Tokushima University / Educator and Researcher Directory --- Watanabe, Takahito

Personal Web Page

https://researchmap.jp/TakahitoWatanabe (researchmap)

Field of Study

○	Life sciences [Zoological sciences]
○	Life sciences [Developmental biology]
○	Life sciences [Molecular biology]

Subject of Study

Book / Paper

(See https://researchmap.jp/TakahitoWatanabe (researchmap) for Published Book / Papers / Presentations.)

Book:

1.	Takahito Watanabe : 昆虫食の社会実装に向けた課題, Nov. 2022.
2.	Takahito Watanabe : 食用コオロギを活用した循環型食品の研究開発と事業化, Jul. 2022.
3.	Takahito Watanabe : 食品と開発「循環型食品``サーキュラーフード''の推進」, インフォーママーケッツジャパン株式会社, Jan. 2022.
4.	Takahito Watanabe, 岡部慎司 and Taro Mito : 『代替タンパク質の現状と社会実装へ向けた取り組み』第6章第2節食用コオロギの生産と商品展開, 情報機構, Nov. 2021.
5.	Takahito Watanabe and Taro Mito : 『「代替プロテイン」 ∼植物肉製品の開発，昆虫・藻類の食品素材利用と培養肉の作製∼』第3篇第1章第1節，ゲノム編集による食用コオロギの品種改良技術, NTS Inc., Jul. 2021.
6.	Takahito Watanabe and 岡部慎司 : 『「代替プロテイン」 ∼植物肉製品の開発，昆虫・藻類の食品素材利用と培養肉の作製∼』第3篇第2章第1節，食用コオロギの飼育と食品への応用, NTS Inc., Jul. 2021.
7.	Takahito Watanabe : 『フードテックの最新動向』第13章，循環型タンパク質としての食用コオロギの飼育と食品への応用, 株式会社シーエムシー出版, Jul. 2021.
8.	Taro Mito, Takahito Watanabe and 岡部慎司 : 宇宙ビジネス新規参入の手引き, 情報機構, 東京, Sep. 2020.
9.	Takahito Watanabe, Sumihare Noji and Taro Mito : GeneKnockout by Targeted Mutagenesis in a Hemimetabolous Insect, the Two-Spotted Cricket Gryllus bimaculatus, using TALENs. In TALENs: Methods and Protocols (Ralf Kuhn et al. eds.), Springer, New York, 2016. (Link to Publication Site) ● Publication site (DOI): 10.1007/978-1-4939-2932-0_12 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1007/978-1-4939-2932-0_12 (DOI: 10.1007/978-1-4939-2932-0_12)
10.	Takahito Watanabe, 松岡佑児, Sumihare Noji and Taro Mito : 進化するゲノム編集技術(真下知士, 城石俊彦監修)第2編第2章第4節フタホシコオロギにおけるゲノム編集, エヌ・ティー・エス, Jan. 2015.
11.	Takahito Watanabe, Taro Mito, Hideyo Ohuchi and Sumihare Noji : 第10章コオロギにおけるZFN，TALEN，CRISPR/Cas9を用いた遺伝子改変, 羊土社, Apr. 2014.

Academic Paper (Judged Full Paper):

