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Tokumoto, S.

Publications and source records attributed to Tokumoto, S..

2 recordsLinked to original sources

Intracellular localization and gene expression analysis provide new insights on LEA proteins diversity in anhydrobiotic midge

Anhydrobiosis, an adaptive ability to withstand complete desiccation, is in insects limited to a single species: the nonbiting midge Polypedilum vanderplanki (the sleeping chironomid). Evolution of anhydrobiosis in a single representative of a large genus is associated with drastic changes in genome structure, including the emergence of new multimember gene families directly involved in desiccation tolerance. Among them, Late Embryogenesis Abundant (LEA) proteins, which protect other proteins from aggregation caused by desiccation, are believed to originate via horizontal gene transfer from a bacterial donor. To obtain new insights on the biological background of the expanded 27-member LEA protein group in P. vanderplanki, we investigated the expression of corresponding genes in a P. vanderplanki-derived cell line, capable of anhydrobiosis, in a normal state and during induction of desiccation tolerance. We found that all LEA proteins genes identified in P. vanderplankis genome except PvLea16 and PvLea17 are also expressed in Pv11 cells. Their expression was elevated in response to anhydrobiosis-inducing trehalose treatment. Expression patterns of PvLea genes were well preserved in Pv11 cells in comparison to P. vanderplankis larvae both in the control group and during the anhydrobiosis cycle. We also investigated localization of LEA proteins in Pv11 cells and Sf9 cells and found a different level of conservation in intracellular localization of the protein expressed in mammalian and insect cells.

molecular biology

Three-dimensional analysis of β-cell proliferation by a novel mouse model

Inducing {beta}-cell proliferation could inhibit diabetes progression. Many factors have been suggested as potential {beta}-cell mitogens, but their impact on {beta}-cell replication has not been confirmed due to the lack of a standardized {beta}-cell proliferation assay. In this study, we developed a novel method that specifically labels replicating {beta} cells and yields more reproducible results than current immunohistochemical assays. We established a mouse line expressing the fluorescent ubiquitination-based cell cycle indicator (Fucci2a) reporter only in {beta} cells through Cre-mediated recombination under the control of the rat insulin promoter (RIP-Cre;Fucci2aR). Three-dimensional imaging of optically cleared pancreas tissue from these mice enabled the quantification of replicating {beta} cells in islets and morphometric analysis of islets following mitogen treatment. Intravital imaging of RIP-Cre;Fucci2aR mice revealed cell cycle progression of {beta} cells. Thus, this novel mouse line is a powerful tool for spatiotemporal analysis of {beta}-cell proliferation in response to mitogen stimulation.

cell biology