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Mulo, P.

Publications and source records attributed to Mulo, P..

2 recordsLinked to original sources

Daily Heat Stress Induces Accumulation of Non-functional PSII-LHCII and Donor-side Limitation of PSI via Downregulation of the Cyt bf Complex in Arabidopsis thaliana

The rapidly warming climate is driving increasingly frequent and intense heat waves worldwide, posing major challenges to plant metabolism and growth. Despite the central role of photosynthesis in plant growth, the effects of prolonged heat stress on the primary reactions of photosynthesis remain poorly understood. Here, we studied how long-term heat exposure affects growth and photosynthetic performance in the model plant Arabidopsis thaliana. Plants were exposed daily to high temperature (38{degrees}C) for four hours throughout the growth period. PSII-LHCII complexes remained structurally intact, but {Delta}F/Fm, electron transfer rate (ETRII) and proportion of open reaction centers (qL) were lower under prolonged heat. Strikingly, the content of the Cytochrome b6f complex, which mediates electron transfer between photosystems, was reduced by 30-40%. Consequently, donor-side limitation of PSI was higher and the overall PSI electron transfer rate (ETRI) was lower under long-term heat. Further, carbon assimilation was significantly lower under long-term heat exposure, but PSI acceptor side limitation was not affected. We propose that downregulation of the cytochrome b6f complex restricts electron delivery to PSI, thereby preventing PSI over-reduction due to reduced carbon assimilation. Summary statementHeat-acclimated Arabidopsis thaliana plants accumulate non-functional PSII-LHCII supercomplexes. PSI complex is protected against over-reduction by restricting electron flow from Cyt b6f as an acclimatory response.

plant biology↗

The Arabidopsis NOT4A E3 ligase coordinates PGR3 expression to regulate chloroplast protein translation

Chloroplast function requires the coordinated action of nuclear- and chloroplast-derived proteins, including several hundred nuclear-encoded pentatricopeptide repeat (PPR) proteins that regulate plastid mRNA metabolism. Despite their large number and importance, regulatory mechanisms controlling PPR expression are poorly understood. Here we show that the Arabidopsis NOT4A ubiquitin-ligase positively regulates PROTON GRADIENT 3 (PGR3), a PPR protein required for translating 30S ribosome subunits and several thylakoid-localised photosynthetic components within chloroplasts. Loss of NOT4A function leads to a strong depletion of plastid ribosomes, which reduces mRNA translation and negatively impacts photosynthetic capacity, causing pale-yellow and slow-growth phenotypes. Quantitative transcriptome and proteome analyses reveal that these defects are due to a lack of PGR3 expression in not4a, and we show that normal plastid function is restored through transgenic PGR3 expression. Our work identifies NOT4A as crucial for ensuring robust photosynthetic function during development and stress-response, through modulating PGR3 levels to coordinate chloroplast protein synthesis.

plant biology↗