Zhu Jin-Qi, Zhang Jian-Tao, Tang Ren-Jie, Lv Qun-Dan, Wang Qiu-Qing, Yang Lei, Zhang Hong-Xia
National Key Laboratory of Plant Molecular Genetics, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, China.
Physiol Plant. 2009 Aug;136(4):407-25. doi: 10.1111/j.1399-3054.2009.01235.x. Epub 2009 May 19.
Inositol polyphosphate kinases play important roles in diverse cellular processes. In this study, the function of an inositol polyphosphate kinase gene homolog named ThIPK2 from a dicotyledonous halophyte Thellungiella halophila was investigated. The deduced translation product (ThIPK2) shares 85% identity with the Arabidopsis inositol polyphosphate kinase AtIPK2beta. Transient expression of ThIPK2-YFP fusion protein in tobacco (Nicotiana tabacum) protoplasts indicates that the protein is localized to the nucleus and plasma membrane, with a minor localization to the cytosol. Heterologous expression of ThIPK2 in ipk2Delta (also known as arg82Delta), a yeast mutant strain that lacks inositol polyphosphate multikinase (Ipk2) activity, rescued the mutant's salt-, osmotic- and temperature-sensitive growth defects. Semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) revealed ubiquitous expression of ThIPK2 in various tissues, including roots, rosette leaves, cauline leaves, stem, flowers and siliques, and shoot ThIPK2 transcript was strongly induced by NaCl or mannitol in T. halophila as exhibited by real-time PCR analysis. Transgenic expression of ThIPK2 in Brassica napus led to significantly improved salt-, dehydration- and oxidative stress resistance. Furthermore, the transcripts of various stress responsive marker genes increased in ThIPK2 transgenic plants under salt stress condition. These results suggest that ThIPK2 is involved in plant stress responses, and for the first time demonstrate that ThIPK2 could be a useful candidate gene for improving drought and salt tolerance in important crop plants by genetic transformation.
肌醇多磷酸激酶在多种细胞过程中发挥重要作用。在本研究中,对一种来自双子叶盐生植物盐芥的肌醇多磷酸激酶基因同源物ThIPK2的功能进行了研究。推导的翻译产物(ThIPK2)与拟南芥肌醇多磷酸激酶AtIPK2β具有85%的同一性。ThIPK2-YFP融合蛋白在烟草(Nicotiana tabacum)原生质体中的瞬时表达表明,该蛋白定位于细胞核和质膜,少量定位于细胞质溶胶。ThIPK2在缺乏肌醇多磷酸多激酶(Ipk2)活性的酵母突变株ipk2Delta(也称为arg82Delta)中的异源表达挽救了该突变体对盐、渗透和温度敏感的生长缺陷。半定量逆转录聚合酶链反应(RT-PCR)显示ThIPK2在包括根、莲座叶、茎生叶、茎、花和角果在内的各种组织中普遍表达,实时PCR分析表明,盐芥地上部分的ThIPK2转录本在NaCl或甘露醇处理下强烈诱导。ThIPK2在甘蓝型油菜中的转基因表达导致其对盐、脱水和氧化胁迫的抗性显著提高。此外,在盐胁迫条件下,ThIPK2转基因植物中各种胁迫响应标记基因的转录本增加。这些结果表明ThIPK2参与植物胁迫反应,并首次证明ThIPK2可能是通过遗传转化提高重要农作物耐旱性和耐盐性的有用候选基因。