1.	Aya Nakai, Shiho Fukushima, Kazuaki Mawatari, Akira Takahashi, Takeshi Nikawa, Shintaro Inoue, Takahito Watanabe, Taro Mito and Katsuyuki Miyawaki : Differential Expression of Key Isoflavone Synthesis Genes in Soybean Sprouts under Two LED Treatments, ACS Agricultural Science & Technology, 2025. (Summary) Soybean seeds and sprouts contain isoflavones, including aglycones, glucosides, and malonylated glucosides, and their contents vary across soybean varieties. During germination and photomorphogenesis, blue light-emitting diode (LED) irradiation suppressed hypocotyl growth and enhanced the expression levels of chalcone synthase 7, isoflavone synthase (IFS), and isoflavone reductase (IFR). Conversely, red LED irradiation enhanced hypocotyl growth and decreased the expression levels of IFS and IFR. The contents of some glycosides or malonylated glycosides in sprouts and young green soybeans were significantly higher under blue LED irradiation than under red LED irradiation. These results imply that blue light more effectively increased the concentrations of some isoflavones during early germination and/or hydroponics cultivation. (Link to Publication Site) ● Publication site (DOI): 10.1021/acsagscitech.4c00646 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1021/acsagscitech.4c00646 (DOI: 10.1021/acsagscitech.4c00646)
2.	Kohei Kawamoto, Yoshiyasu Ishimaru, Sayuri Tomonari, Takahito Watanabe, Sumihare Noji and Taro Mito : Myoglianin is a crucial factor for the transition to the juvenile hormone-dependent phase during hemimetabolous nymphal development., Insect Biochemistry and Molecular Biology, 178, 104274, 2025. (Summary) In hemimetabolous insects, the developmental process of nymphs is divided into three growth phases, i.e., juvenile hormone (JH)-independent, JH-dependent, and JH-free phases. The wing primordium in hemimetabolous insects is formed latently in the JH-independent phase and manifests and grows in the JH-dependent phase. Myoglianin (Myo) is known to be a key factor of metamorphosis in the JH-free phase of nymphs, regulating negatively JH synthesis. Here we find the role of Myo in earlier phases in the cricket Gryllus bimaculatus via gene knockout analysis using CRISPR/Cas9. In the myo knockout (KO) mutants, developmental delay during embryogenesis was observed, and nymphal body size and the timing of molting were affected. The KO nymphs underwent multiple molts, typically around seven, but remained significantly smaller in body size compared to wild-type individuals. The KO nymphs also did not exhibit the expected growth of wing primordia, implying that transition to JH-dependent phase was failed. This failure in phase transition could have been caused by excessive JH because titers of JH I and JH II were remarkably increased in the KO mutants. Our results suggest that Myo plays a crucial role not only in regulating timing of molting but also in the transition to the nymphal growth phases associated with growth of wing primordia and nymphal body size. (Keyword) Animals / Nymph / Juvenile Hormones / Molting / Gryllidae / Insect Proteins / Wings, Animal / Metamorphosis, Biological / Gene Knockout Techniques (Link to Publication Site) ● Publication site (DOI): 10.1016/j.ibmb.2025.104274 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 39947524 ● Search Scopus @ Elsevier (PMID): 39947524 ● Search Scopus @ Elsevier (DOI): 10.1016/j.ibmb.2025.104274 (DOI: 10.1016/j.ibmb.2025.104274, PubMed: 39947524)
3.	Shintaro Inoue, Kai Fujie, Taiki Hamaguchi, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Akira Takahashi, Takeshi Nikawa, Sumihare Noji, Takahito Watanabe and Taro Mito : Lineage-specific duplication and functional diversification of DOPA-decarboxylase genes in the Gryllidae family, as revealed in Gryllus bimaculatus., Insect Biochemistry and Molecular Biology, 177, 104246, 2025. (Summary) The DOPA-decarboxylase (DDC) gene is crucial for dopamine synthesis and influences various biological functions in insects, including body coloration, behavior, learning, and sleep. However, its evolutionary impact remains largely unexplored. This study reports on the tandem duplication of two bona fide ddc genes (ddc1 and ddc2) in the Gryllidae cricket family. We herein investigated the function of ddc1 and ddc2 using Gryllus bimaculatus (Gb) as a model. Our results revealed that Gb'ddc1 was expressed systemically, with its expression being higher immediately after molting compared to the stage following melanin pigmentation. In homozygous knockout mutants of Gb'ddc1, generated via CRISPR/Cas9, reduced body color pigmentation and had translucent cuticles, decreased dopamine levels, and over-accumulated DOPA. These mutants died shortly after hatching, likely due to cuticle defects, underscoring the essential role of dopamine, produced by Gb'ddc1, in melanin synthesis. Conversely, Gb'ddc2 expression was confined to the ovary and was not up-regulated after molting. Homozygous knockout mutants of Gb'ddc2 exhibited no body color defects, whereas hatchability and embryonic development rates were significantly reduced. Interestingly, dopamine levels in the ovaries were significantly elevated in Gb'ddc2 mutants. This suggests that normal ovarian dopamine levels, modulated by Gb'ddc2, are vital for fertility maintenance. The function of Gb'ddc2 differs from that of typical ddc, indicating neofunctionalization through evolutionary duplication. Overall, Gb'ddc1 and Gb'ddc2 have distinct functions, and precise regulation of ovarian dopamine levels using these two ddc genes may have enhanced cricket fertility. (Link to Publication Site) ● Publication site (DOI): 10.1016/j.ibmb.2024.104246 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 39653316 ● Search Scopus @ Elsevier (PMID): 39653316 ● Search Scopus @ Elsevier (DOI): 10.1016/j.ibmb.2024.104246 (DOI: 10.1016/j.ibmb.2024.104246, PubMed: 39653316)
4.	Yuji Matsuoka, Taro Nakamura, Takahito Watanabe, Austen A Barnett, Sayuri Tomonari, Guillem Ylla, Carrie A Whittle, Sumihare Noji, Taro Mito and Cassandra G Extavour : Establishment of CRISPR/Cas9-based knock-in in a hemimetabolous insect: targeted gene tagging in the cricket Gryllus bimaculatus, Development, 152, 1, dev199746, 2025. (Summary) Studies of traditional model organisms such as the fruit fly Drosophila melanogaster have contributed immensely to our understanding of the genetic basis of developmental processes. However, the generalizability of these findings cannot be confirmed without functional genetic analyses in additional organisms. Direct genome editing using targeted nucleases has the potential to transform hitherto poorly understood organisms into viable laboratory organisms for functional genetic study. To this end, we present a method to induce targeted genome knockout and knock-in of desired sequences in an insect that serves as an informative contrast to Drosophila, the cricket Gryllus bimaculatus. The efficiency of germline transmission of induced mutations is comparable with that reported for other well-studied laboratory organisms, and knock-ins targeting introns yield viable, fertile animals in which knock-in events are directly detectable by visualization of a fluorescent marker in the expression pattern of the targeted gene. Combined with the recently assembled and annotated genome of this cricket, this knock-in/knockout method increases the viability of G. bimaculatus as a tractable system for functional genetics in a basally branching insect. (Keyword) Animals / Gryllidae / CRISPR-Cas Systems / Gene Knock-In Techniques / Gene Editing / Male / Genome, Insect / Female / Gene Knockout Techniques (Tokushima University Institutional Repository) ● Metadata: 2013304 (Link to Publication Site) ● Publication site (DOI): 10.1242/dev.199746 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 39514640 ● Summary page in Scopus @ Elsevier: 2-s2.0-85215148311 (Tokushima University Institutional Repository: 2013304, DOI: 10.1242/dev.199746, PubMed: 39514640, Elsevier: Scopus)
5.	Takahisa Yamashita, Takahiro Ohde, Taro Nakamura, Yoshiyasu Ishimaru, Takahito Watanabe, Sayuri Tomonari, Yuki Nakamura, Sumihare Noji and Taro Mito : Involvement of the scalloped gene in morphogenesis of the wing margin via regulating cell growth in a hemimetabolous insect Gryllus bimaculatus., Development Growth & Differentiation, 65, 6, 348-359, 2023. (Summary) The acquisition of wings was a key event in insect evolution. As hemimetabolous insects were the first group to acquire functional wings, establishing the mechanisms of wing formation in this group could provide useful insights into their evolution. In this study, we aimed to elucidate the expression and function of the gene scalloped (sd), which is involved in wing formation in Drosophila melanogaster, and in Gryllus bimaculatus mainly during postembryonic development. Expression analysis showed that sd is expressed in the tergal edge, legs, antennae, labrum, and cerci during embryogenesis and in the distal margin of the wing pads from at least the sixth instar in the mid to late stages. Because sd knockout caused early lethality, nymphal RNA interference experiments were performed. Malformations were observed in the wings, ovipositor, and antennae. By analyzing the effects on wing morphology, it was revealed that sd is mainly involved in the formation of the margin, possibly through the regulation of cell proliferation. In conclusion, sd might regulate the local growth of wing pads and influence wing margin morphology in Gryllus. (Keyword) Animals / Cell Cycle / Cell Proliferation / Embryonic Development / Insect Proteins / Wings, Animal / Gryllidae / Transcription Factors (Link to Publication Site) ● Publication site (DOI): 10.1111/dgd.12869 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 37310211 ● Summary page in Scopus @ Elsevier: 2-s2.0-85162895470 (DOI: 10.1111/dgd.12869, PubMed: 37310211, Elsevier: Scopus)
6.	Shintaro Inoue, Takahito Watanabe, Taiki Hamaguchi, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Takeshi Nikawa, Akira Takahashi, Sumihare Noji and Taro Mito : Combinatorial expression of ebony and tan generates body color variation from nymph through adult stages in the cricket, Gryllus bimaculatus., PLoS ONE, 18, 5, 2023. (Summary) Insect body colors and patterns change markedly during development in some species as they adapt to their surroundings. The contribution of melanin and sclerotin pigments, both of which are synthesized from dopamine, to cuticle tanning has been well studied. Nevertheless, little is known about how insects alter their body color patterns. To investigate this mechanism, the cricket Gryllus bimaculatus, whose body color patterns change during postembryonic development, was used as a model in this study. We focused on the ebony and tan genes, which encode enzymes that catalyze the synthesis and degradation, respectively, of the precursor of yellow sclerotin N-β-alanyl dopamine (NBAD). Expression of the G. bimaculatus (Gb) ebony and tan transcripts tended to be elevated just after hatching and the molting period. We found that dynamic alterations in the combined expression levels of Gb'ebony and Gb'tan correlated with the body color transition from the nymphal stages to the adult. The body color of Gb'ebony knockout mutants generated by CRISPR/Cas9 systemically darkened. Meanwhile, Gb'tan knockout mutants displayed a yellow color in certain areas and stages. The phenotypes of the Gb'ebony and Gb'tan mutants probably result from an over-production of melanin and yellow sclerotin NBAD, respectively. Overall, stage-specific body color patterns in the postembryonic stages of the cricket are governed by the combinatorial expression of Gb'ebony and Gb'tan. Our findings provide insights into the mechanism by which insects evolve adaptive body coloration at each developmental stage. (Keyword) Animals / Melanins / Gryllidae / Nymph / dopamine / Insect Proteins (Tokushima University Institutional Repository) ● Metadata: 2011711 (Link to Publication Site) ● Publication site (DOI): 10.1371/journal.pone.0285934 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 37200362 ● Search Scopus @ Elsevier (PMID): 37200362 ● Search Scopus @ Elsevier (DOI): 10.1371/journal.pone.0285934 (Tokushima University Institutional Repository: 2011711, DOI: 10.1371/journal.pone.0285934, PubMed: 37200362)
7.	Yuki Nakamura, Sayuri Tomonari, Kohei Kawamoto, Takahisa Yamashita, Takahito Watanabe, Yoshiyasu Ishimaru, Sumihare Noji and Taro Mito : Evolutionarily conserved function of the even-skipped ortholog in insects revealed by gene knock-out analyses in Gryllus bimaculatus., Developmental Biology, 485, 1-8, 2022. (Summary) Comparing the developmental mechanisms of segmentation among insects with different modes of embryogenesis provides insights on how the function of segmentation genes evolved. Functional analysis of eve by genetic mutants shows that the Drosophila pair-rule gene, even-skipped (eve), contributes to initial segmental patterning. However, eve orthologs tends to have diverse functions in other insects. To compare the evolutionary functional divergence of this gene, we evaluated eve function in a phylogenetically basal insect, the cricket Gryllus bimaculatus. To investigate the phenotypic effects of eve gene knock-out, we generated CRISPR/Cas9 system-mediated mutant strains of the cricket. CRISPR/Cas9 mutagenesis of multiple independent sites in the eve coding region revealed that eve null mutant embryos were defective in forming the gnathal, thoracic, and abdominal segments, consequently shortening the anterior-posterior axis. In contrast, the structures of the anterior and posterior ends (e.g., antenna, labrum, and cercus) formed normally. Hox gene expression in the gnathal, thoracic, and abdominal segments was detected in the mutant embryos. Overall, this study showed that Gryllus eve plays an important role in embryonic elongation and the formation of segmental boundaries in the gnathal to abdominal region of crickets. In the light of studies on other species, the eve function shown in Gryllus might be ancestral in insects. (Keyword) Amino Acid Sequence / Animals / Body Patterning / Drosophila / Drosophila Proteins / Gene Expression Regulation, Developmental / Gryllidae / Homeodomain Proteins / Insecta / RNA Interference / Transcription Factors (Link to Publication Site) ● Publication site (DOI): 10.1016/j.ydbio.2022.02.005 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 35196518 ● Search Scopus @ Elsevier (PMID): 35196518 ● Search Scopus @ Elsevier (DOI): 10.1016/j.ydbio.2022.02.005 (DOI: 10.1016/j.ydbio.2022.02.005, PubMed: 35196518)
8.	Guillem Ylla, Taro Nakamura, Takehiko Itoh, Rei Kajitani, Atsushi Toyoda, Sayuri Tomonari, Tetsuya Bando, Yoshiyasu Ishimaru, Takahito Watanabe, Masao Fuketa, Yuji Matsuoka, A Austen Barnett, Sumihare Noji, Taro Mito and G Cassandra Extavour : Insights into the genomic evolution of insects from cricket genomes., Communications Biology, 4, 1, 2021. (Summary) Most of our knowledge of insect genomes comes from Holometabolous species, which undergo complete metamorphosis and have genomes typically under 2 Gb with little signs of DNA methylation. In contrast, Hemimetabolous insects undergo the presumed ancestral process of incomplete metamorphosis, and have larger genomes with high levels of DNA methylation. Hemimetabolous species from the Orthopteran order (grasshoppers and crickets) have some of the largest known insect genomes. What drives the evolution of these unusual insect genome sizes, remains unknown. Here we report the sequencing, assembly and annotation of the 1.66-Gb genome of the Mediterranean field cricket Gryllus bimaculatus, and the annotation of the 1.60-Gb genome of the Hawaiian cricket Laupala kohalensis. We compare these two cricket genomes with those of 14 additional insects and find evidence that hemimetabolous genomes expanded due to transposable element activity. Based on the ratio of observed to expected CpG sites, we find higher conservation and stronger purifying selection of methylated genes than non-methylated genes. Finally, our analysis suggests an expansion of the pickpocket class V gene family in crickets, which we speculate might play a role in the evolution of cricket courtship, including their characteristic chirping. (Keyword) Animals / DNA Methylation / DNA Transposable Elements / Evolution, Molecular / Female / Genes, Insect / Genome, Insect / Gryllidae / Insecta / Male / Phylogeny / Repetitive Sequences, Nucleic Acid / Sequence Analysis, DNA (Tokushima University Institutional Repository) ● Metadata: 2009776 (Link to Publication Site) ● Publication site (DOI): 10.1038/s42003-021-02197-9 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 34127782 ● Search Scopus @ Elsevier (PMID): 34127782 ● Search Scopus @ Elsevier (DOI): 10.1038/s42003-021-02197-9 (Tokushima University Institutional Repository: 2009776, DOI: 10.1038/s42003-021-02197-9, PubMed: 34127782)
