Fast and global reorganization of the chloroplast protein biogenesis network during heat acclimation

Author:

Trösch Raphael12ORCID,Ries Fabian1ORCID,Westrich Lisa Désirée1ORCID,Gao Yang2ORCID,Herkt Claudia1ORCID,Hoppstädter Julia1ORCID,Heck-Roth Johannes1ORCID,Mustas Matthieu3ORCID,Scheuring David4ORCID,Choquet Yves3ORCID,Räschle Markus5ORCID,Zoschke Reimo2ORCID,Willmund Felix1ORCID

Affiliation:

1. Molecular Genetics of Eukaryotes, University of Kaiserslautern, Kaiserslautern 67663, Germany

2. Max Planck Institute of Molecular Plant Physiology, Potsdam-Golm 14476, Germany

3. Biologie du Chloroplaste et Perception de la Lumieère Chez les Microalgues, Institut de Biologie Physico-Chimique, UMR CNRS/UPMC, Paris 7141, France

4. Plant Pathology, University of Kaiserslautern, Kaiserslautern 67663, Germany

5. Molecular Genetics, University of Kaiserslautern, Kaiserslautern 67663, Germany

Abstract

Abstract Photosynthesis is a central determinant of plant biomass production, but its homeostasis is increasingly challenged by heat. Little is known about the sensitive regulatory principles involved in heat acclimation that underly the biogenesis and repair of chloroplast-encoded core subunits of photosynthetic complexes. Employing time-resolved ribosome and transcript profiling together with selective ribosome proteomics, we systematically deciphered these processes in chloroplasts of Chlamydomonas reinhardtii. We revealed protein biosynthesis and altered translation elongation as central processes for heat acclimation and showed that these principles are conserved between the alga and the flowering plant Nicotiana tabacum. Short-term heat exposure resulted in specific translational repression of chlorophyll a-containing core antenna proteins of photosystems I and II. Furthermore, translocation of ribosome nascent chain complexes to thylakoid membranes was affected, as reflected by the increased accumulation of stromal cpSRP54-bound ribosomes. The successful recovery of synthesizing these proteins under prolonged acclimation of nonlethal heat conditions was associated with specific changes of the co-translational protein interaction network, including increased ribosome association of chlorophyll biogenesis enzymes and acclimation factors responsible for complex assembly. We hypothesize that co-translational cofactor binding and targeting might be bottlenecks under heat but become optimized upon heat acclimation to sustain correct co-translational protein complex assembly.

Funder

Carl-Zeiss fellowship to F.R., the Deutsche Forschungsgemeinschaft

Forschungsschwerpunkt BioComp to D.S. and F.W.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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