Biology subjects

Hata, Y.

Publications and source records attributed to Hata, Y..

12 recordsLinked to original sources

bioRxiv2026

Generation of KARRIKIN INSENSITIVE2 loss-of-function mutants in Ceratopteris richardii using a CRISPR/Cas9 system based on ribozyme-gRNA-ribozyme (RGR) technology

Plant hormones regulate almost every aspect of plant growth and development. KARRIKIN INSENSITIVE 2 (KAI2)-dependent signaling, which is thought to transduce signals derived from an unidentified ligand known as the KAI2 ligand (KL), regulates numerous traits, including seed germination in angiosperms and vegetative reproduction in bryophytes. The origin of KAI2 is believed to be ancient, and the evolution of its signaling pathways remains of significant interest. Ferns represent critical lineages for elucidating the evolution of land plant traits and growth mechanisms that enabled adaptation to terrestrial environments. Therefore, functional studies of key components of this pathway in ferns are essential for understanding the evolutionary trajectory of KAI2-dependent signaling during vascular plant diversification. However, experimental platforms for the CRISPR/Cas9 system, a powerful tool for investigating gene function, remain undeveloped in ferns. Here, we report an efficient CRISPR/Cas9 system based on ribozyme-gRNA-ribozyme (RGR) technology in the model fern, Ceratopteris richardii (C. richardii). We generated loss-of-function mutants of the KAI2 ortholog in C. richardii (CrKAI2), as well as the signaling components CrMAX2 and CrSMXL. We demonstrate that exogenous application of an artificial KL agonist increases the expression of KAI2-dependent signaling responsive genes in wild type plants; this response is abolished in Crkai2 mutants. These findings indicate that KAI2-dependent signaling is conserved in C. richardii. Furthermore, this study proposes an efficient CRISPR/Cas9 method that will facilitate genetic studies in ferns.

plant biology↗

bioRxiv2025

Group-level matching behavior in phototaxis of acoel flatworm, Praesagittifera naikaiensis.

The matching law, which posits that animals allocate their responses in proportion to the rate of reinforcement, has been supported across diverse animal taxa. Although originally formulated in the context of operant choice, matching also applies to time allocation in foraging and to Pavlovian responses, indicating its generality across behavioral domains. However, empirical evidence has thus far been largely limited to vertebrates and arthropods. Addressing the broader applicability of this principle requires extending investigations beyond these taxonomic groups, across a wider phylogenetic spectrum. Here, we examined phototactic behavior in the acoel flatworm Praesagittifera naikaiensis, a species that acquires nutrients through photosynthesis by symbiotic algae and exhibits positive phototaxis. Using a custom-built T-maze in which the number of illuminated LEDs varied across arms, we found that the animals distributed themselves in proportion to relative brightness, consistent with matching behavior. Moreover, prior exposure to light for 24 hours attenuated this pattern. This manipulation was intended to induce a state of nutritional sufficiency, and the resulting decline in phototactic responses suggests that internal physiological states can modulate even seemingly reflexive locomotor behaviors.

animal behavior and cognition↗

bioRxiv2025

MAX2-dependent signaling regulates the transition from 2D to 3D growth by suppressing cytokinin accumulation in Physcomitrium patens

Plants undergo distinct developmental phases throughout their life cycle. Proper regulation of the timing of phase transition in response to internal and external cues is crucial to optimize proliferation and reproduction. In Physcomitrium patens (P. patens), a moss, the transition from growth of filamentous tissue growth called protonema to gametophore bud formation represents a shift from two-dimensional (2D) to three-demensional (3D) growrh, ultimately leading to reproductive development. MORE AXILLARY GROWTH2 (MAX2), an F-box protein, targets repressor proteins in the KARRIKIN INSENSITIVE2 (KAI2)-dependent signaling pathway for degradation via the 26S proteasome-dependent pathway. KAI2 perceives an unidentified ligand known as KAI2 ligand (KL) as well as karrikins. The four SMAX1-LIKE (SMXL) family proteins work as suppressors in the MAX2-dependent signaling in P. patens. Gametophore bud formation was accelerated when MAX2-dependent signaling was disrupted, while it was delayed in Ppsmxls, loss of function mutants of the PpSMXLs. These results indicate that MAX2-dependent signaling suppresses gametophore bud formation in P. patens, which has not been previously described. We demonstrate that cytokinin activity and contents are increased in Ppmax2 mutants, and cytokinin application rescued the delay in bud formation in Ppsmxl mutants, suggesting that MAX2-dependent signaling suppresses cytokinin accumulation. The four SMXL genes redundantly act to promote gametophore bud formation; PpSMXLC and PpSMXLD, which contain the conserved degron sequence, act as the repressor of MAX2-dependent signaling, while PpSMXLA and PpSMXLB function independent of proteolysis-dependent signaling. Based on these findings, we propose that modulating cytokinin activity to control developmental phase transition may be a conserved role of MAX2-dependent signaling in bryophytes. Significance StatementPlant hormones, both individually and in combination, regulate almost all aspects of plant growth and development. Gametophore bud formation in Physcomitrium patens, a moss, marks the transition from two-dimensional (2D) filamentous growth to three-dimensional (3D) shoot growth. We demonstrate that gametophore bud formation is controlled by the sequential action of two plant hormones, KL, an unidentified hormone that is transduced through MAX2-dependent signaling, and cytokinin. Four SMXL genes, repressors in MAX2-dependent signaling, redundantly promote bud formation: two function within the signaling pathway, while the other two operate independently of it. Our findings uncover novel mechanisms that directly link MAX2-dependent signaling to developmental phase transition by regulating stem cell activity, achieved through the regulation of cytokinin accumulation in Physcomitrium patens.