9.	Aya Nakai, Akihito Tanaka, Hitoshi Yoshihara, Koji Murai, Takahito Watanabe and Katsuyuki Miyawaki : Blue LED light promotes indican accumulation and flowering in indigo plant, Polygonum tinctorium, Industrial Crops and Products, 155, 112774, 2020. (Keyword) Polygonum tinctorium / Plant factory / Blue LED / Photoperiod / Flowering / Indican (Tokushima University Institutional Repository) ● Metadata: 2007922 (Link to Publication Site) ● Publication site (DOI): 10.1016/j.indcrop.2020.112774 (Link to Search Site for Scientific Articles) ● Summary page in Scopus @ Elsevier: 2-s2.0-85088149064 (Tokushima University Institutional Repository: 2007922, DOI: 10.1016/j.indcrop.2020.112774, Elsevier: Scopus)
10.	Yoshiyasu Ishimaru, Sayuri Tomonari, Takahito Watanabe, Sumihare Noji and Taro Mito : Regulatory mechanisms underlying the specification of the pupal-homologous stage in a hemimetabolous insect, Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 374, 1783, 20190225, 2019. (Summary) Juvenile hormones and the genetic interaction between the transcription factors Krüppel homologue 1 (Kr-h1) and Broad (Br) regulate the transformation of insects from immature to adult forms in both types of metamorphosis (holometaboly with a pupal stage versus hemimetaboly with no pupal stage); however, knowledge about the exact instar in which this occurs is limited. Using the hemimetabolous cricket Gryllus bimaculatus (Gb), we demonstrate that a genetic interaction occurs among Gb'Kr-h1, Gb'Br and the adult-specifier transcription factor Gb'E93 from the sixth to final (eighth) nymphal instar. Gb'Kr-h1 and Gb'Br mRNAs were strongly expressed in the abdominal tissues of sixth instar nymphs, with precocious adult moults being induced by Gb'Kr-h1 or Gb'Br knockdown in the sixth instar. The depletion of Gb'Kr-h1 or Gb'Br upregulates Gb'E93 in the sixth instar. By contrast, Gb'E93 knockdown at the sixth instar prevents nymphs transitioning to adults, instead producing supernumerary nymphs. Gb'E93 also represses Gb'Kr-h1 and Gb'Br expression in the penultimate nymphal instar, demonstrating its important role in adult differentiation. Our results suggest that the regulatory mechanisms underlying the pupal transition in holometabolous insects are evolutionarily conserved in hemimetabolous G. bimaculatus, with the penultimate and final nymphal periods being equivalent to the pupal stage. This article is part of the theme issue 'The evolution of complete metamorphosis'. (Tokushima University Institutional Repository) ● Metadata: 2006718 (Link to Publication Site) ● Publication site (DOI): 10.1098/rstb.2019.0225 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 31438810 ● Search Scopus @ Elsevier (PMID): 31438810 ● Search Scopus @ Elsevier (DOI): 10.1098/rstb.2019.0225 (Tokushima University Institutional Repository: 2006718, DOI: 10.1098/rstb.2019.0225, PubMed: 31438810)
11.	Kamenura Norio, Mayumi Sugimoto, Tamehiro Norimasa, Adachi Reiko, Sayuri Tomonari, Takahito Watanabe and Taro Mito : Cross-allergenicity of crustacean and the edible insect Gryllus bimaculatus in patients with shrimp allergy, Molecular Immunology, 106, 127-134, 2019. (Summary) Food scarcity is a serious problem for many developing as well as developed countries. Edible insects have attracted attention recently as a novel food source. Crickets are especially high in nutritional value and easy to breed and harvest. In this study, we evaluated the risk of allergic reactions associated with cricket consumption in individuals with crustacean allergy. We evaluated food allergy risk in the consumption of Gryllus bimaculatus (cricket) in patients with shrimp allergy, using enzyme-linked immunosorbent assay (ELISA) and IgE crosslinking-induced luciferase expression assay (EXiLE). Sera from individuals with shrimp allergy (positive for shrimp-specific IgE by ImmunoCAP (>0.35 UA/mL; n = 9) or without shrimp allergy (negative for shrimp-specific IgE; n = 6) were obtained. There was a strong correlation between shrimp- and Gryllus-specific IgE levels obtained by ELISA (r = 0.99; P < 0.001). The binding of shrimp-specific IgE on shrimp allergen was dose-dependently inhibited by Gryllus allergen (0-1.0 mg/mL). There was a strong correlation between shrimp- and Gryllus-specific IgE responses, as assessed by EXiLE assays (r = 0.89; P < 0.001). We determined that a protein of approximately 40 kDa reacted with the positive, but not negative, sera for shrimp-specific IgE by ImmunoCAP. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis identified the major allergen in shrimp and Gryllus to be tropomyosin. Our data suggest that the cricket allergen has the potential to induce an allergic reaction in individuals with crustacean allergy. Therefore, allergy risk and shrimp-specific IgE levels should be considered before consumption of cricket meal. (Keyword) Adolescent / Adult / Allergens / Animals / Child / Child, Preschool / Cross Reactions / Female / Gryllidae / Humans / Immunoglobulin E / Male / Shellfish / Shellfish Hypersensitivity (Link to Publication Site) ● Publication site (DOI): 10.1016/j.molimm.2018.12.015 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 30597474 ● Search Scopus @ Elsevier (PMID): 30597474 ● Search Scopus @ Elsevier (DOI): 10.1016/j.molimm.2018.12.015 (DOI: 10.1016/j.molimm.2018.12.015, PubMed: 30597474)
12.	Risa Ueta, Chihiro Abe, Ryosuke Ishihara, Takahito Watanabe, Sigeo Sugano, Hiroshi Ezura, Yuriko Osakabe and Keishi Osakabe : Rapid breeding of parthenocarpic tomato plants using CRISPR/Cas9., Scientific Reports, 7, 507, 2017. (Summary) Parthenocarpy in horticultural crop plants is an important trait with agricultural value for various industrial purposes as well as direct eating quality. Here, we demonstrate a breeding strategy to generate parthenocarpic tomato plants using the CRISPR/Cas9 system. We optimized the CRISPR/Cas9 system to introduce somatic mutations effectively into SlIAA9-a key gene controlling parthenocarpy-with mutation rates of up to 100% in the T0 generation. Furthermore, analysis of off-target mutations using deep sequencing indicated that our customized gRNAs induced no additional mutations in the host genome. Regenerated mutants exhibited morphological changes in leaf shape and seedless fruit-a characteristic of parthenocarpic tomato. And the segregated next generation (T1) also showed a severe phenotype associated with the homozygous mutated genome. The system developed here could be applied to produce parthenocarpic tomato in a wide variety of cultivars, as well as other major horticultural crops, using this precise and rapid breeding technique. (Tokushima University Institutional Repository) ● Metadata: 2003363 (Link to Publication Site) ● Publication site (DOI): 10.1038/s41598-017-00501-4 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 28360425 ● Summary page in Scopus @ Elsevier: 2-s2.0-85016547132 ● Summary page in Scopus @ Elsevier: 2-s2.0-85091785997 (Tokushima University Institutional Repository: 2003363, DOI: 10.1038/s41598-017-00501-4, PubMed: 28360425, Elsevier: Scopus, Elsevier: Scopus)
13.	Yuriko Osakabe, Takahito Watanabe, SS Sugano, R Ueta, R Ishihara, K Shinozaki and Keishi Osakabe : Optimization of CRISPR/Cas9 genome editing to modify abiotic stress responses in plants., Scientific Reports, 6, 26685, 2016. (Summary) Genome editing using the CRISPR/Cas9 system can be used to modify plant genomes, however, improvements in specificity and applicability are still needed in order for the editing technique to be useful in various plant species. Here, using genome editing mediated by a truncated gRNA (tru-gRNA)/Cas9 combination, we generated new alleles for OST2, a proton pump in Arabidopsis, with no off-target effects. By following expression of Cas9 and the tru-gRNAs, newly generated mutations in CRIPSR/Cas9 transgenic plants were detected with high average mutation rates of up to 32.8% and no off-target effects using constitutive promoter. Reducing nuclear localization signals in Cas9 decreased the mutation rate. In contrast, tru-gRNA Cas9 cassettes driven by meristematic- and reproductive-tissue-specific promoters increased the heritable mutation rate in Arabidopsis, showing that high expression in the germ line can produce bi-allelic mutations. Finally, the new mutant alleles obtained for OST2 exhibited altered stomatal closing in response to environmental conditions. These results suggest further applications in molecular breeding to improve plant function using optimized plant CRISPR/Cas9 systems. (Tokushima University Institutional Repository) ● Metadata: 2003352 (Link to Publication Site) ● Publication site (DOI): 10.1038/srep26685 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 27226176 ● Summary page in Scopus @ Elsevier: 2-s2.0-84971280492 (Tokushima University Institutional Repository: 2003352, DOI: 10.1038/srep26685, PubMed: 27226176, Elsevier: Scopus)
14.	Yoshiyasu Ishimaru, Sayuri Tomonari, Yuji Matsuoka, Takahito Watanabe, Katsuyuki Miyawaki, Tetsuya Bando, Kenji Tomioka, Hideyo Ohuchi, Sumihare Noji and Taro Mito : TGF-β signaling in insects regulates metamorphosis via juvenile hormone biosynthesis., Proceedings of the National Academy of Sciences of the United States of America, 113, 20, 5634-5639, 2016. (Summary) Although butterflies undergo a dramatic morphological transformation from larva to adult via a pupal stage (holometamorphosis), crickets undergo a metamorphosis from nymph to adult without formation of a pupa (hemimetamorphosis). Despite these differences, both processes are regulated by common mechanisms that involve 20-hydroxyecdysone (20E) and juvenile hormone (JH). JH regulates many aspects of insect physiology, such as development, reproduction, diapause, and metamorphosis. Consequently, strict regulation of JH levels is crucial throughout an insect's life cycle. However, it remains unclear how JH synthesis is regulated. Here, we report that in the corpora allata of the cricket, Gryllus bimaculatus, Myoglianin (Gb'Myo), a homolog of Drosophila Myoglianin/vertebrate GDF8/11, is involved in the down-regulation of JH production by suppressing the expression of a gene encoding JH acid O-methyltransferase, Gb'jhamt In contrast, JH production is up-regulated by Decapentaplegic (Gb'Dpp) and Glass-bottom boat/60A (Gb'Gbb) signaling that occurs as part of the transcriptional activation of Gb'jhamt Gb'Myo defines the nature of each developmental transition by regulating JH titer and the interactions between JH and 20E. When Gb'myo expression is suppressed, the activation of Gb'jhamt expression and secretion of 20E induce molting, thereby leading to the next instar before the last nymphal instar. Conversely, high Gb'myo expression induces metamorphosis during the last nymphal instar through the cessation of JH synthesis. Gb'myo also regulates final insect size. Because Myo/GDF8/11 and Dpp/bone morphogenetic protein (BMP)2/4-Gbb/BMP5-8 are conserved in both invertebrates and vertebrates, the present findings provide common regulatory mechanisms for endocrine control of animal development. (Tokushima University Institutional Repository) ● Metadata: 2009327 (Link to Publication Site) ● Publication site (DOI): 10.1073/pnas.1600612113 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 27140602 ● Summary page in Scopus @ Elsevier: 2-s2.0-84969765307 (Tokushima University Institutional Repository: 2009327, DOI: 10.1073/pnas.1600612113, PubMed: 27140602, Elsevier: Scopus)
15.	Hiroko Awata, Takahito Watanabe, Yoshitaka Hamanaka, Taro Mito, Sumihare Noji and Makoto Mizunami : Knockout crickets for the study of learning and memory: Dopamine receptor Dop1 mediates aversive but not appetitive reinforcement in crickets, Scientific Reports, 5, 15885, 2015. (Summary) Elucidation of reinforcement mechanisms in associative learning is an important subject in neuroscience. In mammals, dopamine neurons are thought to play critical roles in mediating both appetitive and aversive reinforcement. Our pharmacological studies suggested that octopamine and dopamine neurons mediate reward and punishment, respectively, in crickets, but recent studies in fruit-flies concluded that dopamine neurons mediates both reward and punishment, via the type 1 dopamine receptor Dop1. To resolve the discrepancy between studies in different insect species, we produced Dop1 knockout crickets using the CRISPR/Cas9 system and found that they are defective in aversive learning with sodium chloride punishment but not appetitive learning with water or sucrose reward. The results suggest that dopamine and octopamine neurons mediate aversive and appetitive reinforcement, respectively, in crickets. We suggest unexpected diversity in neurotransmitters mediating appetitive reinforcement between crickets and fruit-flies, although the neurotransmitter mediating aversive reinforcement is conserved. This study demonstrates usefulness of the CRISPR/Cas9 system for producing knockout animals for the study of learning and memory. (Tokushima University Institutional Repository) ● Metadata: 2007898 (Link to Publication Site) ● Publication site (DOI): 10.1038/srep15885 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 26521965 ● Search Scopus @ Elsevier (PMID): 26521965 ● Search Scopus @ Elsevier (DOI): 10.1038/srep15885 (Tokushima University Institutional Repository: 2007898, DOI: 10.1038/srep15885, PubMed: 26521965)
16.	Yuji Matsuoka, Tetsuya Bando, Takahito Watanabe, Yoshiyasu Ishimaru, Sumihare Noji, Aleksandar Popadic and Taro Mito : Short germ insects utilize both the ancestral and derived mode of Polycomb group-mediated epigenetic silencing of Hox genes., Biology Open, 4, 6, 702-709, 2015. (Summary) In insect species that undergo long germ segmentation, such as Drosophila, all segments are specified simultaneously at the early blastoderm stage. As embryogenesis progresses, the expression boundaries of Hox genes are established by repression of gap genes, which is subsequently replaced by Polycomb group (PcG) silencing. At present, however, it is not known whether patterning occurs this way in a more ancestral (short germ) mode of embryogenesis, where segments are added gradually during posterior elongation. In this study, two members of the PcG family, Enhancer of zeste (E(z)) and Suppressor of zeste 12 (Su(z)12), were analyzed in the short germ cricket, Gryllus bimaculatus. Results suggest that although stepwise negative regulation by gap and PcG genes is present in anterior members of the Hox cluster, it does not account for regulation of two posterior Hox genes, abdominal-A (abd-A) and Abdominal-B (Abd-B). Instead, abd-A and Abd-B are predominantly regulated by PcG genes, which is the mode present in vertebrates. These findings suggest that an intriguing transition of the PcG-mediated silencing of Hox genes may have occurred during animal evolution. The ancestral bilaterian state may have resembled the current vertebrate mode of regulation, where PcG-mediated silencing of Hox genes occurs before their expression is initiated and is responsible for the establishment of individual expression domains. Then, during insect evolution, the repression by transcription factors may have been acquired in anterior Hox genes of short germ insects, while PcG silencing was maintained in posterior Hox genes. (Tokushima University Institutional Repository) ● Metadata: 2007674 (Link to Publication Site) ● Publication site (DOI): 10.1242/bio.201411064 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 25948756 ● Search Scopus @ Elsevier (PMID): 25948756 ● Search Scopus @ Elsevier (DOI): 10.1242/bio.201411064 (Tokushima University Institutional Repository: 2007674, DOI: 10.1242/bio.201411064, PubMed: 25948756)
17.	Takahito Watanabe, Sumihare Noji and Taro Mito : Gene knockout by targeted mutagenesis in a hemimetabolous insect, the two-spotted cricket Gryllus bimaculatus, using TALENs., Methods, 69, 1, 17-21, 2014. (Summary) Hemimetabolous, or incompletely metamorphosing, insects are phylogenetically basal. These insects include many deleterious species. The cricket, Gryllus bimaculatus, is an emerging model for hemimetabolous insects, based on the success of RNA interference (RNAi)-based gene-functional analyses and transgenic technology. Taking advantage of genome-editing technologies in this species would greatly promote functional genomics studies. Genome editing using transcription activator-like effector nucleases (TALENs) has proven to be an effective method for site-specific genome manipulation in various species. TALENs are artificial nucleases that are capable of inducing DNA double-strand breaks into specified target sequences. Here, we describe a protocol for TALEN-based gene knockout in G. bimaculatus, including a mutant selection scheme via mutation detection assays, for generating homozygous knockout organisms. (Keyword) Animals / Deoxyribonucleases / Gene Knockout Techniques / Gryllidae / Homozygote / Mutagenesis, Site-Directed (Link to Publication Site) ● Publication site (DOI): 10.1016/j.ymeth.2014.05.006 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 24874787 ● Summary page in Scopus @ Elsevier: 2-s2.0-84929509568 (DOI: 10.1016/j.ymeth.2014.05.006, PubMed: 24874787, Elsevier: Scopus)

