State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, College of Horticulture, Nanjing Agricultural University, Nanjing 210095, China.
Genes (Basel). 2024 Jun 21;15(7):825. doi: 10.3390/genes15070825.
Yellowing leaves are ideal materials for studying the metabolic pathways of photosynthetic pigment chloroplast development, and the mechanism of photosynthetic systems. Here, we obtained a triploid material HCC (2n = 3x = 26), which was derived from hybridization between the artificial tetraploid × (2n = 4x = 38, HHCC) and the cultivated cucumber (2n = 2x = 14, CC), and this triploid HCC showed obvious leaf yellowing characteristics. Phenotypic observation results showed that chloroplast development was impaired, the chlorophyll content decreased, and photosynthesis decreased in yellowing HCC leaves. The transcriptome results indicated that HCC-GLK is significantly downregulated in HCC and participates in the regulation of leaf yellowing. GO enrichment analysis revealed that differential genes were enriched in the heme binding and tetrapyrrole binding pathways related to leaf color. KEGG enrichment analysis revealed that differential genes were predominantly enriched in photosynthesis-related pathways. The experimental results of VIGS and yeast hybridization showed that silencing the gene can induce leaf yellowing in cucumber plants, and the GLK protein can affect plant chloroplast development by interacting with the CAB3C protein (light-harvesting chlorophyll a/b binding) in the plant chlorophyll synthesis pathway. The current findings have not only enhanced our understanding of the regulatory mechanism of the GLK transcription factor in cucumber but also introduced novel insights and directions for investigating the molecular mechanism underlying polyploid leaf yellowing.
叶片发黄是研究光合作用色素叶绿体发育和光合系统代谢途径的理想材料。在这里,我们获得了一个三倍体材料 HCC(2n = 3x = 26),它是通过人工四倍体 × (2n = 4x = 38,HHCC)和栽培黄瓜 (2n = 2x = 14,CC)之间的杂交产生的,这个三倍体 HCC 表现出明显的叶片发黄特征。表型观察结果表明,叶绿体发育受损,叶绿素含量降低,发黄 HCC 叶片的光合作用降低。转录组结果表明,HCC-GLK 在 HCC 中显著下调,参与叶片发黄的调控。GO 富集分析表明,差异基因富集在与叶片颜色相关的血红素结合和四吡咯结合途径中。KEGG 富集分析表明,差异基因主要富集在光合作用相关途径中。VIGS 和酵母杂交的实验结果表明,沉默 基因可以诱导黄瓜植株叶片发黄,GLK 蛋白可以通过与植物叶绿素合成途径中的 CAB3C 蛋白(捕光叶绿素 a/b 结合)相互作用来影响植物叶绿体的发育。目前的研究结果不仅增强了我们对黄瓜 GLK 转录因子调控机制的理解,也为研究多倍体叶片发黄的分子机制提供了新的思路和方向。