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Biology subjects

Shibata, R.

Publications and source records attributed to Shibata, R..

3 recordsLinked to original sources

AtPUP5 functions as a plasma membrane flavin transporter regulating localized riboflavin distribution in Arabidopsis

Riboflavin (vitamin B{square}; RF) and its derivatives flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) are indispensable cofactors for redox reactions in plants. While higher plants possess a conserved pathway for de novo riboflavin biosynthesis, how flavins are transported and spatially distributed between tissues remains unresolved. In particular, the molecular identity of plasma membrane transporters involved in flavin transport in plants remains largely unknown. Here, we identify Arabidopsis purine permease 5 (AtPUP5) as a plasma membrane-localized protein associated with riboflavin transport and its distribution in plants. Using a riboflavin-auxotrophic yeast mutant, we show that AtPUP5 enhances intracellular accumulation of RF and, to a lesser extent, FMN, whereas FAD accumulation is inefficient under the conditions tested. In planta, AtPUP5 overexpression increases RF accumulation following external application. In contrast, loss-of-function mutants do not display defects in bulk RF uptake at the whole-plant level, indicating that AtPUP5 is not essential for global riboflavin acquisition. Notably, AtPUP5 deficiency results in RF overaccumulation in reproductive organs, including inflorescences, siliques, and seeds, irrespective of external RF supply. This organ-specific phenotype is fully suppressed by genetic complementation and coincides spatially with strong AtPUP5 promoter activity in reproductive tissues. These findings suggest that AtPUP5 contributes to the regulation of localized riboflavin distribution in reproductive tissues. Together, our study provides a molecular framework for plasma membrane-mediated regulation of riboflavin distribution in plants and highlights spatial regulation as an important component of flavin homeostasis.

plant biology↗

Dining in the daylight: Nocturnal rhinoceros beetles extend feeding periods on host trees with reduced sap exudation

While the Japanese rhinoceros beetle Trypoxylus dichotomus typically feeds on the sap of the oak Quercus acutissima and the crape myrtle Lagerstroemia subcostata during the night, it exhibits feeding activity both during the day and night when it utilizes the ash tree Fraxinus griffithii. However, the mechanisms underlying the variations in temporal activity patterns remain unknown. We compared feeding rates (measured as body mass increments) and sap exudation rates among F. griffithii, Q. acutissima, and L. subcostata. We found that beetles feeding on L. subcostata and Q. acutissima exhibited significantly higher feeding rates than those feeding on F. griffithii. No significant differences in feeding rates were observed between L. subcostata and Q. acutissima. The sap exudation rate was significantly higher for Q. acutissima than for F. griffithii. However, there were no significant differences in the sap exudation rates between F. griffithii and L. subcostata or between Q. acutissima and L. subcostata. These findings suggest that lower feeding rates on F. griffithii prolong the feeding duration, resulting in daytime activity. While the low sap exudation in L. subcostata seems inconsistent with high feeding rates on this host, this apparent contradiction could be related to the extended duration of sap exudation.

ecology↗

Novel System to Monitor In Vivo Neural Graft Activity After Spinal Cord Injury

Expectations for neural stem/progenitor cell (NS/PC) transplantation as a treatment for spinal cord injury (SCI) are increasing. However, whether and how grafted cells are incorporated into the host neural circuit and contribute to motor function recovery remain unknown. The aim of this project was to establish a novel non-invasive in vivo imaging system to visualize the activity of neural grafts by which we can simultaneously demonstrate the circuit-level integration between the graft and host, and the contribution of graft neuronal activity to host behaviour. We introduced Akaluc, a newly engineered luciferase, under control of a potent neuronal activity-dependent synthetic promoter, E-SARE, into NS/PCs and engrafted the cells into SCI model mice. Through the use of this system, we reveal that the activity of grafted cells was integrated with host behaviour and driven by host neural circuit inputs. This non-invasive system is expected to help elucidate the therapeutic mechanism of cell transplantation treatment for SCI and determine better therapy techniques that maximize the function of cells in the host circuit.

neuroscience↗