Biology subjects

Koide, T.

Publications and source records attributed to Koide, T..

14 recordsLinked to original sources

bioRxiv2026

Composition-controlled artificial collagen shows opposing roles of collagen-binding integrins and discoidin domain receptors in neuronal differentiation of PC12 cells

Collagen, a major component of the extracellular matrix, regulates cellular behaviors, such as adhesion, differentiation, and angiogenesis. These functions are mediated by interactions between specific amino acid motifs within the collagen triple-helical structure and collagen-binding biomolecules. These include cell-surface receptors, such as integrins, discoidin domain receptors (DDRs), and syndecans, a family of transmembrane heparan sulfate proteoglycans (HSPGs). Signals mediated by these receptors are integrated to regulate cell fate. However, native collagen simultaneously presents multiple receptor-binding motifs, making it difficult to isolate receptor-specific functions and to evaluate receptor crosstalk. Here, we introduce a composition-controlled artificial collagen matrix platform that enables independent tuning of multiple receptor-binding motifs within a constant triple-helical scaffold. This material was produced by disulfide crosslinking of chemically synthesized collagen-like triple-helical peptides, each bearing a single defined receptor-binding sequence. By varying the mixing ratios of these peptides before crosslinking, we systematically controlled the composition of receptor-binding motifs within the matrices. We applied this platform to nerve growth factor-dependent neuronal differentiation of PC12 cells, a process supported by collagen. Matrices containing only integrin-binding sequences were sufficient to support this differentiation. Incorporation of an HSPG-binding sequence had little additional effect, whereas incorporation of a DDR-binding sequence suppressed integrin-mediated differentiation and coincided with DDR phosphorylation. These results reveal opposing roles of collagen-binding integrins and DDRs in regulating PC12 cell differentiation. Composition-controlled artificial collagen provides a versatile matrix platform for dissecting functional crosstalk among collagen receptors.

bioengineering↗

bioRxiv2026

Platinum Cross-linked Collagen Matrices with Tunable Stiffness as a Platform to Investigate Cellular Mechanosensing

The mechanical properties of the cellular microenvironment are key regulators of cellular physiology. Although the field of cancer mechanobiology has attracted attention, the availability of matrix systems with independently and precisely tunable mechanical properties remains limited. Our group previously developed a collagen gel with enhanced mechanical strength by cross-linking collagen molecules using a platinum complex. In this study, we investigated the tunability of the mechanical properties of the platinum cross-linked collagen gel (PCG) and demonstrated that mechanical parameters can be controlled by varying the amount of the platinum complex. In addition, we examined how matrix mechanical properties modulate the phenotypes of lung adenocarcinoma A549 cells using the collagen matrix. Although A549 cells exhibited significant morphological alterations on stiffer matrices, these changes were not accompanied by classical epithelial-to-mesenchymal transition (EMT). Instead, they were associated with the upregulation of diverse gene expression related to cancer malignancy. We focused on maternal embryonic leucine zipper kinase (MELK) whose gene expression increased on stiffer matrices. Consistently, A549 cells cultured on stiffer matrices displayed enhanced sensitivity to a MELK-targeting anticancer drug. These findings highlight the potential of the matrices with tunable mechanical parameters not only to provide variety of physiological microenvironment but also to advance anticancer drug screening when combined with gene expression analysis. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=100 SRC="FIGDIR/small/720034v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@419074org.highwire.dtl.DTLVardef@72ef67org.highwire.dtl.DTLVardef@1c36e17org.highwire.dtl.DTLVardef@170dc33_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIPlatinum cross-linked collagen gel enables independent tuning of compressive and shear elasticities. C_LIO_LICellular functions may be regulated by matrix mechanical parameters through distinct mechanisms. C_LIO_LICorrelation analysis between matrix mechanical parameters and cancer cell gene expression provides a rational strategy for therapeutic drug screening. C_LI

bioengineering↗

bioRxiv2026

Molecular basis of collagen triple helix recognition by VWF A-like domain 2 of collagen VII: Implications for interlaced anchoring fibril formation

