Cover Page Gallery

  • 2025 Vol.42 No.1
    Double-immunostaining of actin filaments and microtubules

    The cover photograph shows a root cell of Arabidopsis thaliana that was simultaneously immunostained with anti-actin and anti-α-tubulin antibody. The images are as follows: left shows anti-actin staining, middle shows anti-α-tubulin staining, and right shows the merged image. This study presents a whole-mount immunostaining technique for the double labeling of actin filaments and microtubules.

    These photographs were taken by Toshiki Amari and Hirotomo Takatsuka in Kanazawa University, Japan, 2024 (Nikon A1 confocal laser scanning microscope system equipped with CFI SR HP Plan-Apochromat Lamda S 100xC silicon immersion objective). Adapted from Amari et al (pp. 87–92).

  • 2024 Vol.41 No.4
    Near-complete genome assembly of a miniature tomato cultivar Micro-Tom

    We present the genome assembly of a miniature tomato cultivar, Micro-Tom (Shirasawa & Ariizumi, pp. 367–374). As there are genetic variations in the Micro-Tom lines (Nagasaki et al. 2024, DNA Res 13: dsae016), the genome data of the standard line used in NBRP-Tomato, where massive genomic and genetic resources are developed, was required. We therefore launched the genome project on this line at JSOL2022 meeting (October 8–9, 2022, at Okayama University) and decided to present the result in the next meeting. We used a high-fidelity long-read sequencing technology and successfully completed the analysis within a year. The data was released through bioRxiv (October 31, 2023) and the achievement was announced at JSOL2023 (November 9–10, 2023, at Osaka Metropolitan University), thus fulfilling the promise. Subsequently, the genome data was honorably selected as the NCBI reference sequence of tomato due to the highest quality assembly reported to date.

    Illustration by Kenta Shirasawa (Kazusa DNA Research Institute) using Circos program.

  • 2024 Vol.41 No.3
    Synthetic biology and bioproduction in plants

    This cover illustrates the concept of synthetic biology and bioproduction in plants. Plants absorb CO2 and, through the introduction of gene circuits from other organisms or artificially generated, can produce a variety of products, including pharmaceuticals, fine chemicals, raw materials for bioplastics, biofuels, and more.
    The concepts of gene editing, metabolic pathway shifting, gene network manipulation, and the DBTL (Design-Build-Test-Learn) cycle are crucial for the implementation of synthetic biology and bioproduction in plants. The goal of synthetic biology and bioproduction in plants is to contribute to carbon recycling, which is a central component of the bioeconomy. Chemical structures of lignin, acteoside, menthol, corosolic acid, and isoprene are described clockwise from left top.

    Designed by Space Time Inc.

  • 2024 Vol.41 No.2
    Downregulation of a Phi class glutathione S-transferase gene in transgenic torenia yielded pale flower color

    The anthocyanin related glutathione S-transferase (GST) belongs to the Phi class of the GST family and has been regarded to play a role in anthocyanin transport to the vacuole. We isolated its orthologue from the torenia petal. Transgenic plants transcribing GST double stranded RNA were generated from a blue torenia. Resultant plants exhibited a range of flower colors, from blue to almost white. However, pure white flowers were not obtained in site of significant downregulation of the GST transcript. Anthocyanin levels in the petals of the transgenic plants decreased, whereas flavone levels remained unchanged. Anthocyanins and flavones may be transported to the vacuole through different mechanisms (Akagi et al, pp. 147–151) .

  • 2024 Vol.41 No.1
    Subcellular localization of AtGTLP in Arabidopsis root cells

    AtGTLP is a novel trans-Golgi-localized Arabidopsis protein with characteristics of a glycosyltransferase. The micrograph shows root cells after double visualization of Arabidopsis line co-expressing AtGTLP-mGFP and a mRFP-tagged trans-Golgi marker, ST. Subcellular localization was observed using Zeiss LSM980 confocal laser scanning microscope system equipped with Plan-Apochromat 63x/1.40 Oil DIC M27 immersion objective. Adapted from: Rzepecka et al. (pp. 35–44).

  • 2023 Vol.40 No.4
    Variety-dependent accumulation of glucomannan in the endosperm cell walls of rice grains

    Plant cell wall plays important roles in the regulation of plant growth/development and affects the quality of plant-derived foods. Genetic variability of cell wall components within a plant species, however, has not been well understood. In this issue, Zamorski et al. showed that the endosperm cell walls from 89 rice varieties were clearly classified into two groups, depending on the presence/absence of β-1,4-linked glucomannan (See Zamorski et al, pp. 321–336). Immunoelectron microscopic observation of developing rice grains with an anti-Man4 antibody often detected the accumulation of glucomannan (indicated by the presence of gold particles) in the middle portion of the thick aleurone cell walls of a glucomannan-positive variety, Fujisaka-5, suggesting that the glucomannan was synthesized in the early stage of endosperm development but the synthesis was downregulated during the secondary thickening process associated with the differentiation of aleurone layer.

  • 2023 Vol.40 No.3
    This special issue contains articles reporting on the latest advancements in genome editing technology and its application for the development of crop varieties and breeding materials.

