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Nishide, H.

Publications and source records attributed to Nishide, H..

2 recordsLinked to original sources

Transcriptomic dynamics of petal development in the one-day flower species, Japanese morning glory (Ipomoea nil)

Various aspects of Japanese morning glory (Ipomoea nil) petals, such as color, pattern, shape, flower opening time, and senescence, have been extensively studied. To facilitate such studies, transcriptome data were collected from flower petals at 3-h intervals over 3.5 days; the data was collected from 72 h before and 12 h after flower opening, accounting for 29 timepoints. Data analysis revealed substantial transcriptomic changes before and after flower opening. The expression patterns of cell division marker genes indicated that cell division practically stops at approximately 48 h before flower opening. Furthermore, the increased expression of genes encoding transporters for sugars, amino acids, nucleic acids, and autophagy-related genes was observed after flower opening, indicating the translocation of nutrients from senescing petal cells to other developing tissues. Correlations were found between the temporal expression patterns of the three transcriptional regulators and expression patterns of different sets of structural genes within the anthocyanin biosynthesis pathway, indicating differential reliance on each regulator for the activation of specific structural genes. Furthermore, clock genes were identified. Three copies of the clock gene ELF3 did not exhibit circadian rhythms, potentially allowing I. nil to adapt to high-latitude regions. The temporal transcriptome data and interactive database (https://ipomoeanil.nibb.ac.jp/fpkm/) offer valuable insights into gene expression dynamics, periodicity, and correlations and provide a crucial resource for further research on I. nil and other plant species.

plant biology↗

Molecular phylogeny of fucoxanthin-chlorophyll a/c proteins from Chaetoceros gracilis and Lhcq/Lhcf diversity

Diatoms adapt to various aquatic light environments and play major roles in the global carbon cycle using their unique light-harvesting system, i.e., fucoxanthin chlorophyll a/c binding proteins (FCPs). Structural analyses of photosystem II (PSII)-FCPII and photosystem I (PSI)-FCPI complexes from the diatom Chaetoceros gracilis have revealed the localization and interactions of many FCPs; however, the entire set of FCPs has not been characterized. Here, we identified 46 FCPs in the newly assembled genome and transcriptome of C. gracilis. Phylogenetic analyses suggested that these FCPs could be classified into five subfamilies: Lhcr, Lhcf, Lhcx, Lhcz, and novel Lhcq, in addition to a distinct type of Lhcr, CgLhcr9. The FCPs in Lhcr, including CgLhcr9 and some Lhcqs, had orthologous proteins in other diatoms, particularly those found in the PSI-FCPI structure. By contrast, the Lhcf subfamily, some of which were found in the PSII-FCPII complex, seemed to be diversified in each diatom species, and the number of Lhcqs differed among species, indicating that their diversification may contribute to species-specific adaptations to light. Further phylogenetic analyses of FCPs/light-harvesting complex (LHC) proteins using genome data and assembled transcriptomes of other diatoms and microalgae in public databases suggest that our proposed classification of FCPs was common among various red-lineage algae derived from secondary endosymbiosis of red algae, including Haptophyta. These results provided insights into the loss and gain of FCP/LHC subfamilies during the evolutionary history of the red algal lineage. One sentence summaryPhylogenetic analysis of fucoxanthin-chlorophyll a/c proteins in C. gracilis revealed five major subfamilies and one minor subfamily, providing insights into the diversification of light-harvesting systems in red algae.

plant biology↗