Fang Xue, Zhao Lili, Li Jian, Ma Zhiwen, Zhang Feng, Zheng Pengpeng, Wang Ziyu, Liu Yongsheng, Wang Lihuan
Anhui Province Key Laboratory of Horticultural Crop Quality Biology, School of Horticulture, Anhui Agricultural University, Hefei, 230036, China.
Ministry of Education Key Laboratory for Bio-Resource and Eco-Environment, College of Life Science, State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, 610064, Sichuan, China.
Planta. 2024 Dec 18;261(1):17. doi: 10.1007/s00425-024-04592-y.
This study unravels a new regulatory member (AcGLK1) that regulates chloroplast division by affecting the expression levels of cytoskeletal filamenting temperature-sensitive Z (FtsZ) in Actinidia chinensis. GOLDEN 2-LIKE (GLK) transcription factor members of GARP subfamily play an irreplaceable role in regulating chloroplast biogenesis and development. Here we report the functional characterization of a novel GLK1 homolog (AcGLK1) isolated from kiwifruit (Actinidia chinensis cultivar 'Hongyang'). Transgenic lines overexpressing AcGLK1 (AcGLK1OE) resulted in an increase of chloroplast number, size and nutrients accumulation in a tomato variety Micro-Tom (Solanum lycopersicum). Transcriptomic data revealed a series of DEGs related to chloroplast division, in which a tomato FtsZ1 homolog (SlFtsZ1) was significantly upregulated in the transgenic lines and could be directly activated by AcGLK1. Furthermore, AcGLK1 was shown to transcriptionally activate expression of kiwifruit FtsZ1 homologous genes (Achv4p23g035689 and Achv4p19g029547) through Y1H and GUS assays. Taken together, we provide evidence showing that AcGLK1 promotes chloroplast division probably through positively regulation of the transcription of FtsZ1 homologs.
本研究揭示了一个新的调控成员(AcGLK1),它通过影响中华猕猴桃中细胞骨架丝状温度敏感Z(FtsZ)的表达水平来调控叶绿体分裂。GARP亚家族的GOLDEN 2-LIKE(GLK)转录因子成员在调控叶绿体生物发生和发育中发挥着不可替代的作用。在此,我们报道了从猕猴桃(中华猕猴桃品种‘红阳’)中分离出的一种新型GLK1同源物(AcGLK1)的功能特性。过表达AcGLK1的转基因株系(AcGLK1OE)导致番茄品种Micro-Tom(番茄)中叶绿体数量、大小和营养物质积累增加。转录组数据揭示了一系列与叶绿体分裂相关的差异表达基因(DEG),其中一个番茄FtsZ1同源物(SlFtsZ1)在转基因株系中显著上调,并且可以被AcGLK1直接激活。此外,通过酵母单杂交(Y1H)和β-葡萄糖苷酸酶(GUS)分析表明,AcGLK1可转录激活猕猴桃FtsZ1同源基因(Achv4p23g035689和Achv4p19g029547)的表达。综上所述,我们提供的证据表明,AcGLK1可能通过正向调控FtsZ1同源物的转录来促进叶绿体分裂。