首页> 外文OA文献 >Structural, Biochemical, and Phylogenetic Analyses Suggest That Indole-3-Acetic Acid Methyltransferase Is an Evolutionarily Ancient Member of the SABATH Family1[W][OA]
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Structural, Biochemical, and Phylogenetic Analyses Suggest That Indole-3-Acetic Acid Methyltransferase Is an Evolutionarily Ancient Member of the SABATH Family1[W][OA]

机译:结构,生化和系统发育分析表明,吲哚-3-乙酸甲基转移酶是SABATH家族1的进化古老成员。[W] [OA]

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摘要

The plant SABATH protein family encompasses a group of related small-molecule methyltransferases (MTs) that catalyze the S-adenosyl-l-methionine-dependent methylation of natural chemicals encompassing widely divergent structures. Indole-3-acetic acid (IAA) methyltransferase (IAMT) is a member of the SABATH family that modulates IAA homeostasis in plant tissues through methylation of IAA's free carboxyl group. The crystal structure of Arabidopsis (Arabidopsis thaliana) IAMT (AtIAMT1) was determined and refined to 2.75 Å resolution. The overall tertiary and quaternary structures closely resemble the two-domain bilobed monomer and the dimeric arrangement, respectively, previously observed for the related salicylic acid carboxyl methyltransferase from Clarkia breweri (CbSAMT). To further our understanding of the biological function and evolution of SABATHs, especially of IAMT, we analyzed the SABATH gene family in the rice (Oryza sativa) genome. Forty-one OsSABATH genes were identified. Expression analysis showed that more than one-half of the OsSABATH genes were transcribed in one or multiple organs. The OsSABATH gene most similar to AtIAMT1 is OsSABATH4. Escherichia coli-expressed OsSABATH4 protein displayed the highest level of catalytic activity toward IAA and was therefore named OsIAMT1. OsIAMT1 exhibited kinetic properties similar to AtIAMT1 and poplar IAMT (PtIAMT1). Structural modeling of OsIAMT1 and PtIAMT1 using the experimentally determined structure of AtIAMT1 reported here as a template revealed conserved structural features of IAMTs within the active-site cavity that are divergent from functionally distinct members of the SABATH family, such as CbSAMT. Phylogenetic analysis revealed that IAMTs from Arabidopsis, rice, and poplar (Populus spp.) form a monophyletic group. Thus, structural, biochemical, and phylogenetic evidence supports the hypothesis that IAMT is an evolutionarily ancient member of the SABATH family likely to play a critical role in IAA homeostasis across a wide range of plants.
机译:植物SABATH蛋白家族包括一组相关的小分子甲基转移酶(MTs),它们催化天然化学物质的S-腺苷-1-甲硫氨酸依赖性甲基化,所述甲基化包含广泛不同的结构。吲哚-3-乙酸(IAA)甲基转移酶(IAMT)是SABATH家族的成员,它通过IAA的游离羧基甲基化来调节植物组织中的IAA稳态。测定拟南芥(Arabidopsis thaliana)IAMT(AtIAMT1)的晶体结构,并将其提纯至2.75Å分辨率。整体的三级和四级结构分别类似于两域双叶状单体和二聚体排列,先前已观察到来自Clarkia Breweri(CbSAMT)的相关水杨酸羧基甲基转移酶。为了进一步了解SABATH(尤其是IAMT)的生物学功能和进化,我们分析了水稻(Oryza sativa)基因组中的SABATH基因家族。鉴定出41个OsSABATH基因。表达分析表明,超过一半的OsSABATH基因在一个或多个器官中转录。与AtIAMT1最相似的OsSABATH基因是OsSABATH4。大肠杆菌表达的OsSABATH4蛋白显示出对IAA的最高催化活性,因此被命名为OsIAMT1。 OsIAMT1具有与AtIAMT1和杨树IAMT(PtIAMT1)相似的动力学特性。 OsIAMT1和PtIAMT1的结构建模使用此处确定的AtIAMT1实验确定的结构作为模板,揭示了活性位腔内IAMT的保守结构特征,这些结构特征与SABATH家族的功能不同成员(例如CbSAMT)不同。系统发育分析表明,来自拟南芥,水稻和杨树(Populus spp。)的IAMTs组成一个单系统群体。因此,结构,生化和系统发育证据支持以下假设:IAMT是SABATH家族的进化古老成员,可能在多种植物的IAA稳态中发挥关键作用。

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