Ishikawa Hiroki, Yasuzawa Mana, Koike Nana, Sanjaya Alvin, Moriyama Shota, Nishizawa Aya, Matsuoka Kanae, Sasaki Shun, Kazama Yusuke, Hayashi Yoriko, Abe Tomoko, Fujiwara Makoto T, Itoh Ryuuichi D
Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Tokyo, Japan.
Nishina Center for Accelerator-Based Science, RIKEN, Wako, Japan.
Front Plant Sci. 2020 Jan 15;10:1665. doi: 10.3389/fpls.2019.01665. eCollection 2019.
Recently, a recessive mutant with abundant stromules in leaf epidermal pavement cells was visually screened and isolated. The gene responsible for this mutant phenotype was identified as , a chloroplast division site regulator gene. The mutant allele carried two point mutations (G62R and W700stop) at the N- and C-terminal ends of the coding sequence, respectively. Here, we further characterized and other mutant alleles, and showed that plays a critical role in plastid morphogenesis in all cell types of the leaf epidermis: pavement cells, trichome cells, and guard cells. Transient expression of PARC6 transit peptide (TP) fused to the green fluorescent protein (GFP) in plant cells showed that the G62R mutation has no or little effect on the TP activity of the PARC6 N-terminal region. Then, plastid morphology was microscopically analyzed in the leaf epidermis of wild-type (WT) and mutants (, , and ) with the aid of stroma-targeted fluorescent proteins. In pavement cells, plastids often assumed aberrant grape-like morphology, similar to those in severe plastid division mutants, and . In trichome cells, plastids exhibited extreme grape-like aggregations, without the production of giant plastids (>6 µm diameter), as a general phenotype. In guard cells, plastids exhibited a variety of abnormal phenotypes, including reduced number, enlarged size, and activated stromules, similar to those in and guard cells. Nevertheless, unlike and , exhibited a low number of mini-chloroplasts (< 2 µm diameter) and rarely produced chloroplast-deficient guard cells. Importantly, unlike , the chloroplast division site mutant exhibited WT-like plastid phenotypes in trichome and guard cells. Finally, observation of complementation lines expressing a functional PARC6-GFP protein indicated that PARC6-GFP formed a ring-like structure in both constricting and non-constricting chloroplasts, and that PARC6 dynamically changes its configuration during the process of chloroplast division.
最近,通过视觉筛选分离出了一种在叶片表皮铺板细胞中具有丰富基质小管的隐性突变体。负责这种突变体表型的基因被鉴定为,一个叶绿体分裂位点调节基因。突变等位基因在编码序列的N端和C端分别携带两个点突变(G62R和W700stop)。在这里,我们进一步对和其他突变等位基因进行了表征,并表明在叶片表皮的所有细胞类型:铺板细胞、毛状体细胞和保卫细胞的质体形态发生中起关键作用。在植物细胞中瞬时表达与绿色荧光蛋白(GFP)融合的PARC6转运肽(TP)表明,G62R突变对PARC6 N端区域的TP活性没有或几乎没有影响。然后,借助基质靶向荧光蛋白,在野生型(WT)和突变体(、、和)的叶片表皮中对质体形态进行了显微镜分析。在铺板细胞中,质体常常呈现异常的葡萄状形态,类似于严重质体分裂突变体和中的质体。在毛状体细胞中,质体表现出极端的葡萄状聚集,作为一般表型,不产生巨型质体(直径>6 µm)。在保卫细胞中,质体表现出多种异常表型,包括数量减少、尺寸增大和基质小管活化,类似于和保卫细胞中的表型。然而,与和不同,表现出少量的微型叶绿体(直径<2 µm),很少产生叶绿体缺陷的保卫细胞。重要的是,与不同,叶绿体分裂位点突变体在毛状体和保卫细胞中表现出类似WT的质体表型。最后,对表达功能性PARC6-GFP蛋白的互补系的观察表明,PARC6-GFP在收缩和非收缩叶绿体中均形成环状结构,并且PARC6在叶绿体分裂过程中动态改变其构型。