TY - JOUR
T1 - Establishing an efficient protoplast transient expression system for investigation of floral thermogenesis in aroids
AU - Maekawa, Haruhiko
AU - Otsubo, Miyabi
AU - Sato, Mitsuhiko P.
AU - Takahashi, Tomoko
AU - Mizoguchi, Koichiro
AU - Koyamatsu, Daiki
AU - Inaba, Takehito
AU - Ito-Inaba, Yasuko
N1 - Funding Information:
We thank Yoko Katayama (University of Miyazaki) for their assistance in the cultivation of skunk cabbage plants. This work was supported by a Grant-in-Aid for Scientific Research (grant no. 20H02917 to Y.I.-I., and grant nos. 18H02169 and 20K21282 to T. I.), by the Takeda Science Foundation, and by the Sasakawa Scientific Research Grant from The Japan Science Society.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/1
Y1 - 2022/1
N2 - Key message: Floral thermogenesis is an important reproductive strategy for attracting pollinators. We developed essential biological tools for studying floral thermogenesis using two species of thermogenic aroids,Symplocarpus renifolius and Alocasia odora. Abstract: Aroids contain many species with intense heat-producing abilities in their inflorescences. Several genes have been proposed to be involved in thermogenesis of these species, but biological tools for gene functional analyses are lacking. In this study, we aimed to develop a protoplast-based transient expression (PTE) system for the study of thermogenic aroids. Initially, we focused on skunk cabbage (Symplocarpus renifolius) because of its ability to produce intense as well as durable heat. In this plant, leaf protoplasts were isolated from potted and shoot tip-cultured plants with high efficiency (ca. 1.0 × 105/g fresh weight), and more than half of these protoplasts were successfully transfected. Using this PTE system, we determined the protein localization of three mitochondrial energy-dissipating proteins, SrAOX, SrUCPA, and SrNDA1, fused to green fluorescent protein (GFP). These three GFP-fused proteins were localized in MitoTracker-stained mitochondria in leaf protoplasts, although the green fluorescent particles in protoplasts expressing SrUCPA-GFP were significantly enlarged. Finally, to assess whether the PTE system established in the leaves of S. renifolius is applicable for floral tissues of thermogenic aroids, inflorescences of S. renifolius and another thermogenic aroid (Alocasia odora) were used. Although protoplasts were successfully isolated from several tissues of the inflorescences, PTE systems worked well only for the protoplasts isolated from the female parts (slightly thermogenic or nonthermogenic) of A. odora inflorescences. Our developed system has a potential to be widely used in inflorescences as well as leaves in thermogenic aroids and therefore may be a useful biological tool for investigating floral thermogenesis.
AB - Key message: Floral thermogenesis is an important reproductive strategy for attracting pollinators. We developed essential biological tools for studying floral thermogenesis using two species of thermogenic aroids,Symplocarpus renifolius and Alocasia odora. Abstract: Aroids contain many species with intense heat-producing abilities in their inflorescences. Several genes have been proposed to be involved in thermogenesis of these species, but biological tools for gene functional analyses are lacking. In this study, we aimed to develop a protoplast-based transient expression (PTE) system for the study of thermogenic aroids. Initially, we focused on skunk cabbage (Symplocarpus renifolius) because of its ability to produce intense as well as durable heat. In this plant, leaf protoplasts were isolated from potted and shoot tip-cultured plants with high efficiency (ca. 1.0 × 105/g fresh weight), and more than half of these protoplasts were successfully transfected. Using this PTE system, we determined the protein localization of three mitochondrial energy-dissipating proteins, SrAOX, SrUCPA, and SrNDA1, fused to green fluorescent protein (GFP). These three GFP-fused proteins were localized in MitoTracker-stained mitochondria in leaf protoplasts, although the green fluorescent particles in protoplasts expressing SrUCPA-GFP were significantly enlarged. Finally, to assess whether the PTE system established in the leaves of S. renifolius is applicable for floral tissues of thermogenic aroids, inflorescences of S. renifolius and another thermogenic aroid (Alocasia odora) were used. Although protoplasts were successfully isolated from several tissues of the inflorescences, PTE systems worked well only for the protoplasts isolated from the female parts (slightly thermogenic or nonthermogenic) of A. odora inflorescences. Our developed system has a potential to be widely used in inflorescences as well as leaves in thermogenic aroids and therefore may be a useful biological tool for investigating floral thermogenesis.
KW - Alocasia odora
KW - Araceae
KW - Inflorescence
KW - Mesophyll protoplast
KW - Protein localization
KW - Symplocarpus renifolius
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UR - http://www.scopus.com/inward/citedby.url?scp=85118143776&partnerID=8YFLogxK
U2 - 10.1007/s00299-021-02806-1
DO - 10.1007/s00299-021-02806-1
M3 - Article
C2 - 34704119
AN - SCOPUS:85118143776
VL - 41
SP - 263
EP - 275
JO - Plant Cell Reports
JF - Plant Cell Reports
SN - 0721-7714
IS - 1
ER -