Tong Yiping, Zhou Jing-Jiang, Li Zhensheng, Miller Anthony J
Crop Performance and Improvement Division, Harpenden, Hertfordshire, AL5 2JQ, UK.
Plant J. 2005 Feb;41(3):442-50. doi: 10.1111/j.1365-313X.2004.02310.x.
The analysis of genome databases for many different plants has identified a group of genes that are related to one part of a two-component nitrate transport system found in algae. Earlier work using mutants and heterologous expression has shown that a high-affinity nitrate transport system from the unicellular green algae, Chlamydomonas reinhardtii required two gene products for function. One gene encoded a typical carrier-type structure with 12 putative trans-membrane (TM) domains and the other gene, nar2 encoded a much smaller protein that had only one TM domain. As both gene families occur in plants we investigated whether this transport model has more general relevance among plants. The screening for nitrate transporter activity was greatly helped by a novel assay using (15)N-enriched nitrate uptake into Xenopus oocytes expressing the proteins. This assay enables many oocytes to be rapidly screened for nitrate transport activity. The functional activity of a barley nitrate transporter, HvNRT2.1, in oocytes required co-injection of a second mRNA. Although three very closely related nar2-like genes were cloned from barley, only one of these was able to give functional nitrate transport when co-injected into oocytes. The nitrate transport performed by this two-gene system was inhibited at more acidic external pH and by acidification of the cytoplasm. This specific requirement for two-gene products to give nitrate transport function has important implications for attempts to genetically manipulate this fundamental process in plants.
对许多不同植物的基因组数据库进行分析后,已鉴定出一组与藻类中双组分硝酸盐转运系统的一部分相关的基因。早期利用突变体和异源表达进行的研究表明,单细胞绿藻莱茵衣藻中的高亲和力硝酸盐转运系统需要两种基因产物才能发挥功能。一个基因编码一种具有12个推定跨膜(TM)结构域的典型载体型结构,另一个基因nar2编码一种小得多的蛋白质,该蛋白质只有一个TM结构域。由于这两个基因家族都存在于植物中,我们研究了这种转运模式在植物中是否具有更广泛的相关性。一种使用将富集(15)N的硝酸盐摄取到表达这些蛋白质的非洲爪蟾卵母细胞中的新型检测方法,极大地有助于筛选硝酸盐转运蛋白活性。这种检测方法能够快速筛选许多卵母细胞的硝酸盐转运活性。大麦硝酸盐转运蛋白HvNRT2.1在卵母细胞中的功能活性需要共注射第二种mRNA。虽然从大麦中克隆出了三个非常密切相关的nar2样基因,但只有其中一个在共注射到卵母细胞中时能够产生功能性的硝酸盐转运。由这个双基因系统进行的硝酸盐转运在更酸性的外部pH值和细胞质酸化时受到抑制。对两种基因产物赋予硝酸盐转运功能的这种特定要求,对于在植物中对这一基本过程进行基因操作的尝试具有重要意义。