Anchoring fibrils formed by collagen VII play a critical role in stabilizing the dermal-epidermal junction. The N-terminal non-collagenous (NC1) domain of collagen VII binds firmly to basement membrane components including collagen IV and has also been reported to interact with mesenchymal fibrillar collagens via its von Willebrand factor A-like domain 2 (A2 domain). To elucidate how collagen VII recognizes fibrillar collagen, we performed yeast two-hybrid screening using a triple-helical random peptide library, which resulted in the identification of a Met-Gly-{Phi} ({Phi}; aromatic amino acid residue) motif. Biochemical analysis with synthetic triple-helical peptides revealed a binding preference of Trp > Phe as the {Phi} residue by the A2 domain despite Trp being absent in native collagens. The crystal structure of the A2 domain in complex with the Nle (Met surrogate)-Gly-Trp-containing peptide revealed a unique mechanism by which two distinct hydrophobic pockets of the A2 domain accommodate the Nle and Trp residues corresponding to the Met-Gly-{Phi} motif, engaging all three chains of the triple helix. Subsequent molecular dynamics simulations demonstrated that the A2 domain recognizes the corresponding native Met-Gly-Phe motif in a similar manner, but with lower affinity, implying a transient interaction with mesenchymal collagens. The findings obtained in this work suggest models in which transient A2-triple helix interaction promotes the recruitment of collagen I and III fibrils into the arc-shaped structure of anchoring fibrils. This also provides a foundation for linking structural understanding to skin fragility diseases caused by collagen VII dysfunction.

biochemistry↗

bioRxiv2025

Chromosome-scale genomes of two wild flowering cherrys (Cerasus itosakura and C. jamasakura) provide insights into structural evolution in Prunus

Flowering cherries (genus Cerasus) are iconic trees in Japan, celebrated for their cultural and ecological significance. Despite their prominence, high-quality genomic resources for wild Cerasus species have been limited. Here, we report chromosome-level genome assemblies of two representative Japanese cherries: Cerasus itosakura, a progenitor of the widely cultivated C. xyedoensis Somei-yoshino, and Cerasus jamasakura, a traditional popular wild species endemic to Japan. Using deep PacBio long-read and Illumina short-read sequencing, combined with reference-guided scaffolding based on near-complete C. speciosa genome, we generated assemblies of 259.1 Mbp (C. itosakura) and 312.6 Mbp (C. jamasakura), with both >98% BUSCO completeness. Consistent with their natural histories, C. itosakura showed low heterozygosity, while C. jamasakura displayed high genomic diversity. Comparative genomic analyses revealed structural variations, including large chromosomal inversions. Notably, the availability of both the previously published C. speciosa genome and our new C. itosakura genome enabled the reconstruction of proxy haplotypes for both parental lineages of Somei-yoshino. Comparison with the phased genome of Somei-yoshino revealed genomic discrepancies, suggesting that the cultivar may have arisen from genetically distinct or admixed individuals, and may also reflect intraspecific diversity. Our results offer genomic foundations for evolutionary and breeding studies in Cerasus and Prunus.

genomics↗

bioRxiv2025

Triple-helical ligands selectively targeting the closed αI domain of integrin α2β1

Integrins 1{beta}1, 2{beta}1, 10{beta}1, and 11{beta}1 are known to recognize the GxxGEx motif of the collagen triple helix through their I domains, with the Glu residue engaging the domain via a divalent metal cation. The binding amino acid sequences containing these motifs, identified from native collagen, exhibit low subtype selectivity. Here we identify novel triple-helical peptides that selectively bind the 2I domain independently of Glu and metal ions. Yeast two-hybrid screening of randomized triple-helical peptide libraries yielded non-natural sequences in which the canonical Glu was replaced by aliphatic residues such as Met. X-ray crystal structural analysis of the representative variant GFOGMR in complex with the 2I domain revealed a new binding mode. In this mode, peptides are recognized by the closed, inactive conformation of the 2I domain without metal coordination. This cryptic interaction, likely unused by native ligands, provides a new basis for the design of subtype-specific ligands targeting collagen-binding integrins.

biochemistry↗

bioRxiv2025

A facile method for fluorescent visualization of newly synthesized fibrous collagen by capturing the allysine aldehyde groups serving as cross-link precursors

