López-Millán Ana-Flor, Ellis Danielle R, Grusak Michael A
Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, 1100 Bates Street, Houston, TX 77030, USA.
Plant Mol Biol. 2004 Mar;54(4):583-96. doi: 10.1023/B:PLAN.0000038271.96019.aa.
To broaden our understanding of micronutrient metal transport in plants, we have identified cDNAs for six new metal transporters in the model legume Medicago truncatula. All of the predicted proteins have high similarity to the ZIP protein family, and have been designated MtZIP1, MtZIP3, MtZIP4, MtZIP5, MtZIP6, and MtZIP7. The six predicted proteins ranged from 350 to 372 amino acids in length; sequence analysis revealed that all proteins contained eight transmembrane domains and the highly conserved ZIP signature motif. Most of the proteins also exhibited a histidine-rich region in the variable sequence between transmembrane domains III and IV. When MtZIPs were transformed into appropriate metal-uptake defective yeast mutants and grown on metal-limited media, MtZIP1, MtZIP5, and MtZIP6 proteins restored yeast growth on Zn-limited media, MtZIP4 and MtZIP7 proteins restored yeast growth on Mn-limited media, and MtZIP3, MtZIP5, and MtZIP6 proteins restored yeast growth on Fe-limited media. Therefore, we conclude that these proteins function as metal transporters in Medicago truncatula. The expression pattern for each gene was studied by semi-quantitative RT-PCR in roots and leaves from plants grown under various metal supplies. MtZIP1 transcripts were only detected in Zn-deficient roots and leaves. MtZIP3 and MtZIP4 expression was down regulated in leaves from Mn- and Fe-deficient plants and appeared to be upregulated under Zn-deficient conditions in both roots and leaves. MtZIP5 was upregulated in leaves under Zn and Mn deficiency. The expression of MtZIP6 and MtZIP7 was unaffected by the metal supply, at least in root and leaf tissues. Characterizing these proteins in a single organism will allow us to understand the interplay between various ZIP genes, and the role they play in the regulation/execution of plant metal homeostasis.
为了拓宽我们对植物中微量营养金属转运的理解,我们在模式豆科植物蒺藜苜蓿中鉴定出了六种新金属转运蛋白的cDNA。所有预测的蛋白质与ZIP蛋白家族具有高度相似性,并被命名为MtZIP1、MtZIP3、MtZIP4、MtZIP5、MtZIP6和MtZIP7。这六种预测的蛋白质长度在350至372个氨基酸之间;序列分析表明,所有蛋白质都包含八个跨膜结构域和高度保守的ZIP特征基序。大多数蛋白质在跨膜结构域III和IV之间的可变序列中还表现出富含组氨酸的区域。当将MtZIPs转化到合适的金属吸收缺陷型酵母突变体中,并在金属限制培养基上生长时,MtZIP1、MtZIP5和MtZIP6蛋白在锌限制培养基上恢复了酵母生长,MtZIP4和MtZIP7蛋白在锰限制培养基上恢复了酵母生长,MtZIP3、MtZIP5和MtZIP6蛋白在铁限制培养基上恢复了酵母生长。因此,我们得出结论,这些蛋白质在蒺藜苜蓿中作为金属转运蛋白发挥作用。通过半定量RT-PCR研究了在各种金属供应条件下生长的植物的根和叶中每个基因的表达模式。MtZIP1转录本仅在缺锌的根和叶中检测到。MtZIP3和MtZIP4的表达在缺锰和缺铁植物的叶中下调,并且在根和叶中缺锌条件下似乎上调。MtZIP5在锌和锰缺乏时在叶中上调。MtZIP6和MtZIP7的表达不受金属供应的影响,至少在根和叶组织中是这样。在单一生物体中对这些蛋白质进行表征将使我们能够了解各种ZIP基因之间的相互作用,以及它们在植物金属稳态调节/执行中所起的作用。