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Mutation of OsLPR3 Enhances Tolerance to Phosphate Starvation in Rice
Monday, 2023/02/06 | 08:09:11

Hao Ai et al.

Int. J. Mol. Sci. 2023, 24(3), 2437; https://doi.org/10.3390/ijms24032437

 

Abstract

Low Phosphate Root (LPR) encodes a protein localized to the endoplasmic reticulum (ER) and cell wall. This gene plays a key role in responding to phosphate (Pi) deprivation, especially in remodeling the root system architecture (RSA). An identification and expression analysis of the OsLPR family in rice (Oryza sativa) has been previously reported, and OsLPR5, functioning in Pi uptake and translocation, is required for the normal growth and development of rice. However, the role of OsLPR3, one of the five members of this family in rice, in response to Pi deficiency and/or in the regulation of plant growth and development is unknown. Therefore, in this study, the roles of OsLPR3 in these processes were investigated, and some functions were found to differ between OsLPR3 and OsLPR5OsLPR3 was found to be induced in the leaf blades, leaf sheaths, and roots under Pi deprivation. OsLPR3 overexpression strongly inhibited the growth and development of the rice but did not affect the Pi homeostasis of the plant. However, oslpr3 mutants improved RSA and Pi utilization, and they exhibited a higher tolerance to low Pi stress in rice. The agronomic traits of the oslpr3 mutants, such as 1000-grain weight and seed length, were stimulated under Pi-sufficient conditions, indicating that OsLPR3 plays roles different from those of OsLPR5 during plant growth and development, as well as in the maintenance of the Pi status of rice.

 

See https://www.mdpi.com/1422-0067/24/3/2437

 

Figure 1. Variable effects of nutrient deficiencies on OsLPR3 transcript levels. Wild-type rice (Nipponbare) seedlings (10-d-old) were grown for 7 d in complete nutrient solution (CK) or in nutrient solution lacking nitrogen (−N), phosphorus (−P), potassium (−K), magnesium (−Mg), or iron (−Fe). Relative OsLPR3 transcript levels of leaf blades (A), leaf sheaths (B), and root (C) samples were determined and compared with OsActin1 via qPCR. Values are means ± SE (n = 3). Different letters above the bars indicate significant differences in the relative OsLPR3 transcript levels (p < 0.05, one-way ANOVA).

 

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