The fibrous structures of collagen provide physical strength and stability to tissues and organs. Abnormalities in their orientation, growth, and remodeling cause morphogenetic defects and diseases including fibrosis, highlighting the importance of understanding how collagen fibers are organized within tissues. However, this process remains difficult to study, as methods for fluorescently labeling collagen fibers with simple protocols and visualizing their three-dimensional structure are still limited. Here we describe a convenient method for fluorescent labeling of collagen fibers in vertebrate tissues. Using DAF-FM, a probe originally developed for nitric oxide detection, premature collagen fibers can be visualized through covalent binding to allysine residues, which serve as precursors of collagen cross-linking. We further show that combining two probes with different emission spectra, DAF-FM and DAR-4M, enables pulse-chase labeling of newly synthesized collagen fibers. This approach provides a practical tool for investigating collagen dynamics during tissue development and remodeling.

developmental biology↗

bioRxiv2025

Avid lysosomal acidification in fibroblasts of the Mediterranean mouse Mus spretus

Failures of the lysosome-autophagy system are a hallmark of aging and many disease states. As a consequence, interventions that enhance lysosome function are of keen interest in the context of drug development. Throughout the biomedical literature, evolutionary biologists have found cases in which challenges faced by humans in clinical settings have been resolved by non-model organisms adapting to wild environments. Here, we used a primary cell culture approach to survey lysosomal characteristics in species of the genus Mus. We found that fibroblasts from M. spretus, a wild Mediterranean mouse, exhibited elevated lysosomal mass and enzyme activity along with reduced activity of {beta}-galactosidase, a classical marker of cellular senescence, compared to those from M. musculus, a related species adapted to human-associated environments. We propose that classic laboratory models of lysosome function and senescence may reflect characters that diverge from the phenotypes of wild mice. The M. spretus phenotype may ultimately serve as a blueprint for interventions that ameliorate lysosomal dysfunction under conditions of stress and disease.

evolutionary biology↗

bioRxiv2024

Tameness selection pressure affects gut virome diversity in mice

The gut microbiome, a complex ecosystem comprising bacteria, viruses, archaea, fungi, and other microorganisms, plays a pivotal role in host health, immunity, and behaviour. Among its components, bacteriophages and viruses that infect bacteria significantly influence microbial community dynamics by affecting bacterial diversity, function, and evolution. Despite extensive research on bacterial components, the viral metagenome (virome) remains relatively unexplored. This study investigated the effect of selective breeding for tameness on the gut virome of wild heterogeneous stock (WHS) mice. WHS mice were selectively bred for active tameness, resulting in four groups: S1 and S2 (selected for tameness), and C1 and C2 (non-selected). In previous study, we observed an increased abundance of Limosilactobacillus reuteri in tame groups compared to non-selected groups, as well as a tameness-promoting effect of L. reuteri with long-term administration. Given the regulatory role of phages in bacterial populations, this study focused on analysing the gut virome using shotgun metagenome sequencing data. From the 84 samples, we generated 6078 non-redundant viral operational taxonomic units (vOTUs) and identified the hosts of 3,065 of these vOTUs. Significant differences in gut virome beta diversity were observed between the selectively bred and control groups, suggesting that tameness selection exerts distinct pressure on the virome. Additionally, phage-host interaction analysis revealed strong correlations between specific phages and their bacterial hosts, indicating a co-occurrence that influences host behaviour. Overall, this study provides novel insights into the role of the gut virome in shaping host behaviour and highlights the broader implications of microbial contributions to domestication and selective breeding outcomes.

microbiology↗

bioRxiv2024

Decoding the Centromeric Region with a Near Complete Genome Assembly of the Oshima Cherry Cerasus speciosa

The Oshima cherry (Cerasus speciosa), which is endemic to Japan, has significant cultural and horticultural value. In this study, we present a near complete telomere-to-telomere genome assembly for C. speciosa, derived from the old growth "Sakurakkabu" tree on Izu Oshima Island. Using Illumina short-read, PacBio long-read, and Hi-C sequencing, we constructed a 269.3 Mbp genome assembly with a contig N50 of 32.0 Mbp. We examined the distribution of repetitive sequences in the assembled genome and identified regions that appeared to be centromeric. Detailed structural analysis of these putative centromeric regions revealed that the centromeric regions of C. speciosa comprised repetitive sequences with monomer lengths of 166 or 167 bp. Comparative genomic analysis with Prunus sensu lato genome revealed structural variations and conserved syntenic regions. This high-quality reference genome provides a crucial tool for studying the genetic diversity and evolutionary history of Cerasus species, facilitating advancements in horticultural research and the preservation of this iconic species.

