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Biology subjects

Toyama, S.

Publications and source records attributed to Toyama, S..

4 recordsLinked to original sources

Linking sediment porosity to taxon-specific patterns of eDNA preservation in a temperate, semi-enclosed bay

Sedimentary environmental DNA provides unique insights into past community dynamics. However, the influence of physical sediment properties, such as porosity, on taxon-specific eDNA preservation remains poorly understood, particularly in temperate inner-bay environments. Therefore, here, we characterized eukaryotic communities in sediment cores from the surface to 6-m depth in the inner and mouth regions of the Uranouchi Bay, a semi-enclosed embayment in temperate Japan. Both 18S rRNA and mitochondrial cytochrome c oxidase subunit I gene metabarcoding revealed marked spatial variation; specifically, inner-bay sediments were enriched in terrestrial plant DNA and dinoflagellates, whereas mouth sediments contained higher proportions of marine diatoms. Vertical profiles further highlighted differences in DNA persistence, with terrestrial and particle-associated taxa retained deeper in the inner-bay sediments. Land-sea connectivity and basin geography strongly shape sedimentary eDNA composition, reflecting both ecological sourcing and preservation bias. We further systematically analyzed the relationship between sediment porosity, a critical physical property governing pore water mobility and solute diffusion, and taxon-specific sedimentary eDNA preservation. To highlight effects of porosity independent of burial depth, we modeled porosity as a function of depth and correlated the residual porosity with the relative abundances of individual phyla. Notably, the phyla exhibited contrasting preservation patterns: Dinoflagellata, Euglenozoa, and Rotifera showed weak to moderate positive correlations with porosity, whereas Chlorophyta and Ochrophyta displayed weak negative correlations. When depth correlations were examined jointly, multiple distinct pattern groups emerged: some taxa (e.g., Dinoflagellata) exhibited negative depth but positive porosity correlations, whereas others showed opposite or neutral patterns. These divergent responses suggest that DNA preservation in marine sediments involves multiple taxon-specific mechanisms rather than a single universal process, with porosity acting as an independent determinant of burial depth. Our results highlight the importance of integrating physical properties of sediments into sedimentary environmental DNA-based paleoenvironmental reconstructions.

ecology↗

Retinoic acid-responsive hox genes in hoxba and hoxbb clusters direct pharyngeal pouch formation in zebrafish

The segmented pharyngeal apparatus is crucial for organ development specific to vertebrates, and its formation relies on the proper development of pharyngeal pouches. While retinoic acid (RA) is known to influence pouch formation, the downstream genes involved have been unclear. In this study, we demonstrate that zebrafish mutants lacking both the hoxba and hoxbb clusters--teleost-specific duplicates of the ancestral HoxB cluster--exhibit a significant loss of posterior pharyngeal pouches and related skeletal elements. This phenotype resembles that observed in raldh2 and pax1a;pax1b mutants. We identify hoxb1a and hoxb1b as RA-dependent genes expressed in the pharyngeal region that are essential for pouch formation. Morpholino-mediated knockdown of these genes replicated the pouch defects and decreased pax1a expression, indicating a regulatory pathway linking RA, Hox, and pax1. Our findings uncover a previously unrecognized role of Hox genes in early pouch segmentation and suggest that RA-responsive HoxB clusters were co-opted during vertebrate evolution to initiate pharyngeal regionalization.

developmental biology↗

Genetic evidence: zebrafish hoxba and hoxbb clusters are essential for the anterior-posterior positioning of pectoral fins

Vertebrate paired appendages, such as the pectoral fins in fish and the forelimbs in tetrapods, arise at specific regions along the anterior-posterior axis of the body. Hox genes have long been considered prime candidates for determining the anteroposterior positioning of these paired appendages during development. Evidence from various model organisms, including mouse and chick, supports a role for Hox genes in limb positioning. However, despite extensive phenotypic analyses of numerous single and compound Hox knockout mice, clear genetic evidence for substantial defects in limb positioning has been limited, leaving questions unresolved. In a previous study, we generated seven distinct hox cluster-deficient mutants in zebrafish. Here, we provide genetic evidence that zebrafish hoxba;hoxbb cluster-deleted mutants specifically exhibit a complete lack of pectoral fins, accompanied by the absence of tbx5a expression in pectoral fin buds. In these mutants, tbx5a expression in the pectoral fin field of the lateral plate mesoderm fails to be induced at an early stage, suggesting a loss of pectoral fin precursor cells. Furthermore, the competence to respond to retinoic acid is lost in hoxba;hoxbb cluster mutants, indicating that tbx5a expression cannot be induced in the pectoral fin buds. We further identify hoxb4a, hoxb5a, and hoxb5b as pivotal genes underlying this process. Although the frameshift mutations in these hox genes do not recapitulate the absence of pectoral fins, we demonstrate that deletion mutants at these genomic loci show the absence of pectoral fins with low penetrance. Our results suggest that, by establishing the expression domains along the anteroposterior axis, hoxb4a, hoxb5a, and hoxb5b within hoxba and hoxbb clusters cooperatively determine the positioning of zebrafish pectoral fins through the induction of tbx5a expression in the restricted pectoral fin field. Our findings also provide insights into the evolutionary origin of paired appendages in vertebrates.

developmental biology↗

An attenuated vaccinia vaccine encoding the SARS-CoV-2 spike protein elicits broad and durable immune responses, and protects cynomolgus macaques and human ACE2 transgenic mice from SARS-CoV-2 and its variants

As long as the coronavirus disease 2019 (COVID-19) pandemic continues, new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) with altered antigenicity will emerge. The development of vaccines that elicit robust, broad, and durable protection against SARS-CoV-2 variants is urgently needed. We have developed a vaccine (rDIs-S) consisting of the attenuated vaccinia virus DIs strain platform carrying the SARS-CoV-2 S gene. rDIs-S induced neutralizing antibody and T-lymphocyte responses in cynomolgus macaques and human angiotensin converting enzyme 2 (hACE2) transgenic mice, and showed broad protection against SARS-CoV-2 isolates ranging from the early-pandemic strain (WK-521) to the recent Omicron BA. 1 variant (TY38-839). Using a tandem mass tag (TMT) -based quantitative proteomic analysis of lung homogenates from hACE2 transgenic mice, we found that, among mice subjected to challenge infection with WK-521, vaccination with rDIs-S prevented protein expression related to the severe pathogenic effects of SARS-CoV-2 infection (tissue destruction, inflammation, coagulation, fibrosis, and angiogenesis) and restored protein expression related to immune responses (antigen presentation and cellular response to stress). Furthermore, long-term studies in mice showed that rDIs-S maintains S protein-specific antibody titers for at least 6 months after a 1st vaccination. Thus, rDIs-S appears to provide broad and durable protective immunity against SARS-CoV-2, including current and possibly future variants.

microbiology↗