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Burko, Y.

Publications and source records attributed to Burko, Y..

3 recordsLinked to original sources

Structural and coding variation in PHYTOCHROMES A and C underlies differences in flowering time and shade avoidance in wheat

Plant architecture and developmental timing are influenced by light availability, especially in high-density cropping systems, where canopy shading modifies both light intensity and spectral quality. Despite their ecological and agronomical importance, the genetic basis of these responses in wheat remains poorly understood. Here, using a Recombinant Inbred Lines (RILs) population, we investigated phenological and morphological traits under sunlight and simulated canopy shade. We identify a major QTL on chromosome 5A with light-dependent allelic effects, indicating genotype-by-environment variation in developmental responses. This QTL corresponds to a structural rearrangement, consistent with an inversion in the wild emmer reference genome encompassing PHYTOCHROME C (PHYC-A) and VERNALIZATION-1 (VRN-A1), as well as coding polymorphism in PHYC-A. Analysis of a tetraploid wheat diversity panel further showed that natural variation at PHYC-A and an early stop codon in the BB genome copy of PHYTOCHROME A (PHYA-B) on chromosome 4B are associated with differences in heading time. Functional analysis using TILLING-derived phytochrome mutants confirms distinct and complementary roles for PHYA and PHYC in regulating flowering time, plant height, and leaf elongation under simulated canopy shade. These findings highlight the contribution of phytochrome variation to developmental plasticity under canopy-like light environment, thereby extending model insights to agronomically relevant conditions.

plant biology↗

Coordinating the morphogenesis-differentiation balance by tweaking the cytokinin-gibberellin equilibrium

Morphogenesis and differentiation are important stages in organ development and shape determination. However, how they are balanced and tuned during development is not fully understood. In the compound leaved tomato, an extended morphogenesis phase allows for the initiation of leaflets, resulting in the compound form. Maintaining a prolonged morphogenetic phase in early stages of compound-leaf development is dependent on delayed activity of several factors that promote differentiation, including CIN-TCP transcription factor (TF) LA, the MYB TF CLAU and the plant hormone Gibberellin (GA). Here, we investigated the genetic regulation of the morphogenesis-differentiation balance by studying the relationship between LA, CLAU and GA. Our genetic and molecular examination suggest that LA is expressed more broadly than CLAU and determines the spatio-temporal context of CLAU activity. We demonstrate that both LA and CLAU affect the Cytokinin/Gibberellin (CK/GA) balance. LA reduces the sensitivity of the leaf margin to CK, shown before to be also affected by CLAU. CLAU affects leaf active GA content and sensitivity, shown previously to be also influenced by LA. Therefore, LA and CLAU likely function in parallel pathways to promote leaf differentiation by converging on common downstream processes, including the CK/GA balance.

plant biology↗

Shoot and root thermomorphogenesis are linked by a developmental trade-off

Temperature is one of the most impactful environmental factors to which plants adjust their growth and development. While the regulation of temperature signaling has been extensively investigated for the aerial part of plants, much less is known and understood about how roots sense and modulate their growth in response to fluctuating temperatures. Here we found that shoot and root growth responses to high ambient temperature are coordinated during early seedling development. A shoot signaling module that includes HY5, the phytochromes and the PIFs exerts a central function in coupling these growth responses and control auxin levels in the root. In addition to the HY5/PIF-dependent shoot module, a regulatory axis composed of auxin biosynthesis and auxin perception factors controls root responses to high ambient temperature. Together, our findings show that shoot and root developmental responses to temperature are tightly coupled during thermomorphogenesis and suggest that roots integrate energy signals with local hormonal inputs.

plant biology↗