Review, Commentary:

1.	Taro Mito, Yoshiyasu Ishimaru, Takahito Watanabe, Taro Nakamura, Guillem Ylla, Sumihare Noji and G Cassandra Extavour : Cricket: The third domesticated insect., Current Topics in Developmental Biology, 147, 291-306, Mar. 2022. (Summary) Many researchers are using crickets to conduct research on various topics related to development and regeneration in addition to brain function, behavior, and biological clocks, using advanced functional and perturbational technologies such as genome editing. Recently, crickets have also been attracting attention as a food source for the next generation of humans. In addition, crickets are increasingly being used as disease models and biological factories for pharmaceuticals. Cricket research has thus evolved over the last century from use primarily in highly important basic research, to use in a variety of applications and practical uses. These insects are now a state-of-the-art model animal that can be obtained and maintained in large quantities at low cost. We therefore suggest that crickets are useful as a third domesticated insect for scientific research, after honeybees and silkworms, contributing to the achievement of global sustainable development goals. (Keyword) Animals / Bees / Gryllidae / Insecta (Link to Publication Site) ● Publication site (DOI): 10.1016/bs.ctdb.2022.02.003 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 35337452 ● Search Scopus @ Elsevier (PMID): 35337452 ● Search Scopus @ Elsevier (DOI): 10.1016/bs.ctdb.2022.02.003 (DOI: 10.1016/bs.ctdb.2022.02.003, PubMed: 35337452)
2.	Taro Mito, Takahito Watanabe and 岡部慎司 : 持続可能な次世代タンパク質源としての食用コオロギ, Seibutsu-kogaku Kaishi, 98, 1, 44-45, Jan. 2020.