genomics↗

bioRxiv2024

Comparative Analysis of Tickling and Conspecific Play in Tame Mice and Golden Hamsters

Social play behavior is a fundamental aspect of animal interaction, shaping social bonds and enhancing cognitive capacity. While studies on human-animal play interactions have primarily focused on a few selected species, research on rodents beyond rats remains scarce. We, therefore, addressed the dynamics of social play in tame mice, selectively bred to approach human hands, and golden hamsters, comparing their responses during interactions with humans and conspecifics. Tame mice exhibited heightened playfulness with humans, marked by increased vocalizations and chasing behavior, in addition to increased interactions with tame conspecifics compared to unselected control mice. Hamsters demonstrated a stronger inclination towards conspecific interactions. Notably, vocalization patterns varied between heterospecific and conspecific engagement in both species, suggesting context-dependent communication. These findings offer insights into the evolutionary basis influencing social play across species with differing social structures. Understanding these mechanisms enriches our comprehension of the diverse pathways through which animals form social bonds.

animal behavior and cognition↗

bioRxiv2024

Enhanced tameness by Limosilactobacillus reuteri from gut microbiota of selectively bred mice

Domestication alters animal behaviour, primarily their tameness. In this study, we examine the effect of gut bacteria on mouse tameness. We previously conducted selective breeding for active tameness, defined as the motivation to approach a human hand, using genetically heterogeneous mice derived from eight wild inbred strains. We examined gut microbiota in the selectively bred mice by analysing faecal samples from 80 mice through shotgun metagenomic analysis. In the current study, we found that the selectively bred mice exhibit higher levels of active tameness as well as higher levels of blood oxytocin, which plays a key role in social behaviours. Selection for tameness did not substantially alter the taxonomic or functional diversity of the gut microbiota. However, we observed an increased abundance of Limosilactobacillus reuteri in the selected groups and higher pyruvate levels in their plasma. We isolated L. reuteri strains secreting extracellular pyruvate from mice faeces and administrated the cultured bacteria through drinking water. Mice treated with L. reuteri showed higher colonization of the bacteria in the gut, as well as higher levels of active tameness behaviour and blood oxytocin. Additionally, we generated 374 high-quality metagenome-assembled genomes (MAGs) of bacteria across 11 phyla. This collection includes 27 novel species level bacterial MAGs not previously known to exist in the mouse gut. This study elucidates the potential role of L. reuteri in the animal domestication process and explores the underlying mechanisms that may influence this process.

microbiology↗

bioRxiv2023

A complex regulatory cascade involving quorum sensing regulates siderophore-mediated iron homeostasis in Chromobacterium violaceum

Iron is a transition metal used as a cofactor in many biochemical reactions. In bacteria, iron homeostasis involves Fur-mediated de-repression of iron uptake systems, such as the iron-chelating compounds siderophores. In this work, we identified and characterized novel regulatory systems that control siderophores in the environmental opportunistic pathogen Chromobacterium violaceum. Screening of a 10,000-transposon mutant library for siderophore halos on PSA-CAS plates identified seven possible regulatory systems involved in siderophore-mediated iron homeostasis in C. violaceum. Further characterization revealed a regulatory cascade that controls siderophores involving the transcription factor VitR acting upstream of the quorum sensing (QS) system CviIR. Mutation of the regulator VitR led to an increase in siderophore halos, and a decrease in biofilm, violacein, and protease production. We determined that these effects occurred due to VitR-dependent de-repression of vioS. Increased VioS leads to direct inhibition of the CviR regulator by protein-protein interaction. Indeed, insertion mutations in cviR and null mutation of cviI and cviR led to an increase of siderophore halos. RNA-seq of the cviI and cviR mutants revealed that CviR regulates CviI-dependent and CviI-independent regulons. Classical QS-dependent processes (violacein, proteases, and antibiotics) were activated at high cell density by both CviI and CviR. However, genes related to iron homeostasis and many other processes were regulated by CviR but not CviI, suggesting that CviR acts without its canonical CviI autoinducer. Our data revealed a complex regulatory cascade involving QS that controls siderophore-mediated iron homeostasis in C. violaceum. ImportanceThe iron-chelating compounds siderophores play a major role in bacterial iron acquisition. Here, we employed a genetic screen to identify novel siderophore regulatory systems in Chromobacterium violaceum, an opportunistic human pathogen. Many mutants with increased siderophore halos had transposon insertions in genes encoding transcription factors, including a novel regulator called VitR, and CviR, the regulator of the quorum sensing (QS) system CviIR. We found that VitR is upstream in the pathway and acts as a dedicated repressor of vioS, which encodes a direct CviR-inhibitory protein. Indeed, all QS-related phenotypes of a vitR mutant were rescued in a vitRvioS mutant. At high cell density, CviIR activated classical QS-dependent processes (violacein, proteases, and antibiotics production). However, genes related to iron homeostasis and type-III and type-VI secretion systems were regulated by CviR in a CviI- or cell density-independent manner. Our data unveil a complex regulatory cascade integrating QS and siderophores in C. violaceum.

