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蓖麻(Ricinus communis L.)种子中编码肌醇1,3,4,5,6 - 五磷酸2 - 激酶的mRNA变体的分子和生化鉴定

Molecular and biochemical identification of inositol 1,3,4,5,6-pentakisphosphate 2-kinase encoding mRNA variants in castor bean (Ricinus communis L.) seeds.

作者信息

Yu Jaeju, Saiardi Adolfo, Greenwood John S, Bewley J Derek

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, N1G 2W1, Canada.

出版信息

Planta. 2014 May;239(5):965-77. doi: 10.1007/s00425-014-2028-z. Epub 2014 Jan 25.

Abstract

During seed development, phytic acid (PA) associated with mineral cations is stored as phytin and mobilized following germination in support of seedling growth. Two parallel biosynthetic pathways for PA have been proposed; yet the pathway is still poorly understood in terms of its regulation and the enzymes involved. Here, the castor bean (Ricinus communis L.) gene for inositol 1,3,4,5,6-pentakisphosphate 2-kinase (RcIPK1) has been identified. This encodes the enzyme implicated in catalyzing the final reaction in PA biosynthesis, and its expression is enhanced in isolated germinated embryos by application of phosphate and myo-inositol (Ins). Even though only one copy of the RcIPK1 gene is present in the genome, numerous RNA variants are present, most likely due to alternative splicing. These are translated into six closely related protein isoforms according to in silico analysis. Functional analyses using yeast ipk1Δ revealed that only three of the mRNA variants can rescue a temperature-sensitive growth phenotype of this strain. High-performance liquid chromatography (HPLC) analysis of the synthesized inositol phosphates demonstrated that the ability to complement the missing yeast IPK1 enzyme is associated with the production of enzyme activity. The three active isoforms possess unique conserved motifs important for IPK1 catalytic activity.

摘要

在种子发育过程中,与矿质阳离子结合的植酸(PA)以肌醇六磷酸的形式储存,并在种子萌发后被调动以支持幼苗生长。已经提出了两条平行的PA生物合成途径;然而,就其调控和所涉及的酶而言,该途径仍未得到充分理解。在此,已鉴定出蓖麻(Ricinus communis L.)的肌醇1,3,4,5,6 - 五磷酸2 - 激酶(RcIPK1)基因。该基因编码参与催化PA生物合成中最后一步反应的酶,并且通过施加磷酸盐和肌醇(Ins),其在分离的萌发胚中的表达增强。尽管基因组中仅存在一个RcIPK1基因拷贝,但存在大量RNA变体,这很可能是由于可变剪接所致。根据计算机分析,这些RNA变体被翻译成六种密切相关的蛋白质异构体。使用酵母ipk1Δ进行的功能分析表明,只有三种mRNA变体能够挽救该菌株的温度敏感型生长表型。对合成的肌醇磷酸进行的高效液相色谱(HPLC)分析表明,补充缺失的酵母IPK1酶的能力与酶活性的产生相关。这三种活性异构体具有对IPK1催化活性重要的独特保守基序。

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