State Key Laboratory of Crop Stress Biology for Arid Areas, College of Agronomy, Northwest A&F University, Yangling, Shaanxi 712100, China.
Department of Botany, The University of British Columbia, Vancouver, British Columbia, V6T 1Z4 Canada.
Plant Physiol. 2022 Oct 27;190(3):1640-1657. doi: 10.1093/plphys/kiac394.
Cuticular waxes cover the aerial surfaces of land plants and protect them from various environmental stresses. Alkanes are major wax components and contribute to plant drought tolerance, but the biosynthesis and regulation of alkanes remain largely unknown in wheat (Triticum aestivum L.). Here, we identified and functionally characterized a key alkane biosynthesis gene ECERIFERUM1-6A (TaCER1-6A) from wheat. The clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 (Cas9)-mediated knockout mutation in TaCER1-6A greatly reduced the contents of C27, C29, C31, and C33 alkanes in wheat leaves, while TaCER1-6A overexpression significantly increased the contents of these alkanes in wheat leaves, suggesting that TaCER1-6A is specifically involved in the biosynthesis of C27, C29, C31, and C33 alkanes on wheat leaf surfaces. TaCER1-6A knockout lines exhibited increased cuticle permeability and reduced drought tolerance, whereas TaCER1-6A overexpression lines displayed reduced cuticle permeability and enhanced drought tolerance. TaCER1-6A was highly expressed in flag leaf blades and seedling leaf blades and could respond to abiotic stresses and abscisic acid. TaCER1-6A was located in the endoplasmic reticulum, which is the subcellular compartment responsible for wax biosynthesis. A total of three haplotypes (HapI/II/III) of TaCER1-6A were identified in 43 wheat accessions, and HapI was the dominant haplotype (95%) in these wheat varieties. Additionally, we identified two R2R3-MYB transcription factors TaMYB96-2D and TaMYB96-5D that bound directly to the conserved motif CAACCA in promoters of the cuticular wax biosynthesis genes TaCER1-6A, TaCER1-1A, and fatty acyl-CoA reductase4. Collectively, these results suggest that TaCER1-6A is required for C27, C29, C31, and C33 alkanes biosynthesis and improves drought tolerance in wheat.
角质层蜡质覆盖在陆地植物的气生表面,保护它们免受各种环境胁迫。烷烃是蜡质的主要成分,有助于植物抗旱,但在小麦(Triticum aestivum L.)中,烷烃的生物合成和调控仍知之甚少。在这里,我们从小麦中鉴定并功能表征了一个关键的烷烃生物合成基因 ECERIFERUM1-6A(TaCER1-6A)。通过聚类规则间隔短回文重复序列(CRISPR)/CRISPR 相关蛋白 9(Cas9)介导的 TaCER1-6A 敲除突变,极大地降低了小麦叶片中 C27、C29、C31 和 C33 烷烃的含量,而 TaCER1-6A 过表达则显著增加了小麦叶片中这些烷烃的含量,这表明 TaCER1-6A 特异性地参与了小麦叶片表面 C27、C29、C31 和 C33 烷烃的生物合成。TaCER1-6A 敲除系表现出增加的角质层渗透率和降低的耐旱性,而 TaCER1-6A 过表达系则表现出降低的角质层渗透率和增强的耐旱性。TaCER1-6A 在旗叶和幼苗叶片中高表达,并能响应非生物胁迫和脱落酸。TaCER1-6A 位于内质网中,内质网是负责蜡质生物合成的亚细胞区室。在 43 个小麦品种中鉴定出 TaCER1-6A 的三种单倍型(HapI/II/III),其中 HapI 是这些小麦品种中的主要单倍型(95%)。此外,我们还鉴定出两个 R2R3-MYB 转录因子 TaMYB96-2D 和 TaMYB96-5D,它们直接结合到角质层蜡质生物合成基因 TaCER1-6A、TaCER1-1A 和脂肪酰基辅酶 A 还原酶 4 的启动子中的保守基序 CAACCA 上。总的来说,这些结果表明 TaCER1-6A 是 C27、C29、C31 和 C33 烷烃生物合成所必需的,并提高了小麦的耐旱性。