Yang Mailun, Sakuraba Yasuhito, Yanagisawa Shuichi
Agro-Biotechnology Research Center, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan.
J Exp Bot. 2025 Jan 10;76(2):461-477. doi: 10.1093/jxb/erae440.
Rice HRS1 HOMOLOG3 (OsHHO3) acts as a transcriptional repressor of AMMONIUM TRANSPORTER1 (OsAMT1) genes in rice; thus, reduced OsHHO3 expression in nitrogen (N)-deficient environments promotes ammonium uptake. In this study, we show that OsHHO3 also functions as a repressor of a specific subset of phosphate (Pi) transporter (PT) genes involved in the uptake and root-to-shoot translocation of Pi, including OsPT2, OsPT4, and OsPHO1;1. Disruption of OsHHO3 increased Pi uptake and Pi contents in shoots and roots, while overexpression of OsHHO3 caused the opposite effects. Furthermore, phosphorus (P) deficiency slightly decreased OsHHO3 expression, up-regulating a specific subset of PT genes. However, N deficiency was more effective than P deficiency in suppressing OsHHO3 expression in roots, and unlike N deficiency-dependent activation of PT genes under the control of OsHHO3, the P deficiency-dependent activation of OsAMT1 genes was minimal. Interestingly, the simultaneous deficiency of both N and P promoted the OsHHO3-regulated expression of PT genes more significantly than the deficiency of either N or P, but diminished the expression of genes regulated by OsPHR2, a master regulator of Pi starvation-responsive transcriptional activation. Phenotypic analysis revealed that the inactivation and overexpression of OsHHO3 improved and reduced plant growth, respectively, under N-deficient and P-deficient conditions. These results indicate that OsHHO3 regulates a specific subset of PT genes independently of OsPHR2-mediated regulation and plays a critical role in the adaptation to diverse N and P environments.
水稻HRS1同源物3(OsHHO3)作为水稻铵转运蛋白1(OsAMT1)基因的转录抑制因子;因此,在缺氮环境中OsHHO3表达降低会促进铵的吸收。在本研究中,我们发现OsHHO3还作为参与磷(Pi)吸收和从根到地上部转运的特定Pi转运蛋白(PT)基因子集的抑制因子,包括OsPT2、OsPT4和OsPHO1;1。OsHHO3的破坏增加了地上部和根部的Pi吸收及Pi含量,而OsHHO3的过表达则产生相反的效果。此外,缺磷会轻微降低OsHHO3的表达,上调特定的PT基因子集。然而,缺氮比缺磷更有效地抑制根中OsHHO3的表达,并且与在OsHHO3控制下缺氮依赖性激活PT基因不同,缺磷依赖性激活OsAMT1基因的作用最小。有趣的是,氮磷同时缺乏比单独缺氮或缺磷更显著地促进了OsHHO3调控的PT基因表达,但减少了由Pi饥饿响应转录激活的主要调节因子OsPHR2调控的基因表达。表型分析表明,在缺氮和缺磷条件下,OsHHO3的失活和过表达分别改善和降低了植物生长。这些结果表明,OsHHO3独立于OsPHR2介导的调控来调节特定的PT基因子集,并在适应不同的氮磷环境中起关键作用。