Agro-Biotechnology Research Center, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo, 113-8657, Japan.
New Phytol. 2024 Jun;242(5):2132-2147. doi: 10.1111/nph.19695. Epub 2024 Mar 24.
Elucidating the mechanisms regulating nitrogen (N) deficiency responses in plants is of great agricultural importance. Previous studies revealed that decreased expression of NITRATE-INDUCIBLE GARP-TYPE TRANSCRIPTIONAL REPRESSOR1 (NIGT1) transcriptional repressor genes upon N deficiency is involved in N deficiency-inducible gene expression in Arabidopsis thaliana. However, our knowledge of the mechanisms controlling N deficiency-induced changes in gene expression is still limited. Through the identification of Dof1.7 as a direct target of NIGT1 repressors and a novel N deficiency response-related transcriptional activator gene, we here show that NIGT1 and Dof1.7 transcription factors (TFs) differentially regulate N deficiency-inducible expression of three high-affinity nitrate transporter genes, NRT2.1, NRT2.4, and NRT2.5, which are responsible for most of the soil nitrate uptake activity of Arabidopsis plants under N-deficient conditions. Unlike NIGT1 repressors, which directly suppress NRT2.1, NRT2.4, and NRT2.5 under N-sufficient conditions, Dof1.7 directly activated only NRT2.5 but indirectly and moderately activated NRT2.1 and NRT2.4 under N-deficient conditions, probably by indirectly decreasing NIGT1 expression. Thus, Dof1.7 converted passive transcriptional activation into active and potent transcriptional activation, further differentially enhancing the expression of NRT2 genes. These findings clarify the mechanism underlying different expression patterns of NRT2 genes upon N deficiency, suggesting that time-dependent multilayered transcriptional regulation generates complicated expression patterns of N deficiency-inducible genes.
阐明植物氮(N)缺乏响应的调控机制具有重要的农业意义。先前的研究表明,拟南芥 N 缺乏诱导基因表达中,NITRATE-INDUCIBLE GARP-TYPE TRANSCRIPTIONAL REPRESSOR1(NIGT1)转录抑制基因表达下调涉及 N 缺乏诱导基因表达。然而,我们对控制 N 缺乏诱导基因表达变化的机制的认识仍然有限。通过鉴定 Dof1.7 作为 NIGT1 抑制剂的直接靶标和一个新的 N 缺乏反应相关转录激活因子基因,我们表明 NIGT1 和 Dof1.7 转录因子(TFs)差异调控三个高亲和力硝酸盐转运体基因(NRT2.1、NRT2.4 和 NRT2.5)的 N 缺乏诱导表达,这些基因负责拟南芥植物在 N 缺乏条件下大部分的土壤硝酸盐摄取活性。与 NIGT1 抑制剂在 N 充足条件下直接抑制 NRT2.1、NRT2.4 和 NRT2.5 不同,Dof1.7 仅在 N 缺乏条件下直接激活 NRT2.5,但间接且适度激活 NRT2.1 和 NRT2.4,可能通过间接降低 NIGT1 表达。因此,Dof1.7 将被动转录激活转化为主动和有力的转录激活,进一步差异增强 NRT2 基因的表达。这些发现阐明了 N 缺乏时 NRT2 基因不同表达模式的机制,表明时间依赖性多层转录调控产生了复杂的 N 缺乏诱导基因表达模式。