State Key Laboratory of Crop Stress Biology for Arid Areas, Northwest A&F University, Yangling, Shaanxi, 712100, China.
College of Agronomy, Northwest A&F University, Yangling, Shaanxi, 712100, China.
BMC Plant Biol. 2018 Mar 5;18(1):41. doi: 10.1186/s12870-018-1256-y.
The cuticle covers the surface of the polysaccharide cell wall of leaf epidermal cells and forms an essential diffusion barrier between the plant and the environment. The cuticle is composed of cutin and wax. Cuticular wax plays an important role in the survival of plants by serving as the interface between plants and their biotic and abiotic environments, especially restricting nonstomatal water loss. Leaf cuticular waxes of hexaploid wheat at the seedling stage mainly consist of primary alcohols, aldehydes, fatty acids, alkane and esters. Primary alcohols account for more than 80% of the total wax load. Therefore, we cloned several genes encoding fatty acyl-coenzyme A reductases from wheat and analyzed their function in yeast and plants. We propose the potential use of these genes in wheat genetic breeding.
We reported the cloning and characterization of three TaFARs, namely TaFAR6, TaFAR7 and TaFAR8, encoding fatty acyl-coenzyme A reductases (FAR) in wheat leaf cuticle. Expression analysis revealed that TaFAR6, TaFAR7 and TaFAR8 were expressed at the higher levels in the seedling leaf blades, and were expressed moderately or weakly in stamen, glumes, peduncle, flag leaf blade, sheath, spike, and pistil. The heterologous expression of three TaFARs in yeast (Saccharomyces cerevisiae) led to the production of C24:0 and C26:0 primary alcohols. Transgenic expression of the three TaFARs in tomato (Solanum lycopersicum) and rice (Oryza sativa) led to increased accumulation of C24:0-C30:0 primary alcohols. Transient expression of GFP protein-tagged TaFARs revealed that the three TaFAR proteins were localized to the endoplasmic reticulum (ER), the site of wax biosynthesis. The three TaFAR genes were transcriptionally induced by drought, cold, heat, powdery mildew (Blumeria graminis) infection, abscisic acid (ABA) and methyl jasmonate (MeJa) treatments.
These results indicated that wheat TaFAR6, TaFAR7 and TaFAR8 are involved in biosynthesis of very-long-chain primary alcohols in hexaploid wheat and in response to multiple environmental stresses.
表皮细胞的多糖细胞壁被角质层覆盖,形成植物与环境之间的必要扩散屏障。角质层由角鲨烯和蜡质组成。蜡质作为植物与其生物和非生物环境之间的界面,对植物的生存起着重要作用,特别是限制非气孔水分流失。六倍体小麦幼苗叶片的角质层蜡主要由伯醇、醛、脂肪酸、烷烃和酯组成。伯醇占总蜡负荷的 80%以上。因此,我们从小麦中克隆了几个编码脂肪酸辅酶 A 还原酶的基因,并在酵母和植物中分析了它们的功能。我们提出了这些基因在小麦遗传育种中的潜在应用。
我们报道了三个 TaFARs(TaFAR6、TaFAR7 和 TaFAR8)的克隆和特征,它们编码小麦叶片角质层中的脂肪酸辅酶 A 还原酶(FAR)。表达分析表明,TaFAR6、TaFAR7 和 TaFAR8 在幼苗叶片中表达水平较高,在雄蕊、颖片、花梗、旗叶、叶鞘、穗和雌蕊中表达水平中等或较弱。三个 TaFARs 在酵母(酿酒酵母)中的异源表达导致产生 C24:0 和 C26:0 伯醇。三个 TaFARs 在番茄(Solanum lycopersicum)和水稻(Oryza sativa)中的转基因表达导致 C24:0-C30:0 伯醇积累增加。GFP 蛋白标记的 TaFARs 的瞬时表达表明,这三种 TaFAR 蛋白定位于蜡质生物合成的内质网(ER)。干旱、寒冷、高温、白粉病(Blumeria graminis)感染、脱落酸(ABA)和茉莉酸甲酯(MeJa)处理诱导三个 TaFAR 基因的转录。
这些结果表明,小麦 TaFAR6、TaFAR7 和 TaFAR8 参与了六倍体小麦中非常长链伯醇的生物合成,并对多种环境胁迫作出反应。