TY - JOUR
T1 - Phototropin2 contributes to the chloroplast avoidance response at the chloroplast-plasma membrane InterfAce1[CC-by]
AU - Ishishita, Kazuhiro
AU - Higa, Takeshi
AU - Tanaka, Hidekazu
AU - Inoue, Shin Ichiro
AU - Chung, Aeri
AU - Ushijima, Tomokazu
AU - Matsushita, Tomonao
AU - Kinoshita, Toshinori
AU - Nakai, Masato
AU - Wada, Masamitsu
AU - Suetsugu, Noriyuki
AU - Gotoh, Eiji
N1 - Funding Information:
1This work was supported in part by the Japan Society for the Promotion of Science (JSPS; Grants-in-Aid for Scientific Research nos. JP15K18713, JP18K14491, and JP19H04729 to E.G., no. JP15KK0254 and JP19K06721 to N.S., and Grant-in-Aid for a JSPS Research Fellow no. JP17J06717 to T.H.), and by Kyushu University (Young Investigators Award to E.G.), the Ichimura Foundation for New Technology (research grant to E.G.), and the Ohsumi Frontier Science Foundation (research grant to M.W.). 2These authors contributed equally to the article. 3Senior author. 4Author for contact: eiji.gotoh@agr.kyushu-u.ac.jp.
Funding Information:
1This work was supported in part by the Japan Society for the Promotion of Science (JSPS; Grants-in-Aid for Scientific Research nos. JP15K18713, JP18K14491, and JP19H04729 to E.G., no. JP15KK0254 and JP19K06721 to N.S., and Grant-in-Aid for a JSPS Research Fellow no. JP17J06717 to T.H.), and by Kyushu University (Young Investigators Award to E.G.), the Ichimura Foundation for New Technology (research grant to E.G.), and the Ohsumi Frontier Science Foundation (research grant to M.W.). The authors thank Ryota Kiyabu, Jaewook Kim, and Bungo Shirouchi of Kyushu University for valuable discussions. The authors also thank Tomoyo Kusumoto, Yumi Ichikawa, Rika Kunihiro of Kyushu University for technical assistance. We thank the Center for Advanced Instrumental and Educational Support of the Faculty of Agriculture, Kyushu University, for confocal microscopy.
Publisher Copyright:
Copyright © 2020 American Society of Plant Biologists. All rights reserved.
PY - 2020/5
Y1 - 2020/5
N2 - Blue-light-induced chloroplast movements play an important role in maximizing light utilization for photosynthesis in plants. Under a weak light condition, chloroplasts accumulate to the cell surface to capture light efficiently (chloroplast accumulation response). Conversely, chloroplasts escape from strong light and move to the side wall to reduce photodamage (chloroplast avoidance response). The blue light receptor phototropin (phot) regulates these chloroplast movements and optimizes leaf photosynthesis by controlling other responses in addition to chloroplast movements. Seed plants such as Arabidopsis (Arabidopsis thaliana) have phot1 and phot2. They redundantly mediate phototropism, stomatal opening, leaf flattening, and the chloroplast accumulation response. However, the chloroplast avoidance response is induced by strong blue light and regulated primarily by phot2. Phots are localized mainly on the plasma membrane. However, a substantial amount of phot2 resides on the chloroplast outer envelope. Therefore, differentially localized phot2 might have different functions. To determine the functions of plasma membrane- and chloroplast envelope-localized phot2, we tethered it to these structures with their respective targeting signals. Plasma membrane-localized phot2 regulated phototropism, leaf flattening, stomatal opening, and chloroplast movements. Chloroplast envelope-localized phot2 failed to mediate phototropism, leaf flattening, and the chloroplast accumulation response but partially regulated the chloroplast avoidance response and stomatal opening. Based on the present and previous findings, we propose that phot2 localized at the interface between the plasma membrane and the chloroplasts is required for the chloroplast avoidance response and possibly for stomatal opening as well.
AB - Blue-light-induced chloroplast movements play an important role in maximizing light utilization for photosynthesis in plants. Under a weak light condition, chloroplasts accumulate to the cell surface to capture light efficiently (chloroplast accumulation response). Conversely, chloroplasts escape from strong light and move to the side wall to reduce photodamage (chloroplast avoidance response). The blue light receptor phototropin (phot) regulates these chloroplast movements and optimizes leaf photosynthesis by controlling other responses in addition to chloroplast movements. Seed plants such as Arabidopsis (Arabidopsis thaliana) have phot1 and phot2. They redundantly mediate phototropism, stomatal opening, leaf flattening, and the chloroplast accumulation response. However, the chloroplast avoidance response is induced by strong blue light and regulated primarily by phot2. Phots are localized mainly on the plasma membrane. However, a substantial amount of phot2 resides on the chloroplast outer envelope. Therefore, differentially localized phot2 might have different functions. To determine the functions of plasma membrane- and chloroplast envelope-localized phot2, we tethered it to these structures with their respective targeting signals. Plasma membrane-localized phot2 regulated phototropism, leaf flattening, stomatal opening, and chloroplast movements. Chloroplast envelope-localized phot2 failed to mediate phototropism, leaf flattening, and the chloroplast accumulation response but partially regulated the chloroplast avoidance response and stomatal opening. Based on the present and previous findings, we propose that phot2 localized at the interface between the plasma membrane and the chloroplasts is required for the chloroplast avoidance response and possibly for stomatal opening as well.
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U2 - 10.1104/pp.20.00059
DO - 10.1104/pp.20.00059
M3 - Article
C2 - 32193212
AN - SCOPUS:85084721444
SN - 0032-0889
VL - 183
SP - 304
EP - 316
JO - Plant physiology
JF - Plant physiology
IS - 5
ER -