首页> 外文期刊>Plant and cell physiology >A Negative Regulator in Response to Salinity in Rice: Oryza sativa Salt-, ABA- and Drought-Induced RING Finger Protein 1 (OsSADR1)
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A Negative Regulator in Response to Salinity in Rice: Oryza sativa Salt-, ABA- and Drought-Induced RING Finger Protein 1 (OsSADR1)

机译:响应水稻盐度的负调节剂:Oryza sativa盐 - ,aba-和干旱诱导的无名指蛋白1(OSSADR1)

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RING (Really Interesting New Gene) finger proteins play crucial roles in abiotic stress responses in plants. We report the RING finger E3 ligase gene, an Oryza sativa salt, ABA and drought stress-induced RING finger protein 1 gene (OsSADR1). We demonstrated that although OsSAR1 possesses E3 ligase activity, a single amino acid substitution (OsSADR1C168A) in the RING domain resulted in no E3 ligase activity, suggesting that the activity of most E3s is specified by the RING domain. Additional assays substantiated that OsSADR1 interacts with three substrates—no E3 ligase acti and OsPIRIN, and mediates their proteolysis via the 26S proteasome pathway. For OsSADR1, approximately 62% of the transient signals were in the cytosol and 38% in the nucleus. However, transiently expressed OsSADR1 was primarily expressed in the nucleus (70%) in 200 mM salt-treated rice protoplasts. The two nucleus-localized proteins (OsSNAC2 and OsGRAS44) interacted with OsSADR1 in the cytosol and nucleus. Heterogeneous overexpression of OsSADR1 in Arabidopsis resulted in sensitive phenotypes for salt- and mannitol-responsive seed germination and seedling growth. With ABA, OsSADR1 overexpression in plants produced highly tolerant phenotypes, with morphological changes in root length and stomatal closure. The ABA-tolerant transgenic plants also showed hypersensitivity phenotypes under severe water deficit conditions. Taken together, OsSADR1 may act as a regulator in abiotic stress responses by modulating target protein levels.
机译:戒指(真正有趣的新基因)手指蛋白在植物中非生物应激反应中起重要作用。我们报告着环手指E3连接酶基因,羚羊苜蓿盐,ABA和干旱应激诱导的无名指蛋白1基因(OSSADR1)。我们证明,虽然OSSAR1具有E3连接酶活性,但环形结构域中的单个氨基酸取代(OSSADR1C168a)导致NO e3连接酶活性,表明大多数E3s的活性由环结构域指定。另外的测定证实,OSSADR1与三种底物 - NO e3连接酶Acti和Osphin相互作用,并通过26s蛋白酶体途径介导它们的蛋白水解。对于OSSADR1,大约62%的瞬态信号在细胞溶胶中,核中的38%。然而,瞬时表达的OSSADR1主要在200mM盐处理水稻原生质体中的核(70%)中表达。两种核局部蛋白(OSSNAC2和OSGRAS44)与胞嘧啶和核中的OSSADR1相互作用。拟南芥OSSADR1的异质过度表达导致盐和甘露醇响应种子萌发和幼苗生长的敏感表型。随着ABA,植物中的OSSADR1过表达产生高度耐受性表型,具有根长和气孔闭合的形态变化。 ABA耐性转基因植物在严重的水缺陷条件下也显示出过敏表型。携带在一起,OSSADR1可以通过调节靶蛋白水平作为非生物应激反应的调节因子。

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