microbiology↗

bioRxiv2023

A yeast two-hybrid system to obtain triple-helical ligands from combinatorial random peptide libraries

Many bioactive proteins interact with collagen, recognizing amino acid sequences displayed on the triple helix. We report here a selection strategy to obtain triple-helical peptides that interact with the proteins from a combinatorial random library constructed in yeast cells. This system enables us to select them using the standard two-hybrid protocol, detecting interactions between triple-helical peptides and target proteins fused to the GAL4-activating and binding domains, respectively. The library was constructed having triple-helical peptides with a "host-guest" design in which host helix-stabilizing regions flanked guest random sequences. Using this system, we selected peptides that bind to pigment epithelium-derived factor (PEDF), a collagen-binding protein that shows anti-angiogenic and neurotrophic activities, from the libraries. Two-step selections from the total random library and subsequently from the second focused library yielded new PEDF-binding sequences that exhibited a comparable affinity to or more potent than that of the native PEDF-binding sequence in collagen. The obtained sequences also contained a variant of the PEDF-binding motif that did not match the known motif identified from the native collagen sequences. This combinatorial library system allows the chemical space of triple-helical peptides to be screened more widely than that found in native collagen, thus increasing the expectation of obtaining more specific and high-affinity peptides.

biochemistry↗

bioRxiv2022

A genome-scale atlas reveals complex interplay of transcription and translation in an archaeon

The scale of post-transcriptional regulation and the implications of its interplay with other forms of regulation on environmental acclimation is underexplored for organisms of the domain Archaea. Here, we have investigated the scale of post-transcriptional regulation in the extremely halophilic archaeon Halobacterium salinarum NRC-1 by integrating transcriptome-wide locations of transcript processing sites (TPS) and SmAP1 binding, genome-wide locations of antisense RNAs (asRNAs), and consequences of RNase_2099C knockout on differential expression of all genes. This integrated analysis has discovered that 54% of all protein-coding genes in the genome of this haloarchaeon are likely targeted by multiple mechanisms for putative post-transcriptional processing and regulation, with about 20% of genes likely regulated by combinatorial schemes involving SmAP1, asRNAs, and RNase_2099C. Comparative analysis of mRNA levels (RNA-Seq) and protein levels (SWATH-MS) for 2,579 genes over four phases of batch culture growth in complex medium has generated additional evidence for conditional post-transcriptional regulation of 7% of all protein-coding genes. We demonstrate that post-transcriptional regulation may act to fine-tune specialized and rapid acclimation to stressful environments, e.g., as a switch to turn on gas vesicle biogenesis to promote vertical relocation in anoxic conditions and to modulate frequency of transposition by IS elements of the IS200/IS605, IS4, and ISH3 families. Findings from this study are provided as an atlas in a public web resource (https://halodata.systemsbiology.net). IMPORTANCEWhile the transcriptional regulation landscape of archaea has been extensively investigated, we currently have limited knowledge about post-transcriptional regulation and its driving mechanisms in this domain of life. In this study, we collected and integrated omics data from multiple sources and technologies to infer post-transcriptionally regulated genes and the putative mechanisms modulating their expression at the protein level in Halobacterium salinarum NRC-1. The results suggest that post-transcriptional regulation may drive environmental acclimation by regulating hallmark biological processes. To foster discoveries by other research groups interested in the topic, we extended our integrated data to the public in the form of an interactive atlas (https://halodata.systemsbiology.net).

systems biology↗