plant biology↗

bioRxiv2024

KAI2-dependent signaling controls vegetative reproduction in Marchantia polymorpha through activation of LOG-mediated cytokinin synthesis

Marchantia polymorpha reproduces vegetatively (asexually) by producing propagules known as gemmae within gemma cups and sexually through spores. We previously reported that KARRIKIN INSENSITIVE 2 (KAI2)-dependent signaling promotes gemma cup and gemma formation. KAI2A perceives unidentified endogenous ligand(s), tentatively referred to as KAI2 ligands (KL). Perception of KL by KAI2 triggers MAX2-dependent proteolysis of MpSMXL. In this study, we identified genes working downstream of KAI2-dependent signaling in M. polymorpha. We found that KAI2-dependent signaling positively controls the expression of MpLONLEY GUY (MpLOG), encoding a cytokinin biosynthesis enzyme. Disruption of the MpLOG function decreased endogenous cytokinin levels and caused defects similar to KAI2-dependent signaling mutants. Moreover, supplying exogenous cytokinins rescued the defects of Mplog and KAI2-dependent signaling mutants, implying that cytokinins work downstream of KAI2-dependent signaling. Activation of MpLOG by KAI2-dependent signaling occurs in a highly cell-type-specific manner, leading to cell-specific induction of GEMMA CUP-ASSOCIATED MYB1 (GCAM1), the master regulator of vegetative reproduction of M. polymorpha. We propose a genetic cascade, starting from KAI2-dependent signaling, that promotes vegetative reproduction through the induction of MpLOG and GCAM1. The interaction between KAI2-dependent signaling and cytokinin in M. polymorpha provides a novel insight into the function and evolution of KAI2-dependent signaling.

plant biology↗

bioRxiv2024

snRNA-seq analysis of the moss Physcomitrium patens reveals a conserved cytokinin-ESR module promoting pluripotent stem cell identity

The shoot apical meristem (SAM), which contains pluripotent stem cells, serves as the source of the entire shoot system in land plants. To uncover the mechanisms underlying SAM development and its orign, we employed single-nucleus RNA sequencing technology in Physcomitrium patens, which contains a single stem cell known as the gametophore apical cell. We identified distinct cell clusters representing major cell types of the P. patens gametophyte, including the gametophore apical cells. We revealed dynamic gene expression changes during cell fate progression in the gametophore apical cell and found upregulation of cytokinin biosynthesis genes in this cell. We also identified ENHANCER OF SHOOT REGENERATION 1 (ESR1) orthologs as key regulators of gametophore apical cells downstream of cytokinin. Given that ESRs promote SAM formation under cytokinin in angiosperms, we propose that the cytokinin-ESR module represents a conserved mechanism promoting stem cell identity that evolved in the common ancestor of land plants.

plant biology↗

bioRxiv2023

Cytokinins specify pluripotent stem cell identity in the moss Physcomitrium patens

The shoot apical meristem (SAM) contains pluripotent stem cells that produce all the aerial parts of the plant. Stem cells undergo asymmetric cell divisions to self-renew and to produce differentiating cells. Our research focused on unraveling the mechanisms governing the specification of these two distinct cell fates following the stem cell division. For this purpose, we used the model organism Physcomitrium patens, which features a singular pluripotent stem cell known as the gametophore apical cell. We show that the activity of cytokinins, critical stem cell regulators, is restricted to the gametophore apical cell due to the specific localization of PpLOG, the enzyme responsible of cytokinin activation. In turn, PpTAW, which promotes differentiating cell identity of the merophyte, is excluded from the gametophore apical cell by the action of cytokinins. We propose a cytokinin-based model for the establishment of asymmetry in the pluripotent stem cell division. One Sentence SummaryCytokinins are confined to the pluripotent stem cells and exclude the differentiation factor TAW1 to establish the SAM from a single stem cell.

