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Isoda, M.

Publications and source records attributed to Isoda, M..

4 recordsLinked to original sources

From photoprotection to growth: shifts in high-light acclimation strategies associated with molecular evolutionary rates in duckweeds

Molecular evolutionary rates vary widely among lineages, yet the biological processes generating this variation remain poorly understood. In plants, which lack an early-segregated germline, growth- and environment-dependent physiology could itself influence mutation accumulation and, ultimately, substitution rates. Here we examine this possibility in duckweeds (Araceae, Lemnoideae), whose closely related lineages differ severalfold in sequence divergence. Nonsynonymous and synonymous divergence scaled proportionally across all six lineages examined, indicating that this heterogeneity does not reflect differences in selective constraint and instead points to variation in mutation rate. Lineages without prominent anthocyanin accumulation occupied lower latitudes and, under high light, sustained higher relative growth rates and higher photosynthetic efficiency. Comparing the early-diverging, anthocyanin-accumulating Spirodela polyrhiza with the late-diverging, anthocyanin-free Wolffia australiana revealed contrasting acclimation strategies: S. polyrhiza preferentially induced photoprotective pathways, including anthocyanin biosynthesis and non-photochemical quenching, whereas W. australiana instead expanded mitochondrial oxidative phosphorylation together with the cytosolic translational machinery, and broadly remodeled primary metabolism. Duckweed lineages therefore differ in how they balance photoprotection against photochemical energy use and downstream metabolic capacity, a divergence that may be associated with their lineage-specific molecular evolutionary rates.

evolutionary biology↗

No circadian clock-gene circuit in the generation of cellular bioluminescence rhythm of CaMV35S::PtRLUC in duckweed

Physiological circadian rhythms are coordinated in the plant body in an orderly manner. The coordination of time information has been studied from the aspects of cell-cell local coupling and long-distance communication between tissues. These studies were based on the idea that the behavior of the clock gene circuit represents the physiological rhythms. Here we report the cellular circadian rhythm of a bioluminescence reporter which is not governed by the clock gene circuit in the expressing cells. Using a dual-color bioluminescence monitoring system in Lemna minor transfected with the AtCCA1::LUC+ and CaMV35S::PtRLUC reporters, cellular bioluminescence rhythms with different free-running periods (FRPs) were detected in the same cells. Co-transfection experiments with the two reporters and a clock gene overexpressing effector revealed that the circadian properties of the AtCCA1::LUC+ rhythm, but not those of the CaMV35S::PtRLUC rhythm, were altered in the cells with a dysfunctional clock gene circuit. This indicates that the AtCCA1::LUC+ rhythm is a direct output of the cellular circadian clock while the CaMV35S::PtRLUC rhythm is not. After plasmolysis, the CaMV35S::PtRLUC rhythm disappeared while the AtCCA1::LUC+ rhythm persisted. The plant circadian system consists of both cell-autonomous rhythms and non-cell-autonomous rhythms that are unaffected by the cellular clock.

plant biology↗

Interspecific divergence of circadian properties in duckweed plants

O_LIThe circadian clock system is widely conserved in plants; however, divergence in circadian rhythm properties is poorly understood. We conducted a comparative analysis of the circadian properties of closely related duckweed species. C_LIO_LIUsing a particle bombardment method, a circadian bioluminescent reporter was introduced into duckweed plants. We measured bioluminescence circadian rhythms of eight species of the genus Lemna and seven species of the genus Wolffiella at various temperatures (20, 25, and 30 {degrees}C) and light conditions (constant light or constant dark). Wolffiella species inhabit relatively warm areas and lack some tissues/organs found in Lemna species. C_LIO_LILemna species tended to show robust bioluminescence circadian rhythms under all conditions, while Wolffiella species showed lower rhythm stability, especially at higher temperatures. For Lemna, two species (L. valdiviana and L. minuta) forming a clade showed relatively lower circadian stability. For Wolffiella, two species (W. hyalina and W. repanda) forming a clade showed extremely long period lengths. C_LIO_LIThe circadian properties of species primarily reflect their phylogenetic positions. The relationships between geographical and morphological factors and circadian properties are also suggested. C_LI

plant biology↗

Detection of uncoupled circadian rhythms in individual cells of Lemna minor by using a dual-color bioluminescence monitoring system

The plant circadian oscillation system is based on the circadian clock of individual cells and coordinates the circadian behavior of the plant body. To observe the cellular circadian behavior of both the oscillator and its output in plants, we developed the dual-color bioluminescence monitoring system that automatically measured the luminescence of two luciferase reporters simultaneously at a single-cell level. We selected a yellow-green-emitting firefly luciferase (LUC+) and a red-emitting luciferase (PtRLUC) that is a mutant form of Brazilian click beetle ELUC. We used AtCCA1::LUC+ and CaMV35S::PtRLUC to observe the cellular behavior of the oscillator and output, respectively. These bioluminescent reporters were introduced into the cells of a duckweed, Lemna minor, by particle bombardment. Time series of the bioluminescence of individual cells in a frond were obtained using a dual-color bioluminescence monitoring system with a green-pass- and red-pass filter. Luminescence intensities from the LUC+ and PtRLUC of each cell were calculated from the filtered luminescence intensities. We succeeded in reconstructing the bioluminescence behaviors of AtCCA1::LUC+ and CaMV35S::PtRLUC in the same cells. Under prolonged constant light conditions, AtCCA1::LUC+ showed a robust circadian rhythm in individual cells in an asynchronous state in the frond, as previously reported in studies using other plants. In contrast, CaMV35S::PtRLUC stochastically showed circadian rhythms in a synchronous state. Thus, we clearly demonstrated the uncoupling between the oscillator and output in individual cells. This dual-color bioluminescence monitoring system is a powerful tool to analyze various stochastic phenomena accompanying large cell-to-cell variation in gene expression. Significance statementWe succeeded in establishing the worlds first dual-color bioluminescence monitoring system at a single-cell level that enables simultaneous measurement of the luminescence activities of two reporter genes in plants. This system is a strong tool to analyze stochastic phenomena, and we clearly demonstrated the uncoupling of rhythmic behavior between two bioluminescent reporters in individual cells that stochastically occurred in the same plant.

plant biology↗