Department of Biological Sciences, College of Natural Sciences, Kongju National University, Chungnam 32588, Korea.
Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
Plant Cell. 2024 Mar 29;36(4):1159-1181. doi: 10.1093/plcell/koad320.
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.
植物对不断变化的光照条件有独特的反应。其中一种反应涉及叶绿体的光定位运动,通过在细胞的垂周侧积累叶绿体,来优化弱光下的光合作用,同时通过避免叶绿体定位在细胞的垂周侧来防止强光下的光损伤。这种对光的响应的叶绿体运动依赖于叶绿体肌动蛋白(cp-actin)丝的重组。以前的研究表明,质体异常定位蛋白 1(CHUP1)作为 cp-actin 丝的调节剂,对于叶绿体的光定位运动是必不可少的。在这项研究中,我们进行了全面的分析来了解 CHUP1 的功能。功能荧光标记的 CHUP1 在拟南芥叶绿体运动过程中与 cp-actin 丝共定位,并与 cp-actin 丝一起在叶绿体外被上协调重组。CHUP1 的分布以蓝光和向光素依赖的方式可逆调节。X 射线晶体学揭示了 CHUP1-C 端结构域与formin 同源 2(FH2)结构域具有结构同源性,尽管缺乏序列相似性。此外,CHUP1-C 端结构域在存在丝氨酸的情况下促进体外肌动蛋白聚合。总之,我们的研究结果表明,CHUP1 是一种植物特异性的肌动蛋白聚合因子,它已经趋同进化以组装 cp-actin 丝,并使叶绿体光定位运动成为可能。