plant biology↗

bioRxiv2023

The transcriptional changes underlying the flowering phenology shift in response to climate warming

Climate warming is causing shifts in key life-history events, such as flowering time. To assess the impacts of climate warming on flowering phenology, it is crucial to understand the transcriptional changes of genes underlying the phenological shifts. Here, we comprehensively explore genes that contribute to the flowering phenology shifts under climate warming by monitoring the latitudinal gradient of seasonal expression dynamics of 293 flowering-time genes in a perennial herb, Arabidopsis halleri. Through transplant experiments conducted at northern, southern, and subtropical study sites in Japan, we have demonstrated that the flowering period was shortened with decreasing latitude and ultimately, the plants lost the opportunity to flower in subtropical climates. The key transcriptional changes underlying the shift in flowering phenology and the loss of flowering opportunity were the diminished expression of floral pathway integrator genes and genes in the gibberellin synthesis and aging pathways, all of which are suppressed by increased expression of FLOWERING LOCUS C, a central repressor of flowering. These results suggest that the upper-temperature threshold beyond which plants cannot reproduce in response to warming is governed by a relatively small number of genes that suppress reproduction in the absence of winter cold.

plant biology↗

bioRxiv2021

The first transchromosomic rat model with human chromosome 21 shows robust Down syndrome features

Progress in earlier detection and symptom management has increased life expectancy and quality of life in people with Down syndrome (DS). However, no drug has been approved to help individuals with DS live independently and fully. Although rat models could support more robust physiological, behavioral, and toxicology analysis than mouse models during preclinical validation, no DS rat model is available due to technical challenges. We developed the first transchromosomic rat model of DS, TcHSA21rat, which contains a freely segregating, EGFP-inserted, human chromosome 21 (HSA21) with >93% of its protein coding genes. RNA-Seq of neonatal forebrains demonstrates that TcHSA21rat not only expresses HSA21 genes but also has an imbalance in global gene expression. Using EGFP as a marker for trisomic cells, flow cytometry analyses of peripheral blood cells from 361 adult TcHSA21rat animals show that 81% of animals retain HSA21 in >80% of cells, the criterion for a "Down syndrome karyotype" in people. TcHSA21rat exhibits learning and memory deficits and shows increased anxiety and hyperactivity. TcHSA21rat recapitulates well-characterized DS brain morphology, including smaller brain volume and reduced cerebellar size. In addition, the rat model shows reduced cerebellar foliation, a prominent feature of DS that is not observed in DS mouse models. Moreover, TcHSA21rat exhibits anomalies in craniofacial morphology, heart development, husbandry, and stature. TcHSA21rat is a robust DS animal model that can facilitate DS basic research and provide a unique tool for preclinical validation to accelerate DS drug development.

genetics↗

bioRxiv2021

Functional cortical localization of the tongue using corticokinematic coherence with a deep learning-assisted motion capture system

Measuring the corticokinematic coherence (CKC) between magnetoencephalographic and movement signals using an accelerometer can evaluate the functional localization of the primary sensorimotor cortex (SM1) of the upper limbs. However, it is difficult to determine the tongue CKC because an accelerometer yields excessive magnetic artifacts. We introduce and validate a novel approach for measuring the tongue CKC using a deep learning-assisted motion capture system with videography, and compare it with an accelerometer in a control task measuring finger movement. Twelve healthy volunteers performed rhythmical side-to-side tongue movements in the whole-head magnetoencephalographic system, which were simultaneously recorded using a video camera and examined offline using a deep learning-assisted motion capture system. In the control task, right finger CKC measurements were simultaneously evaluated via motion capture and an accelerometer. The right finger CKC with motion capture was significant at the movement frequency peaks or its harmonics over the contralateral hemisphere; the motion-captured CKC was 84.9% similar to that with the accelerometer. The tongue CKC was significant at the movement frequency peaks or its harmonics over both hemispheres, with no difference between the left and right hemispheres. The CKC sources of the tongue were considerably lateral and inferior to those of the finger. Thus, the CKC based on deep learning-assisted motion capture can evaluate the functional localization of the tongue SM1. In this approach, because no devices are placed on the tongue, magnetic noise, disturbances due to tongue movements, risk of aspiration of the device, and risk of infection to the experimenter are eliminated.

