Kumar Suresh, Agrawal Anuradha, Seem Karishma, Kumar Santosh, Vinod K K, Mohapatra Trilochan
Division of Biochemistry, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Decode Genomics Private Limited, New Delhi, India.
Plant Mol Biol. 2022 May;109(1-2):29-50. doi: 10.1007/s11103-022-01254-z. Epub 2022 Mar 11.
Phosphorus (P) is essential for cellular processes like respiration, photosynthesis, biosynthesis of membrane phospholipids, etc. To cope with P deficiency stress, plants adopt reprograming of the expression of genes involved in different metabolic/signaling pathways for survival, growth, and development. Plants use transcriptional, post-transcriptional, and/or post-translational machinery to achieve P homeostasis. Several transcription factors (TFs), miRNAs, and P transporters play important roles in P deficiency tolerance; however, the underlying mechanisms responsible for P deficiency tolerance remain poorly understood. Studies on P starvation/deficiency responses in plants at early (seedling) stage of growth have been reported but only a few of them focused on molecular responses of the plant at advanced (tillering or reproductive) stage of growth. To decipher the strategies adopted by rice at tillering stage under P deficiency stress, a pair of contrasting genotypes [Pusa-44 (a high-yielding, P deficiency sensitive cultivar) and its near-isogenic line (NIL-23, P deficiency tolerant) for Pup1 QTL] was used for morphophysiological, biochemical, and molecular analyses. Comparative analyses of shoot and root tissues from 45-day-old plants grown hydroponically under P sufficient (16 ppm) or P deficient (4 ppm) medium confirmed some of the known morphophysiological responses. Moreover, RNA-seq analysis revealed the important roles of phosphate transporters, TFs, auxin-responsive proteins, modulation in the cell wall, fatty acid metabolism, and chromatin architecture/epigenetic modifications in providing P deficiency tolerance to NIL-23, which were brought in due to the introgression of the Pup1 QTL in Pusa-44. This study provides insights into the molecular functions of Pup1 for P deficiency tolerance, which might be utilized to improve P-use efficiency of rice for better productivity in P deficient soils. KEY MESSAGE: Introgression of Pup1 QTL in high-yielding rice cultivar modulates mainly phosphate transporters, TFs, auxin-responsive proteins, cell wall structure, fatty acid metabolism, and chromatin architecture/epigenetic modifications at tillering stage of growth under phosphorus deficiency stress.
磷(P)对于细胞呼吸、光合作用、膜磷脂生物合成等细胞过程至关重要。为应对磷缺乏胁迫,植物通过重新编程参与不同代谢/信号通路的基因表达来实现生存、生长和发育。植物利用转录、转录后和/或翻译后机制来维持磷稳态。几种转录因子(TFs)、微小RNA(miRNAs)和磷转运蛋白在耐低磷性中发挥重要作用;然而,耐低磷性的潜在机制仍知之甚少。已有关于植物生长早期(幼苗期)对磷饥饿/缺乏响应的研究报道,但其中只有少数研究关注植物生长后期(分蘖期或生殖期)的分子响应。为了解水稻在分蘖期低磷胁迫下所采用的策略,使用了一对对比基因型[Pusa - 44(高产、低磷敏感品种)及其Pup1 QTL的近等基因系(NIL - 23,耐低磷)]进行形态生理、生化和分子分析。对水培在磷充足(16 ppm)或磷缺乏(4 ppm)培养基中的45日龄植株的地上部和根部组织进行比较分析,证实了一些已知的形态生理响应。此外,RNA测序分析揭示了磷酸盐转运蛋白、转录因子、生长素响应蛋白、细胞壁调节、脂肪酸代谢以及染色质结构/表观遗传修饰在赋予NIL - 23耐低磷性方面的重要作用,这是由于Pup1 QTL导入Pusa - 44所致。本研究深入了解了Pup1在耐低磷性方面的分子功能,这可能有助于提高水稻在低磷土壤中的磷利用效率,以实现更高的产量。关键信息:高产水稻品种中Pup1 QTL的导入主要调节了磷缺乏胁迫下分蘖期的磷酸盐转运蛋白、转录因子、生长素响应蛋白、细胞壁结构、脂肪酸代谢以及染色质结构/表观遗传修饰。