Unidad de Recursos Genéticos, Instituto de Investigaciones Agropecuarias, INIA-Quilamapu, Chillán, Chile.
Plant Mol Biol. 2013 Jul;82(4-5):485-501. doi: 10.1007/s11103-013-0080-x. Epub 2013 Jun 4.
The cuticle is the first defense against pathogens and the second way water is lost in plants. Hydrophobic layers covering aerial plant organs from primary stages of development form cuticle, including major classes of aliphatic wax components and cutin. Extensive research has been conducted to understand cuticle formation mechanisms in plants. However, many questions remain unresolved in the transport of lipid components to form cuticle. Database studies of the Lotus japonicus genome have revealed the presence of 24 sequences classified as putative non-specific lipid transfer proteins (nsLTPs), which were classified in seven groups; four groups were selected because of their expression in aerial organs. LjLTP8 forms a cluster with DIR1 in Arabidopsis thaliana while LjLTP6, LjLTP9, and LjLTP10 were grouped as type I LTPs. In silico studies showed a high level of structural conservation, and substrate affinity studies revealed palmitoyl-CoA as the most likely ligand for these LTPs, although the Lyso-Myristoyl Phosphatidyl Choline, Lyso-myristoyl phosphatidyl glycerol, and Lyso-stearyl phosphatidyl choline ligands also showed a high affinity with the proteins. The LjLTP6 and LjLTP10 genes were expressed in both the stems and the leaves under normal conditions and were highly induced during drought stress. LjLTP10 was the most induced gene in shoots during drought. The gene was only expressed in the epidermal cells of stems, primordial leaves, and young leaflets. LjLTP10 was positively regulated by MeJA but repressed by abscisic acid (ABA), ethylene, and H2O2, while LjLTP6 was weakly induced by MeJA, repressed by H2O2, and not affected by ABA and ethylene. We suggest that LjLTP10 is involved in plant development of stem and leaf cuticle, but also in acclimation to tolerate drought stress in L. japonicus.
表皮是抵御病原体的第一道防线,也是植物水分流失的第二途径。从初级发育阶段开始,覆盖气生植物器官的疏水层形成表皮,包括主要类别的脂肪蜡成分和角质。人们已经进行了广泛的研究来了解植物表皮形成的机制。然而,在脂质成分向表皮的运输过程中,仍有许多问题尚未解决。对大豆基因组数据库的研究揭示了 24 个序列被归类为假定的非特异性脂质转移蛋白(nsLTPs),它们被分为 7 个组;由于它们在气生器官中的表达,选择了其中的 4 个组。LjLTP8 在拟南芥中与 DIR1 形成一个簇,而 LjLTP6、LjLTP9 和 LjLTP10 被归类为 I 型 LTPs。计算机研究表明,这些 LTPs 的结构高度保守,底物亲和力研究表明棕榈酰辅酶 A 是这些 LTPs 最有可能的配体,尽管溶血-myristoyl 磷酸胆碱、溶血-myristoyl 磷酸甘油和溶血-stearyl 磷酸胆碱配体与这些蛋白质也表现出很高的亲和力。LjLTP6 和 LjLTP10 基因在正常条件下在茎和叶中表达,在干旱胁迫下高度诱导。LjLTP10 是干旱胁迫下芽中诱导程度最高的基因。该基因仅在茎的表皮细胞、原基叶和幼叶中表达。LjLTP10 受 MeJA 正向调控,但受 ABA、乙烯和 H2O2 抑制,而 LjLTP6 受 MeJA 弱诱导,受 H2O2 抑制,不受 ABA 和乙烯影响。我们认为 LjLTP10 参与了茎和叶表皮的植物发育,但也参与了对大豆适应干旱胁迫的调节。