Shanghai Collaborative Innovation Center of Agri-Seeds, Joint Center for Single Cell Biology, School of Agriculture and Biology, Shanghai Jiao Tong University, 800 Dongchuan Rd., Shanghai 200240, China.
Shanghai Collaborative Innovation Center of Agri-Seeds, Joint Center for Single Cell Biology, School of Agriculture and Biology, Shanghai Jiao Tong University, 800 Dongchuan Rd., Shanghai 200240, China.
Plant Sci. 2024 Jun;343:112053. doi: 10.1016/j.plantsci.2024.112053. Epub 2024 Feb 27.
Retrograde signaling between plastids and the nucleus is vital for chloroplast biogenesis and environmental responses. GENOMES UNCOUPLED1 (GUN1) was proposed to be a central integrator of multiple retrograde signaling pathways in the model plant Arabidopsis thaliana (Arabidopsis). However, the function of GUN1 orthologs in other plant species has not been well studied. Here, we found that many GUN1 orthologs from the Solanaceae family have a short N-terminus before the first pentatricopeptide repeat (PPR) motif which is predicted as intrinsically disordered regions (IDRs). Functional analyses of tomato (Solanum lycopersicum L.) GUN1 (SlGUN1), which does not contain N-terminal IDRs, show that it can complement the GUN phenotype of the Arabidopsis gun1 mutant (Atgun1). However, in contrast to the AtGUN1 protein, which does contain the N-terminal IDRs, the SlGUN1 protein is highly accumulated even after chloroplast biogenesis is completed, suggesting that the N-terminal IDRs may determine the stability of the GUN1 protein. Furthermore, we generated tomato Slgun1 genome-edited mutants via the CRISPR-Cas9 system. The Slgun1 mutants exhibited a typical GUN phenotype under lincomycin (Lin) or norflurazon (NF) treatment. Moreover, Slgun1 mutants are hypersensitive to low concentrations of Lin or NF. Taken together, our results suggest that, although lacking the N-terminal IDRs, SlGUN1 plays conserved roles in plastid retrograde signaling in tomato plants.
质体与核之间的逆行信号转导对于叶绿体的生物发生和环境响应至关重要。GENOMES UNCOUPLED1(GUN1)被认为是拟南芥(Arabidopsis)中多种逆行信号通路的中央整合因子。然而,其他植物物种中 GUN1 同源物的功能尚未得到很好的研究。在这里,我们发现茄科家族的许多 GUN1 同源物在第一个五肽重复(PPR)基序之前有一个短的 N 端,该 N 端预测为无规卷曲区域(IDR)。番茄(Solanum lycopersicum L.)GUN1(SlGUN1)的功能分析表明,它不含有 N 端 IDR,可弥补拟南芥 gun1 突变体(Atgun1)的 GUN 表型。然而,与含有 N 端 IDR 的 AtGUN1 蛋白不同,SlGUN1 蛋白即使在叶绿体生物发生完成后也高度积累,这表明 N 端 IDR 可能决定 GUN1 蛋白的稳定性。此外,我们通过 CRISPR-Cas9 系统生成了番茄 Slgun1 基因组编辑突变体。Slgun1 突变体在林可霉素(Lin)或诺氟唑(NF)处理下表现出典型的 GUN 表型。此外,Slgun1 突变体对低浓度的林可霉素或 NF 敏感。总之,我们的结果表明,尽管缺乏 N 端 IDR,SlGUN1 在番茄植物的质体逆行信号转导中仍发挥保守作用。