叶绿体
生物
肌动蛋白
嗜光蛋白
细胞生物学
叶绿体膜
MDia1公司
肌动蛋白重塑
拟南芥
生物物理学
肌动蛋白细胞骨架
细胞骨架
生物化学
基因
细胞
类囊体
突变体
作者
Sam‐Geun Kong,Y. Yamazaki,Akira Shimada,Saku T. Kijima,Keiko Hirose,K. Katoh,Jeongsu Ahn,Hyun‐Geun Song,Jae Hee Han,Takeshi Higa,Akira Takano,Yoshito Nakamura,Noriyuki Suetsugu,Daisuke Kohda,Taro Q.P. Uyeda,Masamitsu Wada
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2023-12-22
卷期号:36 (4): 1159-1181
被引量:1
标识
DOI:10.1093/plcell/koad320
摘要
Plants have unique responses to fluctuating light conditions. One such response involves chloroplast photorelocation movement, which optimizes photosynthesis under weak light by the accumulation of chloroplasts along the periclinal side of the cell, which prevents photodamage under strong light by avoiding chloroplast positioning toward the anticlinal side of the cell. This light-responsive chloroplast movement relies on the reorganization of chloroplast actin (cp-actin) filaments. Previous studies have suggested that CHLOROPLAST UNUSUAL POSITIONING 1 (CHUP1) is essential for chloroplast photorelocation movement as a regulator of cp-actin filaments. In this study, we conducted comprehensive analyses to understand CHUP1 function. Functional, fluorescently tagged CHUP1 colocalized with and was coordinately reorganized with cp-actin filaments on the chloroplast outer envelope during chloroplast movement in Arabidopsis thaliana. CHUP1 distribution was reversibly regulated in a blue light- and phototropin-dependent manner. X-ray crystallography revealed that the CHUP1-C-terminal domain shares structural homology with the formin homology 2 (FH2) domain, despite lacking sequence similarity. Furthermore, the CHUP1-C-terminal domain promoted actin polymerization in the presence of profilin in vitro. Taken together, our findings indicate that CHUP1 is a plant-specific actin polymerization factor that has convergently evolved to assemble cp-actin filaments and enables chloroplast photorelocation movement.
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