Proceeding of International Conference:

1.	Shintaro Inoue, Takahito Watanabe, FUJIE Kai, SHIMAMURA Ayane, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Akira Takahashi, Takeshi Nikawa and Taro Mito : Melanin pigmentation is regulated via dopamine competition with the sclerotin biosynthesis pathway in the cuticle of hemimetabolous insects, The XXVII International Congress of Entomology 2024, Kyoto, Japan, Aug. 2024.
2.	Takeshi Nikawa, Katsuyuki Miyawaki, Akira Takahashi, Takahito Watanabe and Taro Mito : ANTI-MUSCLE ATROPHIC PROTEIN FOOD SOURCE IN SPACE: DEVELOPMENT OF A RECIRCULATORY REARING SYSTEM FOR SOYBEANS AND CRICKETS, 45th COSPAR Scientific Assembly-COSPAR 2024, Jul. 2024.
3.	Shintaro Inoue, Takahito Watanabe, Hamaguchi Taiki, Fujie Kai, Shimamura Ayane, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Takeshi Nikawa, Akira Takahashi, Sumihare Noji and Taro Mito : Artificial modification of cricket body color: breeding for the next-generation of protein supply, International Conference of Non-Traditional Arthropod Model Systems, Aug. 2023.
4.	Fujie Kai, Shintaro Inoue, Hamaguchi Taiki, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Takeshi Nikawa, Akira Takahashi, Sumihare Noji, Takahito Watanabe and Taro Mito : The discovery of two paralogous dopamine-synthase genes in the two-spotted cricket Gryllus bimaculatus, International Conference of Non-Traditional Arthropod Model Systems, Aug. 2023.
5.	Yuriko Osakabe, Kira Nozomu, Ueta Risa, Sakamoto Hideki, Takahito Watanabe, Takayanagi Eiko, Hara Chihiro, Hashimoto Ryosuke, Kohji Yamada and Keishi Osakabe : Development of in planta-regeneration system for plant genome editing, Frontiers in Genome Engineering 2019, Kobe Convention Center, Nov. 25-27, 2019, Nov. 2019.
6.	Risa Ueta, Chihiro Abe, Ryosuke Ishihara, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : Site-directed mutagenesis of the tomato IAA9 gene by using the CRISPR/Cas9 system, Latest Advances in Plant Development and Environmental Response 2016, CSH - Asia Meetings, Nov. 2016.
7.	Yuriko Osakabe, Risa Ueta, Sigeo Sugano, Takahito Watanabe, Kazuo Shinozaki and Keishi Osakabe : Genetic Engineering of Abiotic Stress Response in Plants, 3rd Conference of Cereal Biotechnology and Breeding, Nov. 2015.
8.	Matsuoka Yuji, Takahito Watanabe, Sayuri Tomonari, Sumihare Noji and Taro Mito : Functional analysis of a Hox gene, abdominal-A, using CRISPR/Cas9 system in the cricket Gryllus bimaculatus, International Tribolium Meeting 2015, Berkeley, USA, Aug. 2015.
9.	Takahito Watanabe, Matsuoka Yuji, Sayuri Tomonari, Kurita Chinami, Sumihare Noji and Taro Mito : Genome editing in the two-spotted cricket, Gryllus bimaculatus, using CRISPR/Cas9 system, Insect Genetic Technologies Workshop, Manhattan, Kansas, USA, Jun. 2015.
10.	Taro Mito, Itoh Takehiko, Morimoto Hiroya, Kajitani Ray, Toyoda Atsushi, Sayuri Tomonari, Fuketa Masao, Takahito Watanabe, Matsuoka Yuji and Sumihare Noji : Genome sequencing and annotation of the cricket Gryllus bimaculatus, a hemimetabolous insect model, Ninth Annual Arthropod Genomics Symposium, Manhattan, Kansas, USA, Jun. 2015.
11.	Sumihare Noji, Taro Mito, Bando Tetsuya, Nakamura Taro, Takahito Watanabe, Ishimaru Yoshiyasu and Hideyo Ohuchi : Regeneration of insect legs from stem cells, Thirteenth International Congress on Invertebrate Reproduction and Development, Detroit, Detroit, MI, USA, Jul. 2014.
12.	Takahito Watanabe, Sumihare Noji and Taro Mito : Targeted genome modifications in the cricket, Gryllus bimaculatus, using CRISPR/Cas9 system, International Symposium on RNAi and Genome editing methods, Tokushima, Japan, Mar. 2014.
13.	Taro Mito, Takahito Watanabe and Sumihare Noji : Genome modification technology in the cricket Gryllus bimaculatus, 1st Asian Invertebrate Immunity Symposium, Busan, Feb. 2014.
14.	Takahito Watanabe, Matsuoka Yuji, Sumihare Noji and Taro Mito : Targeted genome editing in the cricket, Gryllus bimaculatus, using CRISPR/Cas9 system, FASEB SRC on Genome Engineering-Cutting-Edge Research and Applications, Nassau, Bahamas, Jan. 2014.
15.	Takahito Watanabe, Ochiai Hiroshi, Sakuma Tetsushi, Ishihara Satoshi, Nakamura Taro, Yamamoto Takashi, Sumihare Noji and Taro Mito : Targeted genome modifications in the cricket, Gryllus bimaculatus, Conference of Transposition & Genome Engineering 2013, Budapest, Hungary, Sep. 2013.

Proceeding of Domestic Conference:

