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Venn, B.

Publications and source records attributed to Venn, B..

2 recordsLinked to original sources

Systems-wide Analysis Revealed Shared and Unique Responses to Moderate and Acute High Temperatures in the Green Alga Chlamydomonas reinhardtii

Different intensities of high temperatures affect the growth of photosynthetic cells in nature. To elucidate the underlying mechanisms, we cultivated the unicellular green alga Chlamydomonas reinhardtii under highly controlled photobioreactor conditions and revealed systems-wide shared and unique responses to 24-hour moderate (35{degrees}C) and acute (40{degrees}C) high temperatures and subsequent recovery at 25{degrees}C. We identified previously overlooked unique elements in response to moderate high temperature. Heat at 35{degrees}C transiently arrested the cell cycle followed by partial synchronization, up-regulated transcripts/proteins involved in gluconeogenesis/glyoxylate-cycle for carbon uptake, promoted growth, and increased starch accumulation. Heat at 40{degrees}C arrested the cell cycle, inhibited growth, resulting in carbon uptake over usage and increased starch accumulation. Both high temperatures induced photoprotection, while 40{degrees}C decreased photosynthetic efficiency, distorted thylakoid/pyrenoid ultrastructure, and affected the carbon concentrating mechanism. We demonstrated increased transcript/protein correlation during both heat treatments, suggesting reduced post-transcriptional regulation during heat may help coordinate heat tolerance activities efficiently. During recovery after both heat treatments, transcripts/proteins related to DNA synthesis increased while those involved in photosynthetic light reactions decreased. We propose down-regulating photosynthetic light reactions during DNA replication benefits cell cycle resumption by reducing ROS production. Our results provide potential targets to increase thermotolerance in algae and crops.

cell biology

Complexome profiling on the lpa2 mutant reveals insights into PSII biogenesis and new PSII associated proteins

We have identified the homolog of LOW PSII ACCUMULATION 2 (LPA2) in Chlamydomonas. A Chlamydomonas lpa2 mutant grew slower in low light and was hypersensitive to high light. PSII maximum quantum efficiency was reduced by 38%. Synthesis and stability of newly made PSII core subunits D1, D2, CP43, and CP47 were not impaired. Complexome profiling revealed that in the mutant CP43 was reduced to [~]23%, D1, D2, and CP47 to [~]30% of wild-type levels, while small PSII core subunits and components of the oxygen evolving complex were reduced at most by factor two. PSII supercomplexes, dimers, and monomers were reduced to 7%, 26%, and 60% of wild-type levels, while RC47 was increased [~]6-fold. Our data indicate that LPA2 acts at a step during PSII assembly without which PSII monomers and especially further assemblies become intrinsically unstable and prone to degradation. Levels of ATP synthase and LHCII were 29% and 27% higher in the mutant than in the wild type, whereas levels of the cytochrome b6f complex were unaltered. While the abundance of PSI core subunits and antennae hardly changed, LHCI antennae were more disconnected in the lpa2 mutant, presumably as an adaptive response to reduce excitation of PSI. The disconnection of LHCA2,9 together with PSAH and PSAG was the prime response, but independent and additional disconnection of LHCA1,3-8 along with PSAK occurred as well. Finally, based on co-migration profiles, we identified three novel putative PSII associated proteins with potential roles in regulating PSII complex dynamics, assembly, and chlorophyll breakdown. One-sentence summaryWe provide evidence that the Chlamydomonas LPA2 homolog acts at a step in PSII biogenesis without which PSII monomers and further assemblies become unstable and prone to degradation.

plant biology