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Keywords: auxin signal; lamina joint; leaf angle; LIGULELESS 2s; LIGULELESS 1; organogenesis; Oryza sativa EN auxin signal lamina joint leaf angle LIGULELESS 2s LIGULELESS 1 organogenesis Oryza sativa 1832 1839 8 01/21/21 20210215 NES 210215 The lamina joint (LJ) is a grass-specific organ that connects the leaf blade to the sheath and causes the leaf blade to bend away from the vertical axis. Notably, the regulation of LJ differentiation by I OsLG1 i is dependent on the LJ position determination by I OsLG2 i and I OsLG2L i , because the LJ differentiation was absent in I OsLG2-cri;OsLG2L-cri i . I OsLG2 i and I OsLG2L i are essential for determining the LJ position; I OsLG1 i is necessary to initiate LJ differentiation, which depends on the LJ positioning determined by I OsLG2/2L i . [Extracted from the article]

Rice tillering, a key architecture trait determining grain yield, is highly regulated by a class of newly identified phytohormones, strigolactones (SLs). However, the whole SL signaling pathway from the receptor to downstream transcription factors to finally inhibit tillering remains unrevealed. In this study, we first found that brassinosteroids (BRs) strongly enhance tillering by promoting bud outgrowth in rice, which is largely different from the function of BRs in Arabidopsis. Genetic and biochemical analyses indicated that both the SL and BR signaling pathways control rice tillering by regulating the stability of D53 and/or the OsBZR1–RLA1–DLT module, a transcriptional complex in the rice BR signaling pathway. We further found that D53 interacts with OsBZR1 to inhibit the expression of FC1 , a local inhibitor of tillering, and that this inhibition depends on direct DNA binding by OsBZR1, which recruits D53 to the FC1 promoter in rice buds. Taken together, these findings uncover a mechanism illustrating how SLs and BRs coordinately regulate rice tillering via the early responsive gene FC1. This study reports that BRs play an important role in promoting rice tillering. It is shown that SLs and BRs antagonistically regulate rice tillering by regulating FC1 expression in rice buds, which depends on the D53–OsBZR1 complex, and that OsBZR1 directly binds the FC1 promoter and recruits D53 to inhibit FC1 expression. [ABSTRACT FROM AUTHOR]

Rice includes 93 nitrate and peptide transporters family (NPF) members that facilitate the soil uptake and internal reallocation of nitrogen for growth and development. This study demonstrated that OsNPF7.7 had two splicing variants, and altered expression of each variant could regulate shoot branching and nitrogen utilization efficiency (NUtE) in rice. The expression of both variants was down-regulated in the buds by increased nitrogen level in the Japonica rice variety ZH11. The expression level of long-variant OsNPF7.7-1 was higher in panicles at reproductive stage, however, the expression level of short-variant OsNPF7.7-2 was higher in buds and leaves at vegetative stage compared to each other in ZH11. OsNPF7.7-1 was localized in the plasma membrane, whereas OsNPF7.7-2 was localized in the vacuole membrane. Furthermore, the results indicated that the expression level of each variant for OsNPF7.7 determined axillary bud outgrowth, and then influenced the rice tiller number. Overexpression of OsNPF7.7-1 could promote nitrate influx and concentration in root, whereas overexpression of OsNPF7.7-2 could improve ammonium influx and concentration in root. RNAi and osnpf7.7 lines of OsNPF7.7 showed an increased amount of amino acids in leaf sheaths, but a decreased amount in leaf blades, which affected nitrogen allocation and plant growth. The elevated expression of each variant for OsNPF7.7 in ZH11 enhanced NUtE using certain fertilization regimes under paddy field conditions. Moreover, overexpression of each variant for OsNPF7.7 in KY131 increased significantly the filled grain number per plant. Thus, increased each variant of OsNPF7.7 has the potential to improve grain yield and NUtE in rice. [ABSTRACT FROM AUTHOR]

Brassinosteroids (BRs) are plant-specific steroid hormones that control plant growth and development. Recent studies have identified key components of the BR signaling pathway in Arabidopsis thaliana and in rice (Oryza sativa); however, the mechanism of BR signaling in rice, especially downstream of GSK3/SHAGGY-like kinase (GSK2), remains unclear. Here, we identified a BR-insensitive rice mutant, reduced leaf angle1 (rla1), and cloned the corresponding gene. RLA1 was identical to the previously reported SMALL ORGAN SIZE1 (SMOS1), which was cloned from another allele. RLA1/SMOS1 encodes a transcription factor with an APETALA2 DNA binding domain. Genetic analysis indicated that RLA1/SMOS1 functions as a positive regulator in the BR signaling pathway and is required for the function of BRASSINAZOLE-RESISTANT1 (OsBZR1). In addition, RLA1/SMOS1 can interact with OsBZR1 to enhance its transcriptional activity. GSK2 can interact with and phosphorylate RLA1/SMOS1 to reduce its stability. These results demonstrate that RLA1/SMOS1 acts as an integrator of the transcriptional complex directly downstream of GSK2 and plays an essential role in BR signaling and plant development in rice. [ABSTRACT FROM AUTHOR]

Summary Leaf erectness is key in determining plant architecture and yield, particularly in cereal crops. Brassinosteroids (BRs) play a unique role in controlling this trait in monocots, but the underlying cellular and molecular mechanisms remain big mysteries. Here we report that the abaxial sclerenchyma cell number of rice lamina joints (LJs) is closely related to leaf erectness, and BR signaling tightly regulates their proliferation. We identified a rice U-type cyclin CYC U4;1 enriched in rice LJs, with its expression accompanying LJ development. Genetic and biochemical studies demonstrated that CYC U4;1 plays a positive role in promoting leaf erectness by controlling the abaxial sclerenchyma cell proliferation. Furthermore, BR signaling inhibits the abaxial sclerenchyma cell division by coordinately regulating CYC U4;1 expression through BES1 and CYC U4;1 protein activity through GSK3 kinases. These results support a key role of the cyclin CYC U4;1 in mediating BR-regulated cell division to control leaf erectness. [ABSTRACT FROM AUTHOR]