Limiting etioplast gene expression induces apical hook twisting during skotomorphogenesis of Arabidopsis seedlings

Author:

Sajib Salek Ahmed12,Grübler Björn3,Oukacine Cylia12,Delannoy Etienne12,Courtois Florence3,Mauve Caroline12,Lurin Claire12,Gakière Bertrand12,Pfannschmidt Thomas4,Merendino Livia12ORCID

Affiliation:

1. Institute of Plant Sciences Paris‐Saclay (IPS2) Université Paris‐Saclay, CNRS, INRAE, Université Evry 91190 Gif sur Yvette France

2. Institute of Plant Sciences Paris‐Saclay (IPS2) Université Paris‐Cité, CNRS, INRAE 91190 Gif sur Yvette France

3. University of Grenoble Alpes, CNRS, INRAE, CEA, IRIG‐LPCV 38000 Grenoble France

4. Institut for Botany, Plant Physiology Leibniz University Hannover Herrenhäuser Str. 2 30419 Hannover Germany

Abstract

SUMMARYWhen 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.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Cell Biology,Plant Science,Genetics

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