Limiting etioplast gene expression induces apical hook twisting during skotomorphogenesis of Arabidopsis seedlings. (3rd March 2023)

• Record Type: Journal Article
• Authors: Sajib, Salek Ahmed; Grübler, Björn; Oukacine, Cylia; Delannoy, Etienne; Courtois, Florence; Mauve, Caroline; Lurin, Claire; Gakière, Bertrand; Pfannschmidt, Thomas; Merendino, Livia
• Is Part Of: Plant journal. Volume 114:Number 2(2023)
• Page Start: 293
• Page End: 309
• Publication Date: 2023-03-03
• Subjects: skotomorphogenesis -- apical hook bending -- plastids -- mitochondria -- gene expression -- reactive oxygen species -- AOX1A -- rifampicin -- spectinomycin -- Arabidopsis thaliana; Plant molecular biology -- Periodicals; Plant cells and tissues -- Periodicals; Botany -- Periodicals; 580
• DOI: 10.1111/tpj.16134
• Languages: English
• ISSNs: 0960-7412

Abstract

SUMMARY: When covered by a layer of soil, seedling development follows a dark‐specific program (skotomorphogenesis). In the dark, seedlings consist of small, non‐green cotyledons, a long hypocotyl, and an apical hook to protect meristematic cells. We recently highlighted the role played by mitochondria in the high energy‐consuming reprogramming of Arabidopsis skotomorphogenesis. Here, the role played by plastids, another energy‐supplying organelle, in skotomorphogenesis is investigated. This study was conducted in dark conditions to exclude light signals so as to better focus on those produced by plastids. It was found that limitation of plastid gene expression (PGE) induced an exaggerated apical hook bending. Inhibition of PGE was obtained at the levels of transcription and translation using the antibiotics rifampicin (RIF) and spectinomycin, respectively, as well as plastid RPOTp RNA polymerase mutants. RIF‐treated seedlings also showed expression induction of marker nuclear genes for mitochondrial stress, perturbation of mitochondrial metabolism, increased ROS levels, and an augmented capacity of oxygen consumption by mitochondrial alternative oxidases (AOXs). AOXs act to prevent overreduction of the mitochondrial electron transport chain. Previously, we reported that AOX1A, the main AOX isoform, is a key component in the developmental response to mitochondrial respiration deficiency. In this work, we suggest the involvement of AOX1A in the response to PGE dysfunction and propose the importance of signaling between plastids and mitochondria. Finally, it was found that seedling architecture reprogramming in response to RIF was independent of canonical organelle retrograde pathways and the ethylene signaling pathway. Significance Statement: In underground germination conditions, seedling development follows a dark‐specific program (skotomorphogenesis); in the dark, seedlings consist of small and non‐green cotyledons, a long hypocotyl, and an apical hook to protect meristematic cells. We show that skotomorphogenesis is reprogrammed when plastid gene expression is perturbed, leading to an exaggeration of apical hook bending. We propose the involvement of the cooperation between plastids and mitochondria, the energy‐supplying organelles of the cell.