广泛了解相反,对于植物中的该过程知之甚少。为了确定植物中MVA途径的调控成分,我们对拟南芥高度干旱敏感的干旱超敏2(dry2)突变株的第二位抑制子突变进行了基因筛选,该突变显示了角鲨烯环氧酶活性降低。我们显示,DRY2 DEFECTS1(SUD1)基因抑制子中的突变通过改变HMGR活性来恢复dry2的大多数发育缺陷。 SUD1编码一个推定的E3泛素连接酶,该酶显示与酵母降解的序列和结构相似性α因子(Do alpha 10)和人TEB4,这是内质网相关降解C(ERAD-C)途径的组成部分。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,而SUD1则在没有蛋白质含量明显变化的情况下调节HMGR活性。这些结果突显了植物,酵母和动物中HMGR调控所涉及的成分之间的相似性以及重要的机理差异。

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