1.	Shintaro Inoue, FUJIE Kai, HAMAGUCHI Taiki, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Akira Takahashi, Takeshi Nikawa, Sumihare Noji, Takahito Watanabe and Taro Mito : コオロギ科GryllidaeファミリーにおけるDOPA-decarboxylase遺伝子の系統特異的重複と機能多様化, 第69回日本応用動物昆虫学会大会, Mar. 2025.
2.	SHIMAMURA Ayane, Shintaro Inoue, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Akira Takahashi, Sumihare Noji, Takahito Watanabe and Taro Mito : フタホシコオロギの体色パターン形成における白色スクレロチン合成酵素遺伝子の発現と機能の解析, 第47回日本分子生物学会年会, Nov. 2024.
3.	NAKAMURA Minami, HIROKI Matsuki, HAGIWARA Kanon, Shoichiro Takao, Katsuyuki Miyawaki, Takahito Watanabe, 片岡孝介, 蘆刈晟也, Akira Takahashi, Takayuki Uchida and Takeshi Nikawa : コオロギ摂食による栄養学的な機能性検討, 第57回日本栄養・食糧学会中国・四国支部大会, Nov. 2024.
4.	NAKAMURA Minami, HIROKI Matsuki, ANAYT ULLA, Takayuki Uchida, Kazuaki Mawatari, Akira Takahashi, Shoichiro Takao, Katsuyuki Miyawaki, Takahito Watanabe, Taro Mito, Takayoshi Kuriki, 片岡孝介, 葦苅晟矢 and Takeshi Nikawa : コオロギ摂食による栄養学的な機能性検討, 第78回日本栄養・食糧学会大会, May 2024.
5.	岸伸旺, Takahito Watanabe, Shintaro Inoue, 濱口汰暉, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Akira Takahashi, Takeshi Nikawa, Sumihare Noji and Taro Mito : フタホシコオロギにおけるクチクラ色素合成に関わる遺伝子の機能解析, 第68回応用動物昆虫学会, -, -, -, Mar. 2024.
6.	Shintaro Inoue, Takahito Watanabe, 藤江快, 島村彩音, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Akira Takahashi, Takeshi Nikawa and Taro Mito : コオロギをモデルとした昆虫の白色スクレロチン合成酵素遺伝子のメラニン生成制御機能の解析, 第68回応用動物昆虫学会, -, -, -, Mar. 2024.
7.	Takahito Watanabe : 循環型タンパク質としてのコオロギについて, フードテック啓発セミナー, -, -, -, Feb. 2024.
8.	NAMIKAWA Sayaka, Yoshiyasu Ishimaru, Sayuri Tomonari, Takahito Watanabe, Sumihare Noji and Taro Mito : フタホシコオロギにおける20-hydroxyecdysone(20E)合成に関わるBlimp-1遺伝子の機能解析, 第46回日本分子生物学会, Dec. 2023.
9.	Takahito Watanabe : サステナブルで美味しい食の選択肢としての食用コオロギ, 全国高等学校長協会, -, -, -, Nov. 2023.
10.	Takahito Watanabe : 循環型タンパク質としての食用コオロギについて, 第53回中国四国大学保健管理研究集会, -, -, -, Aug. 2023.
11.	Takahito Watanabe : 循環型タンパク質としての食用コオロギについて, 第56回全国手話通訳問題研究集会サマーフォーラム in とくしま, -, -, -, Aug. 2023.
12.	Takahito Watanabe : 循環型食品としての食用コオロギについて, 生物工学会シンポジウム, -, -, -, Jul. 2023.
13.	HIROKI Matsuki, MINORI Suzuki, KONO Madoka, ANAYT ULLA, Kazuaki Mawatari, Akira Takahashi, Katsuyuki Miyawaki, Takahito Watanabe, Taro Mito, Takayoshi Kuriki and Takeshi Nikawa : コオロギの抗筋萎縮作用について, 第77回日本栄養・食糧学会大会, May 2023.
14.	Takahito Watanabe : 循環型食品としての食用コオロギについて, ifiaJAPAN2023, -, -, -, May 2023.
15.	Takahito Watanabe : 食用コオロギの社会実装とゲノム編集による品種改良について, 中国四国地区生物系三学会合同大会, -, -, -, May 2023.
16.	Takahito Watanabe : 循環型タンパク質としての食用コオロギについて, 農学会公開シンポジウム, -, -, -, Apr. 2023.
17.	Takahito Watanabe : コオロギに関する基礎研究と，食用コオロギという社会実装について, 科学技術と経済の会シンポジウム, Mar. 2023.
18.	Takahito Watanabe : コオロギ研究の可能性 ~大学での基礎研究から起業による社会実装まで~, ⽇本動物学会関東⽀部⼤会公開シンポジウム, Mar. 2023.
19.	Takahito Watanabe : 食用コオロギビジネスの最前線, 第三回JATAFF安全性・品質保証部会, Mar. 2023.
20.	Shintaro Inoue, Takahito Watanabe, Taiki HAMAGUCHI, Yoshiyasu Ishimaru, Katsuyuki Miyawaki, Takeshi Nikawa, Akira Takahashi, Sumihare Noji and Taro Mito : コオロギをモデルとした体色パターン制御の分子メカニズムの解析, 第67回日本応用動物昆虫学会, Mar. 2023.
21.	Takahito Watanabe : コオロギ食用化に向けた取り組み ~大学での研究から起業による社会実装まで~, 第67回日本応用動物昆虫学会, Mar. 2023.
22.	Takahito Watanabe : コオロギが実現する持続可能な食用タンパク質生産, 日本学術会議事例紹介, Mar. 2023.
23.	Takahito Watanabe : 新規食品昆虫食の現状と課題, 第18回食品安全シンポジウム, Mar. 2023.
24.	Takahito Watanabe : なぜコオロギ? ~昆虫食からSDG'sを考える~, 尼崎市主催市民公開講座, Dec. 2022.
25.	Taiki HAMAGUCHI, Shintaro Inoue, Katsuyuki Miyawaki, Akira Takahashi, Takeshi Nikawa, Yoshiyasu Ishimaru, Sumihare Noji, Takahito Watanabe and Taro Mito : フタホシコオロギにおける色素合成に関わる遺伝子の機能解析, 第45回日本分子生物学会, Dec. 2022.
26.	平田愛佳, 佐藤匠, 増田尚輝, Chenjuan Yao, Rie Mukai, Takahito Watanabe, Taro Mito and Tetsuya Akamatsu : コオロギ食が唾液腺機能に及ぼす効果の検証, 第1回唾液ケア研究会学術集会, Nov. 2022.
27.	Takahito Watanabe : 食用コオロギの事業内容と研究者の起業について, 化学とマイクロ・ナノシステム学会第46回研究会, Nov. 2022.
28.	Takahito Watanabe : 食用コオロギ研究による地域・社会への貢献, 富岡西高校, Oct. 2022.
29.	Takahito Watanabe : 持続可能な循環型タンパク質としてのコオロギの可能性, ニューシルクロード協議会, Oct. 2022.
30.	Takahito Watanabe : 持続可能な循環型タンパク質としてのコオロギの可能性, 第12回CSJ化学フェスタ2022, Oct. 2022.
31.	Takahito Watanabe : 循環型タンパク質としての食用コオロギの可能性, 徳島ロータリークラブ定例会講演, Sep. 2022.
32.	平田愛佳, 佐藤匠, 田中寛人, 増田尚輝, Chenjuan Yao, Rie Mukai, Takahiro Hasegawa, Hiroshi Yoshimura, Takahito Watanabe, Taro Mito and Tetsuya Akamatsu : 食品成分が唾液腺機能に及ぼす影響, 第34回唾液腺談話会, Sep. 2022.
33.	Takahito Watanabe, Shintaro Inoue, Taiki HAMAGUCHI, Yoshiyasu Ishimaru and Taro Mito : ゲノム編集を活用した食用コオロギの育種研究, 日本遺伝学会第94回大会, Sep. 2022.
34.	Takahito Watanabe : 循環型タンパク質としての食用コオロギの可能性, 第23回日本食品工学会, Sep. 2022.
35.	Takahito Watanabe : 循環型食品としての食用コオロギの可能性, Daiwa Innovation Network, Aug. 2022.
36.	Takahito Watanabe : 徳島大学の取り組み, アイ・エフ・キューブプロジェクトシンポジム∼地球規模の食料問題の解決と人類の宇宙進出に向けた昆虫が支える循環型食料生産システムの開発∼, Aug. 2022.
37.	Takahito Watanabe : 循環型食品としての食用コオロギの可能性, 広島バイオフォーラム, Jul. 2022.
38.	HIROKI Matsuki, Minori Yamasaki, KONO Madoka, NAKANO Wataru, (名) ANAYTULLA, Akira Takahashi, Katsuyuki Miyawaki, Takahito Watanabe, Taro Mito, Takayoshi Kuriki and Takeshi Nikawa : コオロギの抗筋萎縮作用について, 第76回日本栄養・食糧学会大会, Jun. 2022.
39.	Takahito Watanabe : グリラスの事業内容と私が起業した理由, 第56回日本発生生物学会キャリアパスセミナー, Jun. 2022.
40.	Takahito Watanabe : コオロギ × テクノロジーが生み出す新たな調和で実現する健康でしあわせな未来, LIFE Universityセミナー, Apr. 2022.
41.	Takahito Watanabe : コオロギ × テクノロジーが生み出す新たな調和で実現する健康でしあわせな未来, フードテックオンラインセミナー, Apr. 2022.
42.	Takahito Watanabe : 昆虫食を「サーキュラーフード」にアップデートするという挑戦, WIREDオンライン「THURS DAY NIGHT」, Apr. 2022.
43.	Shintaro Inoue, HAMAGUCHI Taiki, Yoshiyasu Ishimaru, Taro Mito and Takahito Watanabe : フタホシコオロギの体色関連遺伝子のノックアウト系統作製および表現型解析, 第66回日本応用動物昆虫学会大会, Mar. 2022.
44.	Naoki Masuda, Takaiku Sakamoto, 西海信, Takahito Watanabe, Eiji Sakuradani, Taro Mito and Rie Mukai : 食用昆虫の摂取が実験動物の代謝に及ぼす影響, 日本農芸化学会2022年度大会, Mar. 2022.
45.	Takahito Watanabe : 食品ロスを循環させる新たなタンパク源としての「食用コオロギ」, 健康博覧会2022, Feb. 2022.
46.	MASUDA Naoki, Takaiku Sakamoto, 西海信, Takahito Watanabe, Eiji Sakuradani, Taro Mito and Rie Mukai : 食用昆虫の脂質組成分析と実験動物への影響, 2021年度第3回脂質駆動学術産業創生研究部会講演会, Dec. 2021.
47.	Hamaguchi Taiki, Shintaro Inoue, Takahito Watanabe, Yoshiyasu Ishimaru and Taro Mito : フタホシコオロギにおけるクチクラ形成と色素合成に関わる遺伝子の機能解析, The 44th Annual Meeting of the Molecular Biology Society of Japan, Dec. 2021.
48.	Takahito Watanabe : 世界のタンパク質不足と食品ロス問題を解消する循環型タンパク質「食用コオロギ」の生産・販売, アグリビジネス創出フェア2021, Nov. 2021.
49.	Takahito Watanabe : 食品ロスを解決する循環型``サーキューラーフード''と原料の開発状況について, 第1回国際食品商談Week, Nov. 2021.
50.	Takahito Watanabe : 循環型食材``サーキュラーフード''としての食用コオロギの可能性について, 食品開発展2021, Oct. 2021.
51.	Takahito Watanabe : 昆虫から地球の未来をどう学ぶ?, SHIBUYA QWS主催パネルディスカッション, Apr. 2021.
52.	Takahito Watanabe : 新食品資源としての循環型食用コオロギタンパク開発の現状と応用, 日本産業機械工業会環境ビジネス委員会, Dec. 2020.
53.	Takahito Watanabe : 徳島大学おける研究内容と(株)グリラスの活動内容, ムーンショット型農林水産研究開発事業「地球規模の食料問題の解決と人類の宇宙進出に向けた昆虫が支える循環型食料生産システムの開発」キックオフシンポジウム, Dec. 2020.
54.	Takahito Watanabe : コオロギを食料資源に! ∼循環型タンパク質生産体制構築の試み∼, 徳島大学公開シンポジウム「SDGsの達成に向けて」, Nov. 2020.
55.	Takahito Watanabe : 新食品資源としての循環型食用コオロギタンパク開発の現状と応用, 食品開発展2020, Nov. 2020.
56.	Takahito Watanabe : Gryllusの未来に向けた挑戦, ヨコハマ・パラトリエンナーレ, Oct. 2020.
57.	山下貴久, 大出高弘, Sayuri Tomonari, 中村雄軌, Yoshiyasu Ishimaru, Takahito Watanabe and Taro Mito : フタホシコオロギの翅形成に関わる遺伝子の発現と機能解析, 第91回日本動物学会, Sep. 2020.
