Biology subjects

Jaskolowski, A.

Publications and source records attributed to Jaskolowski, A..

3 recordsLinked to original sources

bioRxiv2025

The EXS domain of rice PHOSPHATE1 (OsPHO1;2) reduces the low phosphate response through jasmonate signaling

Phosphorus (P) is a vital macronutrient essential for plant growth, and its deficiency significantly hampers agricultural productivity. The PHOSPHATE 1 (PHO1) protein family, characterized by an N-terminal SPX domain, four transmembrane (4TM) domains, and a C-terminal EXS domain, is pivotal in transporting phosphate (Pi) from roots to shoots. Rice, PHO1;2 plays a crucial role in the Pi export process, and defects in this gene cause severe growth retardation and Pi deficiency symptoms even when external Pi levels are adequate. This study examined the roles of the EXS domain and the combined 4TM+EXS domains of OsPHO1;2 in supporting plant growth responses, independent of Pi transport activity, as well as their influence on hormone signaling and gene regulation. Using CRISPR/Cas9, rice lines expressing specific OsPHO1;2 domains (EXS or 4TM+EXS) were created by targeted deletion of particular domain-coding regions. Phenotypic analysis under Pi-sufficient and deficient conditions, as well as phosphate profiling, revealed that EXS lines exhibited notably better growth than loss-of-function mutants, ospho1;2, during early development, despite having similar shoot Pi levels to the null mutant. These lines showed lower levels of defense hormones (jasmonic acid) than ospho1;2 but were comparable to those in the wild type. Conversely, 4TM+EXS lines exhibited growth patterns similar to ospho1;2 mutants. RNA sequencing indicated that the phosphate starvation response (PSR) and defense pathways were less pronounced in the EXS lines compared to ospho1;2 mutants. However, both EXS and 4TM+EXS lines showed seed development defects and reduced total phosphorus content in seeds, mirroring the ospho1;2 phenotype. Heterozygous plants carrying one functional OsPHO1;2 allele displayed normal growth and seed development, indicating the mutations recessive nature. The findings suggest that the EXS domain of OsPHO1;2 can promote plant growth independently of Pi transport by decreasing PSR and modulating defense hormone pathways. This further suggests a signaling role for PHO1 domains beyond direct Pi translocation. Overall, these results enhance our understanding of Pi homeostasis and may help form strategies for breeding P-efficient crops.

molecular biology↗

bioRxiv2024

Editing cis-elements of OsPHO1;2 improved phosphate transport and yield in rice

Increasing grain yield is the main aim of crop improvement, which is globally impacted by the low availability of soil phosphate (Pi). Overexpressing Pi transporters for increasing Pi uptake often result in Pi toxicity and growth retardation. Despite advancements in genetic engineering, targeting cis-regulatory motifs of Pi transporters remains underexplored for understanding plant mechanisms and improving Pi status. Here, we demonstrated that the excision of the transcription inhibitor motif from the promoter of Pi transporter, OsPHO1;2, enhanced its expression and increased root-to-shoot Pi transport, leading to improved grain yield. Using, in-silico and DNA-protein interaction studies, we show the role of OsWRKY6 transcription factor in the negative regulation of OsPHO1;2 expression by binding to the cis-regulatory element (W-box) present in its promoter. oswrky6 knockout lines displayed a higher OsPHO1;2 expressions, and improved shoot Pi levels. Further, we engineered the OsPHO1;2 promoter for precisely removing the W-box and enhancing OsPHO1;2 expression. The phenotypic and physiological evaluation at the vegetative stage shows that OsPHO1;2 promoter edited (OsPHO1;2:PE) lines have increased shoot length, plant biomass and more root-shoot Pi export under low and normal P conditions. Notably, the 33Pi uptake assay reveals that OsPHO1;2:PE lines exhibited enhanced root Pi uptake, supported by higher root-associated Pi transporters (OsPHTs) expression. An extensive agronomical assessment revealed that OsPHO1;2:PE lines acquire increased seed and panicle numbers, thereby increasing yield without affecting seed quality. Our findings offer valuable insight into the potential of promoter editing to raise plants with better Pi use and improved crop yield.

plant biology↗

bioRxiv2021

Arabidopsis Mediator subunit 17 connects transcription with DNA repair after UV-B exposure

Mediator 17 (MED17) is a subunit of the Mediator complex that regulates transcription initiation in eukaryotic organisms. In yeast and humans, MED17 also participates in DNA repair, physically interacting with proteins of the Nucleotide Excision DNA Repair system. We here analyzed the role of MED17 in Arabidopsis plants exposed to UV-B radiation, which role has not been previously described. Comparison of med17 mutant transcriptome to that of WT plants showed that almost one third of transcripts with altered expression in med17 plants are also changed by UV-B exposure in WT plants. To validate the role of MED17 in UV-B irradiated plants, plant responses to UV-B were analyzed, including flowering time, DNA damage accumulation and programmed cell death in the meristematic cells of the root tips. Our results show that med17 and OE MED17 plants have altered responses to UV-B; and that MED17 participates in various aspects of the DNA damage response (DDR). Increased sensitivity to DDR after UV-B in med17 plants can be due to altered regulation of UV-B responsive transcripts; but additionally MED17 physically interacts with DNA repair proteins, suggesting a direct role of this Mediator subunit during repair. Finally, we here also show that MED17 is necessary to regulate the DDR activated by ATR, and that PDCD5 overexpression reverts the deficiencies in DDR shown in med17 mutants. Together, the data presented demonstrates that MED17 is an important regulator of the DDR after UV-B radiation in Arabidopsis plants. One sentence summaryIn Arabidopsis, MED17 regulates the DNA damage response after UV-B exposure transcriptionally modulating the expression of genes and possibly also physically interacting with DNA repair proteins.

plant biology↗