Wheat, an essential crop for global food security, is well adapted to a wide variety of soils. However, the gene networks shaping different root architectures remain poorly understood. We report here that dosage differences in a cluster of monocot-specific 12-OXOPHYTODIENOATE REDUCTASE genes from subfamily III (OPRIII) modulate key differences in wheat root architecture, which are associated with grain yield under water-limited conditions. Wheat plants with loss-of-function mutations in OPRIII show longer seminal roots, whereas increased OPRIII dosage or transgenic over-expression result in reduced seminal root growth, precocious development of lateral roots and increased jasmonic acid (JA and JA-Ile). Pharmacological inhibition of JA-biosynthesis abolishes root length differences, consistent with a JA-mediated mechanism. Transcriptome analyses of transgenic and wild-type lines show significant enriched JA-biosynthetic and reactive oxygen species (ROS) pathways, which parallel changes in ROS distribution. OPRIII genes provide a useful entry point to engineer root architecture in wheat and other cereals.

The introgression of a small segment of wheat (Triticum aestivum L.) chromosome arm 1BS in the distal region of the rye (Secale cereale L.) 1RS.1BL arm translocation in wheat (henceforth 1RS^RW) was previously associated with reduced grain yield, carbon isotope discrimination, and stomatal conductance, suggesting reduced access to soil moisture. Here we show that lines with the normal 1RS arm have longer roots than lines with the 1RS^RW arm in both field and hydroponic experiments. In the 1RS^RW lines, differences in seminal root length were associated with a developmentally regulated arrest of the root apical meristem (RAM). Approximately 10 d after germination, the seminal roots of the 1RS^RW plants showed a gradual reduction in elongation rate, and stopped growing a week later. Seventeen days after germination, the roots of the 1RS^RW plants showed altered gradients of reactive oxygen species and emergence of lateral roots close to the RAM, suggesting changes in the root meristem. The 1RS^RW lines also showed reduced biomass (estimated by the normalized difference vegetation index) and grain yield relative to the 1RS lines, with larger differences under reduced or excessive irrigation than under normal irrigation. These results suggest that this genetic variation could be useful to modulate root architecture.

Efficient use of the resources required by plants to sustain crop production is considered an important objective in agriculture. In this context, the idea of developing crops with an enhanced ability to utilize mineral nutrients already taken up by roots has been proposed. In recent years powerful tools that allow the association of phenotypic variation with high-resolution genetic maps of crop plants have also emerged. To take advantage of these tools, accurate methods are needed to estimate the internal efficiency of nutrient utilization (ENU) at the whole-plant level, which requires using suitable conceptual and experimental approaches. Here we highlight some inconsistencies in the definitions of ENU commonly used for ENU ‘phenotyping’ at the vegetative stage and suggest that it would be convenient to adopt a dynamic definition. The idea that ENU should provide information about the relationship between carbon and mineral nutrient economies mainly during the period under which growth is actually affected by low internal nutrient concentration is here advocated as a guide for the selection of adequate operational ENU formulae for the vegetative stage. The desirability of using experimental approaches that allow removal of the influence of nutrient acquisition efficiency on ENU estimations is highlighted. It is proposed that the use of simulation models could help refine the conclusions obtained through these experimental procedures. Some potential limitations in breeding for high ENU are also considered.