Rice (
Oryza sativa L.), a globally staple food crop, frequently encounters growth, developmental, and yield limitations due to phosphate deficiency.
LOW PHOSPHATE ROOT1/
2 (
LPR1/
2) are essential genes in plants that regulate primary root growth and respond
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Rice (
Oryza sativa L.), a globally staple food crop, frequently encounters growth, developmental, and yield limitations due to phosphate deficiency.
LOW PHOSPHATE ROOT1/
2 (
LPR1/
2) are essential genes in plants that regulate primary root growth and respond to local phosphate deficiency signals under low phosphate stress. In rice, five
LPR genes, designated
OsLPR1–
OsLPR5 based on their sequence identity with
AtLPR1, have been identified.
OsLPR3 and
OsLPR5 are specifically expressed in roots and induced by phosphate deficiency, contributing to rice growth, development, and the maintenance of phosphorus homeostasis under low phosphate stress. In contrast,
OsLPR2 is uniquely expressed in shoots, suggesting it may have distinct functions compared with other family members. This study employed Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated protein 9 (CRISPR/Cas9) gene editing technology to generate
oslpr2 mutant transgenic lines and subsequently investigated the effect of
OsLPR2 gene knockout on rice growth, phosphate utilization, and salt stress tolerance in the seedling stage, as well as the effect of
OsLPR2 gene knockout on rice development and agronomic traits in the maturation stage. The results indicated that the knockout of
OsLPR2 did not significantly impact rice seedling growth or phosphate utilization, which contrasts significantly with its homologous genes,
OsLPR3 and
OsLPR5. However, the mutation influenced various agronomic traits at maturity, including plant height, tiller number, and seed setting rate. Moreover, the
OsLPR2 mutation conferred enhanced salt stress tolerance in rice. These findings underscore the distinct roles of
OsLPR2 compared with other homologous genes, establishing a foundation for further investigation into the function of the
OsLPR family and the functional differentiation among its members.
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