No abstract

OVATE gene was first identified as a key regulator of fruit shape in tomato. OVATE family proteins (OFPs) are characterized as plant-specific transcription factors and conserved in Arabidopsis, tomato, and rice. Roles of OFPs involved in plant development and growth are largely unknown. Brassinosteroids (BRs) are a class of steroid hormones involved in diverse biological functions. OsGKS2 plays a critical role in BR signaling by phosphorylating downstream components such as OsBZR1 and DLT. Here we report in rice that OsOFP8 plays a positive role in BR signaling pathway. BL treatment induced the expression of OsOFP8 and led to enhanced accumulation of OsOFP8 protein. The gain-of-function mutant Osofp8 and OsOFP8 overexpression lines showed enhanced lamina joint inclination, whereas OsOFP8 RNAi transgenic lines showed more upright leaf phenotype, which suggest that OsOFP8 is involved in BR responses. Further analyses indicated that OsGSK2 interacts with and phosphorylates OsOFP8. BRZ treatment resulted in the cytoplasmic distribution of OsOFP8, and bikinin treatment reduced the cytoplasmic accumulation of OsOFP8. Phosphorylation of OsOFP8 by OsGSK2 is needed for its nuclear export. The phospphorylated OsOFP8 shuttles to the cytoplasm and is targeted for proteasomal degradation. These results indicate that OsOFP8 is a substrate of OsGSK2 and the function of OsOFP8 in plant growth and development is at least partly through the BR signaling pathway.

Characterization of OVATE family proteins (OFPs) has revealed that they exert functions by interacting with different types of transcription factor. However, the molecular bases of these processes are poorly understood. Here, we report that OsOFP19 negatively modulates brassinosteroid (BR) response and integrates it with the cell division pattern to affect plant architecture, including grain shape, through interaction with both DWARF AND LOW-TILLERING (DLT) and Oryza sativa homeobox1 (OSH1). Overexpression of OsOFP19 caused a semi-dwarf stature with thicker leaves and stronger culms and roots, which result from an increase in cell layers in the sub-epidermal tissue. Further studies revealed that OsOFP19 interacts with OSH1, and that this interaction mutually enhances the transcriptional activity of these proteins and leads to a transition from anticlinal to periclinal cell division. Furthermore, DLT interacts with both OsOFP19 and OSH1 and acts as an antagonist in the two interactions. Therefore, OsOFP19, OSH1 and DLT form a functional complex which plays a pivotal role in modulating BR signaling and determining the cell division pattern during plant growth and development.

Plants transport photoassimilates from source organs to sink tissues through the phloem translocation pathway. In the transport phloem, sugars that escape from the sieve tubes are released into the apoplasmic space between the sieve element/companion cell complex (SE/CC) and phloem parenchyma cells (PPCs) during the process of long-distance transport. The competition for sugar acquisition between SE/CC and adjoining PPCs is mediated by plasma membrane translocators. YFP-tagged AtSWEET4 protein is localized in the plasma membrane, and PromoterAtSWEET4-GUS analysis showed that AtSWEET4 is expressed in the stele of roots and veins of leaves and flowers. Overexpression of AtSWEET4 in Arabidopsis increases plant size and accumulates more glucose and fructose. By contrast, knock-down of AtSWEET4 by RNA-interference leads to small plant size, reduction in glucose and fructose contents, chlorosis in the leaf vein network, and reduction in chlorophyll content in leaves. Yeast assays demonstrated that AtSWEET4 is able to complement both fructose and glucose transport deficiency. Transgenic plants of AtSWEET4 overexpression exhibit higher freezing tolerance and support more growth of bacterium Pseudomonas syringae pv. phaseolicola NPS3121. We conclude that AtSWEET4 plays an important role in mediating sugar transport in axial tissues during plant growth and development.

The effects of graphene on the germination and growth of rice seeds were studied. Seeds were treated with graphene solutions at different concentrations. Obvious delaying effects on the germination rate were observed with the increasing of graphene concentration. The growth of radicle and plumule was inhibited. And also, the morphology (root length, stem length, adventitious number, root fresh weight, fresh weight of over ground part and root cap ratio) of rice seedlings was certainly affected. After been treated by different concentrations of graphene for 16 d, promoting effects on adventitious root number, root fresh weight and fresh weight of over ground part were observed at concentration of 5 mg/L. Significant inhibitions on the stem length and fresh weight of over ground part were observed at concentration of 50 mg/L. In addition, all the indexes were inhibited at concentrations of 100 mg/L and 200 mg/L. It indicates that graphene certainly inhibit the morphogenesis of rice seedlings. But the mechanism by which graphene of 5 mg/L improves part of growth indexes still needs further study.