58.	Sumihare Noji, Takahito Watanabe, Yoshiyasu Ishimaru, Taro Mito and 岡部慎司 : コオロギ(昆虫)を用いた宇宙食, 第63回宇宙科学技術連合講演会, Nov. 2019.
59.	吉良望, 高柳栄子, Takahito Watanabe, 坂本秀樹, Chihiro Hara, Ryosuke Hashimoto, Risa Ueta, Yuriko Osakabe, Yuriko Osakabe and Keishi Osakabe : トマトゲノム編集のためのin planta-regeneration法の開発, 第37回日本植物細胞分子生物学会大会,京都府立大学, 2019年9月7日-8日, Sep. 2019.
60.	吉良望, 高柳栄子, Takahito Watanabe, Risa Ueta, Takahito Watanabe, Chihiro Hara, Ryosuke Hashimoto, Yuriko Osakabe and Keishi Osakabe : トマトゲノム編集のためのin planta-regeneration法の開発, 日本ゲノム編集学会第4回大会, タワーホール船堀(東京), 2019年6月4日-5日, Jun. 2019.
61.	Kohei Kawamoto, Mayuko Matsuda, Takahisa Yamashita, Takahito Watanabe, Sayuri Tomonari, Yoshiyasu Ishimaru, Sumihare Noji and Taro Mito : Precise in-frame integration of a GFP gene using microhomology-mediated knock-in technology in Gryllus bimaculatus, 52nd Annual Meeting of the Japanese Society of Developmental Biologists, May 2019.
62.	Takahisa Yamashita, Taro Mito, Yoshiyasu Ishimaru, Takahito Watanabe, Sayuri Tomonari, Kohei Kawamoto and Mayuko Matuda : Generation of an enhancer-trap strain of the scalloped gene in the cricket Gryllus bimaculatus, 52nd Annual Meeting of the Japanese Society of Developmental Biologists, May 2019.
63.	Yuki Nakamura, Sayuri Tomonari, Kohei Kawamoto, Takahito Watanabe, Yoshiyasu Ishimaru, Sumihare Noji and Taro Mito : Resolving the correlation between phenotype and genotype in a segmentation gene even-skipped in the cricket Gryllus bimaculatus, 52nd Annual Meeting of the Japanese Society of Developmental Biologists, May 2019.
64.	吉良望, Risa Ueta, Takahito Watanabe, 高柳栄子, 坂本秀樹, Chihiro Abe, Ryosuke Hashimoto, Yuriko Osakabe and Keishi Osakabe : Development of in planta-regeneration system for genome editing in tomato, 第60回日本植物生理学会年会, 名古屋大学, 2019年3月13日-15日, Mar. 2019.
65.	吉良望, 高柳栄子, 坂本秀樹, Takahito Watanabe, Chihiro Abe, Ryosuke Hashimoto, Yuriko Osakabe and Keishi Osakabe : トマト茎頂組織への新規in planta 遺伝子導入法の開発, 第36回日本植物分子生物学会(金沢)大会, 金沢商工会議所会館, 2018年8月26∼28日, Aug. 2018.
66.	吉良望, 高柳栄子, 坂本秀樹, Takahito Watanabe, Chihiro Abe, Ryosuke Hashimoto, Yuriko Osakabe and Keishi Osakabe : トマト茎頂組織への新規in planta 遺伝子導入法の開発, 日本ゲノム編集学会第3回大会, 広島国際会議場(広島市), 2018年6月16日-20日, Jun. 2018.
67.	Yu-ki Nakamura, Ko-hei Kawamoto, Sayuri Tomonari, Takahito Watanabe, Yoshiyasu Ishimaru, Taro Mito and Sumihare Noji : Gene knock-out analysis of a segmentation gene even-skipped in the cricket Gryllus bimaculatus, Joint Annual Meeting of JSDB 51st and JSCB 70th, Jun. 2018.
68.	吉良望, 高柳栄子, 坂本秀樹, Takahito Watanabe, 阿部千尋, 橋本諒典, Yuriko Osakabe and Keishi Osakabe : In planta genome editing in tomato meristem tissues, 第59回日本植物生理学会年会, Mar. 2018.
69.	上村菜月, Sayuri Tomonari, Takahito Watanabe, 松岡佑児, Yoshiyasu Ishimaru, Sumihare Noji and Taro Mito : 遺伝子ノックイン技術の応用によるレポーターコオロギ系統の作製, 第88回日本動物学会, Sep. 2017.
70.	上田梨紗, 阿部千尋, 橋本諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : トマトの機能改変を目指した高効率ゲノム編集技術の確立, 日本ゲノム編集学会第2回大会, 千里ライフサイエンスセンター, 大阪, Jun. 2017.
71.	Matsuda Mayuko, Matsuoka Yuji, Yoshiyasu Ishimaru, Sayuri Tomonari, Takahito Watanabe, Sumihare Noji and Taro Mito : Functional analysis of a Hox gene, abdominal-A, in the cricket Gryllus bimaculatus using a CRISPR/Cas9-mediated gene knock-in system, Japanese Society of Developmental Biologists, May 2017.
72.	Nakamura Yu-Ki, Kawamoto Kohei, Sayuri Tomonari, Matsuda Mayuko, Takahito Watanabe, Yoshiyasu Ishimaru, Uemura Natsuki, Sumihare Noji and Taro Mito : even-skipped is required for segmentation and elongation of embryos in the cricket Gryllus bimaculatusas revealed by CRISPR/Cas9-based gene knock-out., Japanese Society of Developmental Biologists, May 2017.
73.	Masamitsu Takai, Takahito Watanabe, Sayuri Tomonari and Taro Mito : フタホシコオロギの食用化に向けた生産システムの検討, 第61回日本応用動物昆虫学会大会, Mar. 2017.
74.	阿部千尋, 上田梨紗, 橋本諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : 栽培品種トマトAilsa Craigの CRISPR/Cas9システムを用いた新育種技術開発, 第58回日本植物生理学会年会, Mar. 2017.
75.	Risa Ueta, Chihiro Abe, Ryosuke Ishihara, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : Rapid breeding of parthenocarpic tomato plants using CRISPR/Cas9, 第58回日本植物生理学会年会, Mar. 2017.
76.	阿部千尋, 上田梨紗, 橋本諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : 栽培品種トマトAilsa Craigの CRISPR/Cas9システムを用いた新育種技術開発, 日本生物工学会西日本支部第3回講演会, Dec. 2016.
77.	上田梨紗, 阿部千尋, 橋本諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : CRISPR/Cas9によるトマトIAA9遺伝子を標的としたゲノム編集技術の確立, 第3回日本生物工学会西日本支部講演会, Dec. 2016.
78.	坂本秀樹, Takahito Watanabe, 上田梨紗, 島田佳南里, 福原真樹, Yuriko Osakabe and Keishi Osakabe : 電気穿孔を用いた直接導入法およびin planta法による植物ゲノム編集技術の開発, 第39回日本分子生物学会年会, Nov. 2016.
79.	上田梨紗, 阿部千尋, 石原諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : CRISPR/Cas9によるトマトIAA9遺伝子を標的としたゲノム編集技術の確立, 日本植物学会第80回大会, Sep. 2016.
80.	Yuriko Osakabe, Takahito Watanabe, Sigeo Sugano, 上田梨紗, 石原諒典, 篠崎一雄 and Keishi Osakabe : ゲノム編集技術による植物環境応答能の改変, 日本ゲノム編集学会第1回大会, Sep. 2016.
81.	阿部千尋, 上田梨紗, 石原諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : 栽培品種トマトAilsa Craigの CRISPR/Cas9システムを用いた新育種技術開発, 日本ゲノム編集学会第1回大会, Sep. 2016.
82.	上田梨紗, 阿部千尋, 石原諒典, Takahito Watanabe, Sigeo Sugano, Yuriko Osakabe and Keishi Osakabe : CRISPR/Cas9によるトマトIAA9遺伝子を標的としたゲノム編集技術の確立, 日本ゲノム編集学会第1回大会, Sep. 2016.
83.	Kohei Kawamoto, Sayuri Tomonari, Yuji Matsuoka, Takahito Watanabe, Yoshiyasu Ishimaru, Sumihare Noji and Taro Mito : even-skipped acts principally as a gap gene in the cricket Gryllus bimaculatus as revealed by CRISPR/Cas9-based gene knockout analysis, JSDB Special Symposium: Frontier of Developmental Biology Hosted by JSDB, Jun. 2016.
84.	上田梨紗, 阿部千尋, 石原諒典, Takahito Watanabe, Sigeo Sugano, Katsuyuki Miyawaki, Sumihare Noji, Yuriko Osakabe and Keishi Osakabe : 高効率 CRISPR/Cas9による SlIAA9 ノックアウトトマトの作出, 第57回日本植物生理学会大会, Mar. 2016.
85.	Yuriko Osakabe, Sigeo Sugano, Takahito Watanabe, 上田梨紗, 石原諒典, 篠崎一雄 and Keishi Osakabe : CRISPR/Cas9によるシロイヌナズナ環境ストレス応答性遺伝子のゲノム編集, 第57回日本植物生理学会大会, Mar. 2016.
86.	上田梨紗, 石原諒典, 阿部千尋, Takahito Watanabe, Sigeo Sugano, Katsuyuki Miyawaki, Sumihare Noji, Yuriko Osakabe and Keishi Osakabe : CRISPR/Cas9によるトマトIAA9 遺伝子を標的としたゲノム編集技術の確立, 第38回日本分子生物学会年会, Dec. 2015.
87.	Sayuri Tomonari, 川本晃平, 松岡佑児, Takahito Watanabe, Yoshiyasu Ishimaru, Sumihare Noji and Taro Mito : CRISPR/Cas9システムを用いた遺伝子ノックアウトによるコオロギ胚発生制御メカニズムの解析, 第38回日本分子生物学会年会, Dec. 2015.
88.	Yuji Matsuoka, Takahito Watanabe, 栗田千波, Sayuri Tomonari, Sumihare Noji and Taro Mito : フタホシコオロギにおけるCRISPR/Cas9システムを用いたHox遺伝子abdominal-Aの機能解析, 第48回日本発生生物学会, Jun. 2015.
89.	上田梨紗, 石原諒典, Takahito Watanabe, 菅野茂夫, 宮脇克行, 野地澄晴, Yuriko Osakabe and Keishi Osakabe : CRISPR/Cas9によるトマトIAA9遺伝子を標的としたゲノム編集技術の確立, 第56回日本植物生理学会年会, Mar. 2015.
90.	Yuji Matsuoka, Tetsuya Bando, Takahito Watanabe, Sumihare Noji and Taro Mito : Functions of Polycomb group gene in regulation of Hox gene expression in a primitive mode of insect embryogenesis in the cricket Gryllus bimaculatus, 第47回日本発生生物学会, May 2014.
91.	Takahito Watanabe, Yuji Matsuoka, Taro Mito and Sumihare Noji : Targeted gene disruption in the cricket, Gryllus bimaculatus, using CRISPR/Cas9 system, 第47回日本発生生物学会, May 2014.
92.	平田翔悟, 上田梨紗, Takahito Watanabe, Katsuyuki Miyawaki, 三戸太郎 and 野地澄晴 : Transcription Activator-Like Effector NucleasesによるIAA9ノックアウトトマト作製の試み, 第36回日本分子生物学会, Dec. 2013.