neuroscience↗

bioRxiv2020

Molecular interaction mechanism of 14-3-3ε protein with phosphorylated Myeloid leukemia factor 1 revealed by an enhanced conformational sampling

Enhanced conformational sampling, a genetic-algorithm-guided multi-dimensional virtual-system coupled molecular dynamics, can provide equilibrated conformational distributions of a receptor protein and a flexible ligand at room temperature. The distributions provide not only the most stable but also semi-stable complex structures, and propose a ligand-receptor binding process. This method was applied to a system consisting of a receptor protein, 14-3-3{varepsilon}, and a flexible peptide, phosphorylated Myeloid leukemia factor 1 (pMLF1). The results present comprehensive binding pathways of pMLF1 to 14-3-3{varepsilon}. We identified four thermodynamically stable clusters of MLF1 on the 14-3-3{varepsilon} surface, and free-energy barriers among some clusters. The most stable cluster includes two high-density spots connected by a narrow corridor. When pMLF1 passes the corridor, a salt-bridge relay (switching) related to the phosphorylated residue of pMLF1 occurs. Conformations in one high-density spots are similar to the experimentally determined complex structure. Three-dimensional distributions of residues in the intermolecular interface rationally explain the binding-constant changes resultant from alanine-mutation experiment for the residues. We performed a simulation of non-phosphorylated peptide and 14-3-3{varepsilon}, which demonstrated that the complex structure was unstable, suggesting that phosphorylation of the peptide is crucially important for binding to 14-3-3{varepsilon}.

biophysics↗

bioRxiv2018

The potential aroma and flavor compounds in Vitis sp. cv. Koshu and V. vinifera L. cv. Chardonnay under different environmental conditions

ABSTRACTO_ST_ABSBACKGROUNDC_ST_ABSKoshu, a hybrid of Vitis vinifera L. and V. davidii Foex, is the most popular indigenous cultivar for wine production in Japan. However, little is known about the potential aroma compounds it contains and how environmental factors affect these. In this study, we obtained comprehensive profiles of the volatile (both glycosidically bound and free) and phenolic compounds that occur in Koshu berries, and compared these with similar profiles for V. vinifera cv. Chardonnay. We then compared the response of these two cultivars to bunch shading and the ripening-related phytohormone abscisic acid (ABA).\n\nRESULTSKoshu berries contained significantly higher concentrations of phenolic compounds, hydroxycinnamic acid derivatives, and some volatile phenols, such as 4-vinyl guaiacol and eugenol, than Chardonnay berries, which are thought to contribute to the characteristics of Koshu wine. In addition, Koshu berries had a distinctly different terpenoid composition from Chardonnay berries. Shading reduced the concentrations of norisoprenoid in both cultivars, as well as several phenolic compounds particularly their volatile derivatives in Koshu. The exogenous application of ABA induced ripening and increased the concentrations of lipid derivatives, such ashexanol, octanol, nonanol, and 1-octen-3-ol. Linear discriminant analysis showed that the aromatic potential could be discriminated clearly based on cultivar, bunch shading, and ABA application.\n\nCONCLUSIONThe unique secondary metabolite profiles of Koshu and their different responses to environmental factors could be valuable for developing various styles of Koshu wines and new cultivars with improved quality and cultural characteristics.

plant biology↗

bioRxiv2018

The RASSF6 tumor suppressor protein regulates apoptosis and cell cycle progression via Retinoblastoma protein.

RASSF6 is a member of the tumor suppressor Ras-association domain family (RASSF) proteins. RASSF6 is frequently suppressed in human cancers and its low expression is associated with poor prognosis. RASSF6 regulates cell cycle arrest and apoptosis and plays a tumor suppressor role. Mechanistically, RASSF6 blocks MDM2-mediated p53 degradation and enhances p53 expression. However, RASSF6 also induces cell cycle arrest and apoptosis in the p53-negative background, which implies that the tumor suppressor function of RASSF6 does not depend solely on p53. In this study, we have revealed that RASSF6 mediates cell cycle arrest and apoptosis via pRb. RASSF6 enhances the interaction between pRb and protein phosphatase. RASSF6 also enhances P16INK4A and P14ARF expression through suppressing BMI1. In this way, RASSF6 increases unphosphorylated pRb and augments the interaction between pRb and E2F1. Moreover, RASSF6 induces TP73-target genes via pRb and E2F1 in the p53-negative background. Finally, we confirmed that RASSF6 depletion induces polypoid cells in p53-negative HCT116 cells. In conclusion, RASSF6 behaves as a tumor suppressor in cancers with the loss-of-function of p53, and pRb is implicated in this function of RASSF6.

molecular biology↗