State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin 150040, China.
College of Life Science, Northeast Forestry University, Harbin 150040, China.
Int J Mol Sci. 2023 Sep 6;24(18):13748. doi: 10.3390/ijms241813748.
Roots are the main organ for water uptake and the earliest part of a plant's response to drought, making them of great importance to our understanding of the root system's response to drought. However, little is known about the underlying molecular mechanisms that control root responses to drought stress. Here, we identified and functionally characterized the AP2/ERF family transcription factor (TF) and the upstream target gene zinc-finger protein TF PtrYY1, which respond to drought stress by promoting the growth and development of lateral roots in . A root-specific induction of under drought stress was explored. The overexpression of () promoted root growth and development, thereby increasing tolerance to drought stress. In addition, PtrYY1 is directly bound to the promoter of under drought stress, and the overexpression of () promoted lateral root growth and development and increased tolerance to drought stress. An RNA-seq analysis of with wild-type (WT) poplar identified and , which share the same pattern of expression changes as . A qRT-PCR and cis-element analysis further suggested that and may act as potential downstream targets of PtrABR1 genes in the root response pathway to drought stress. In conclusion, these results reveal a novel drought regulatory pathway in which regulates the network through the upstream target gene PtrYY1 and the potential downstream target genes and , thereby promoting root growth and development and improving tolerance to drought stress.
根是植物吸收水分的主要器官,也是植物对干旱最早做出响应的部分,这使得它们对于我们理解根系对干旱的响应具有重要意义。然而,对于控制根响应干旱胁迫的潜在分子机制知之甚少。在这里,我们鉴定并功能表征了 AP2/ERF 家族转录因子(TF)和上游靶基因锌指蛋白 TF PtrYY1,它们通过促进侧根的生长和发育来响应干旱胁迫。探讨了干旱胁迫下 根特异性诱导。过量表达 ()促进了根的生长和发育,从而提高了对干旱胁迫的耐受性。此外,PtrYY1 在干旱胁迫下直接与 的启动子结合,过量表达 ()促进了侧根的生长和发育,提高了对干旱胁迫的耐受性。对与野生型(WT)杨树的 进行 RNA-seq 分析,鉴定了 和 ,它们的表达变化模式与 相同。qRT-PCR 和顺式元件分析进一步表明,和 可能作为干旱胁迫下根响应途径中 PtrABR1 基因的潜在下游靶标。总之,这些结果揭示了一个新的干旱调控途径,其中 通过上游靶基因 PtrYY1 以及潜在的下游靶基因 和 调节网络,从而促进根的生长和发育,提高对干旱胁迫的耐受性。