    This cover shows photos of genome-edited under research and development in Japan.
    (Top left) Site-directed mutagenesis in two GmPPD genes in soybean (Glycine max). Photographed by Jaechol Sim using a smartphone camera (Galaxy S10 5G) at Hokkaido University (Sapporo, Japan).
    (Top right) Double-flowered gentian produced by genome editing of AG1 gene. Photographed by Masahiro Nishihara using a digital camera (Olympus E-M10) at Iwate Biotechnology Research Center (Iwate, Japan).
    (Bottom left) Field cultivation of genome-edited wheat. Photographed by Fumitaka Abe using a smartphone camera (SONY Xperia) at The National Agriculture and Food Research Organization (NARO) (Ibaraki, Japan).
    (Bottom right) Harvesting genome-edited potato tubers with reduced accumulation of steroidal glycoalkaloids grown in an open field. Photographed by Yuki Sasakawa using a digital camera (Lumix DMC-GX7) at NARO (Ibaraki, Japan).
    Designed by Shuhei Yasumoto.

  • 2023 Vol.40 No.2
    ntergeneric hybridization between marguerite (Argyranthemum frutescens) and Rhodanthemum catananche using ovule culture

    Intergeneric hybridization is an effective strategy for increasing variation and conferring useful traits to organisms. In this study, intergeneric hybrids of marguerite (Argyranthemum frutescens) and two Rhodanthemum species (R. hosmariense and R. catananche) were obtained via ovule culture (See Katsuoka et al., pp. 135–143). The two resulting hybrids exhibited blooming characteristics inherited from both parents. The leaf shape and other morphological traits of the progenies were intermediate between those of the parents. This study provides a basis for further development of Argyranthemum breeding, especially that of a series of hybrid cultivars with different flower colors.
    These photographs were taken using an iPhone 7 at the Izu Agricultural Research Center (Shizuoka, Japan) in March 2022.

  • 2023 Vol.40 No.1
    A developed system to extract specific responses of increment length in rice shoots under gradient changes in nitrogen concentration regimes

    Optimal media of Piriformospora indica to release effective VOC for plant growth. Utilization of beneficial microorganism will overcome food shortage issue by enhancing crop productivity as well as conserving environmental balance. The fungus Piriformospora indica is a beneficial root-colonizing microorganism that can promote plant resistance and growth by producing diffusible and/or volatile organic compounds (VOCs). The cover photography shows that P. indica grown on different media releases different VOCs by altering the metabolism and induces differential effects on plant growth. (See Bayubaskara et al, pp. 117–121)
    This photograph was taken by Muhammad Fito Bayubaskara. These pictures were taken using a digital camera (Nikon D3000) at the Academia Sinica Biotechnology Center in Southern Taiwan (Tainan, Taiwan) in 2021-2022.

  • 2022 Vol.39 No.4
    Selection of a histidine auxotrophic Marchantia polymorpha strain with an auxotrophic selective marker

    A histidine auxotrophic Marchantia polymorpha strain was generated using CRISPR/Cas9-mediated genome editing, which can be used for biocontainment. An auxotrophic selective marker gene applicable to the auxotrophic strain was also developed to select transformants without antibiotic selection. The cover photograph shows a regenerated thallus transformed with Agrobacterium tumefaciens harboring a binary vector pMpGWBhis03-Citrine-NLS that encodes a fluorescent protein and the auxotrophic selective marker protein. Green and red colors indicate fluorescence from the fluorescent protein and chloroplasts, respectively. (See Fukushima and Kodama, pp. 345–354)
    This photograph was taken by Tatsushi Fukushima at Utsunomiya University (Tochigi, Japan) using an MZ16F stereo fluorescence microscope (Leica Microsystems) and a DP73 digital camera (Olympus).

  • 2022 Vol.39 No.3
    Establishment of an efficient transformation method of garden stock using a callus formation chemical inducer

    Garden stock (Matthiola incana) is an important floricultural plant that blooms from winter to spring. This study successfully obtained stable transgenic plants from M. incana (Tanahara et al., pp. 273–280). The leaf sections were cocultivated with the Agrobacterium tumefaciens GV3101 for 5 days, and then obtained hygromycin-resistant calli in a selection medium supplemented with 12.5 µM fipexide (FPX). Then, the transgenic calli were transferred to shoot formation medium. This protocol achieved a 0.7% transformation frequency. FPX is considered a breakthrough for establishing the transformation protocol of M. incana.
    Location: Faculty of Agriculture, Shizuoka University (836 Ohya, Suruga-ku, Shizuoka, Japan)
    Photography equipment: CASIO EXILM EX-ZR850

  • 2022 Vol.39 No.2
    Comparison of constitutive promoter activities and development of maize ubiquitin promoter- and Gateway-based binary vectors for rice

    Transgenic rice seeds segregating proUBQ:GFP (left) and pro35S:GFP (right) at T1 generation. Strong GFP signals were observed in proUBQ:GFP, indicating the activity of this promoter is stable in rice. On the other hand, pro35S:GFP was frequently silenced in rice. Using this ubiquitin promoter from maize, a simple series of binary vectors for rice with gateway system was developed (See Tsuda et al., pp. 139–146). Seeds were illuminated using a blue LED and the photograph was taken by a digital camera (Olympus TG-6) with a GFP filter.