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Noda, A.

Publications and source records attributed to Noda, A..

3 recordsLinked to original sources

Predator-Induced Tail Coloration Toward Diverse Dragonfly Nymphs in Tadpoles of the Japanese Tree Frog (Dryophytes japonicus)

Anuran larvae can change their coloration and morphology to avoid predation. Particularly, some tadpoles in the genus Dryophytes in the Americas develop deep tail fins and bright orange tail coloration in response to predators such as dragonfly nymphs. These conspicuous tails are hypothesized to attract predator attacks, protecting vital body parts from fatal injuries. However, it remains unclear whether the extent of the induced phenotypic changes differs between various predators with distinct feeding patterns and habitats. To explore this, we reared tadpoles of the East Japan tree frog, Dryophytes leopardus, with four dragonfly species, water bug, water scorpion, or newt, and measured phenotypic changes, especially focusing on tail coloration. We found that the aeshnid Anax nigrofasciatus, a sit- and-wait predator that climbs on aquatic vegetation, induced bright orange and broad tails of tadpoles. Other odonate species that forage in and on the substrate also elicited tail coloration or deeper larval tails, but it took more time to induce the tadpoles response compared to A. nigrofasciatus. In contrast, non-odonate predators did not induce color and morphological changes. This study provides the first evidence of predator-induced tail coloration in an Asian species of Dryophytes, which appears to be a defensive response specifically to dragonfly nymphs, as visually adept predators. Moreover, the differences in the extent and timing of the phenotypic changes among odonate species suggest that anti-predator phenotypes are modulated based on relative predation risks, considering the predators foraging patterns and visual capabilities, thereby allowing tadpoles to minimize physiological costs and unintended risks associated with the induced traits.

ecology↗

Intraplacental injection of human iPSC-derived PDX1+ pancreatic progenitors prolongs Pdx1-deficient mice survival

Interspecies chimeras comprising human tissues have potential for use in disease modeling and regenerative medicine. Here, we successfully transplanted human induced pluripotent stem cell (iPSC)-derived PDX1+ pancreatic progenitor cells into Pdx1-deficient mouse embryos via intraplacental injection. The engrafted human cells predominantly localized to the duodenum, produced insulin, and extended the lifespan of Pdx1-/- mice by up to 10 days after birth. Transcriptomic analyses confirmed human pancreatic gene expression in human cells engrafted into the mouse duodenum. Our findings demonstrated the feasibility of generating interspecies chimeras with functional human pancreatic cells through in utero transplantation of lineage-committed progenitors. This approach circumvents developmental barriers while minimizing ethical concerns associated with PSCs. However, the incomplete rescue of the Pdx1-/- phenotype highlights the need for further research to enhance human cell engraftment and tissue integration. Overall, this study provides a foundation for developing human-animal chimera models for studying human development and regenerative therapies.

cell biology↗

Deep embedded clustering by relevant scales and genome-wide association study in autism

The etiology of autism spectrum disorders (ASD) remains unclear. Stratifying patients with ASD may help to identify genetically homogeneous subgroups. Using a deep embedded clustering algorithm, we conducted cluster analyses of Simons Foundation Powering Autism Research for Knowledge (SPARK) datasets and performed genome-wide association studies (GWAS) of the clusters. We observed no significant associations in the conventional GWAS comparing all patients to all controls. However, in the GWAS, comparing patients divided into clusters with similar phenotypes to controls (cluster-based GWAS), we identified 90 chromosomal loci that satisfied the P < 5.0 x 10-8, several of which were located within or near previously reported candidate genes for ASD. Our findings suggest that clustering may successfully identify subgroups with relatively homogeneous disease etiologies.

genomics↗