Et cetera, Workshop:

1.	Takahito Watanabe : 昆虫工場研究開発の現状と植物工場との統合の可能性, 植物工場研究会, -, -, -, Apr. 2023.
2.	Takahito Watanabe : サーキュラーフードという新常識 ~コオロギは地球を救う~, 東京エレクトロン社内講演, Sep. 2022.
3.	Takahito Watanabe : 持続可能な循環型タンパク質としての食用コオロギ, 第66回バイオ・マイクロ・ナノテク研究会, Mar. 2022.
4.	Takahito Watanabe : サーキュラーフードとしての食用コオロギビジネスの事業展開について, 食品ニューテクノロジー研究会, Mar. 2022.
5.	Takahito Watanabe : 循環型食品``サーキュラーフード''としての食用コオロギについて, フード・フォラム・つくば, Dec. 2021.
6.	Takahito Watanabe : 革新的なアグリ・フードテックサービスのスケールに向けた成長戦略, AG/SUM Symposium 2021パネルディスカッション, Jun. 2021.
7.	Takahito Watanabe : 新たな循環型タンパク質としての食用コオロギ生産∼基礎研究から応用研究，そして会社経営へ∼, 第20回シカゴ在住若手研究者による研究会, Apr. 2021.
8.	Takahito Watanabe : 徳島大学発ベンチャーと無印良品の商品開発 ∼コオロギがせんべいに?∼, 「『食』を通じた新たな産学創造に学ぶ∼産学の知恵∼」オンラインセミナー, Aug. 2020.
9.	Aya Nakai, koji Murai, Akihito Tanaka, Hiroshi Kondoh, Sugina Watanabe, Akiko Uebansou, Takahito Watanabe and Katsuyuki Miyawaki : LED植物工場を活用した藍の生育と二次代謝物質生産の制御, LED総合フォーラム2019 in徳島, 63-64, Feb. 2019.
10.	Akihiro Yasue, Silvia Naomi Mitsui Akagi, Takahito Watanabe, 佐久間哲史, Seiichi Oyadomari, 山本卓, Sumihare Noji, Taro Mito and Eiji Tanaka : TALEN，CRISPR/Casシステムを用いたマウス1細胞期胚における標的遺伝子破壊, 第3回ゲノム編集研究会, Oct. 2013.

Patent:

1.	Takahito Watanabe, Taro Mito, 三浦望, 河合重和, 村田康弘 and 高里明洋 : 飼育装置, 2020-195732 (Nov. 2020), .
2.	Takahito Watanabe, Taro Mito, 村田康弘, 高里明洋, 河合重和 and 三浦望 : 飼育装置, 2020-195731 (Nov. 2020), .
3.	Takahito Watanabe, Taro Mito, 村田康弘, 高里明洋 and 河合重和 : 飼育装置, 2020-172186 (Oct. 2020), .
4.	Takahito Watanabe, Taro Mito, 村田康弘, 高里明洋 and 河合重和 : 飼育装置, 2020-172185 (Oct. 2020), .
5.	Takahito Watanabe, Taro Mito, 河合重和, 村田康弘 and 松本崇 : 飼育装置, 2020-52445 (Mar. 2020), .
6.	Takahito Watanabe and Taro Mito : コオロギの育成装置及び育成方法, 2020-019352 (Feb. 2020), .
7.	Taro Mito and Takahito Watanabe : 遺伝子改変不完全変態昆虫の作製方法, 2017-196367 (Oct. 2017), 2019-068762 (May 2019), JP2019-068762A (May 2019).

Grants-in-Aid for Scientific Research (KAKEN Grants Database @ NII.ac.jp)

Analysis of mechanisms of regeneration-bud formation in the cricket using novel genetic engineering method (Project/Area Number: 16K21199 )
Analysis of mechanisms of wing development in hemimetabolous insect using conditional knock-out method. (Project/Area Number: 26870415 )
Study on genomic basis of morphogenesis in hemimetabolous insects using novel genetic modification techniques (Project/Area Number: 26292176 )
Search by Researcher Number (30709481)

Associate Professor : Watanabe, Takahito

Research

Personal Web Page

Field of Study

Subject of Study

Book / Paper

Book:

Academic Paper (Judged Full Paper):

Review, Commentary:

Proceeding of International Conference:

Proceeding of Domestic Conference:

Et cetera, Workshop:

Patent:

Grants-in-Aid for Scientific Research (KAKEN Grants Database @ NII.ac.jp)