Evidence map›Paper›PMID 32719473›Full record

ArticleNature plants2020

Multi-omics reveals mechanisms of total resistance to extreme illumination of a desert alga.

Haim Treves, Beata Siemiatkowska, Urszula Luzarowska, Omer Murik, Noe Fernandez-Pozo, Thiago Alexandre Moraes, Alexander Erban, Ute Armbruster, Yariv Brotman, Joachim Kopka and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature plants, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Haim TrevesMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany. trebes@mpimp-golm.mpg.de.ORCID http://orcid.org/0000-0002-3431-6965
Beata SiemiatkowskaMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.
Urszula LuzarowskaMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.
Omer MurikDepartment of Plant & Environmental Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
Noe Fernandez-PozoPlant Cell Biology, Department of Biology, University of Marburg, Marburg, Germany.
Thiago Alexandre MoraesMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.ORCID http://orcid.org/0000-0002-7156-6947
Alexander ErbanMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.ORCID http://orcid.org/0000-0003-1794-588X
Ute ArmbrusterMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.
Yariv BrotmanMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.
Joachim KopkaMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.ORCID http://orcid.org/0000-0001-9675-4883
Stefan Andreas RensingPlant Cell Biology, Department of Biology, University of Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-0225-873X
Jedrzej SzymanskiDepartment of Network Analysis and Modelling, IPK, Gatersleben, Germany.ORCID http://orcid.org/0000-0003-1086-0920
Mark StittMax Planck Institute for Molecular Plant Physiology, Potsdam, Germany.ORCID http://orcid.org/0000-0002-4900-1763

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The unparalleled performance of Chlorella ohadii under irradiances of twice full sunlight underlines the gaps in our understanding of how the photosynthetic machinery operates, and what sets its upper functional limit. Rather than succumbing to photodamage under extreme irradiance, unique features of photosystem II function allow C. ohadii to maintain high rates of photosynthesis and growth, accompanied by major changes in composition and cellular structure. This remarkable resilience allowed us to investigate the systems response of photosynthesis and growth to extreme illumination in a metabolically active cell. Using redox proteomics, transcriptomics, metabolomics and lipidomics, we explored the cellular mechanisms that promote dissipation of excess redox energy, protein S-glutathionylation, inorganic carbon concentration, lipid and starch accumulation, and thylakoid stacking. C. ohadii possesses a readily available capacity to utilize a sudden excess of reducing power and carbon for growth and reserve formation, and post-translational redox regulation plays a pivotal role in this rapid response. Frequently the response in C. ohadii deviated from that of model species, reflecting its life history in desert sand crusts. Comparative global and case-specific analyses provided insights into the potential evolutionary role of effective reductant utilization in this extreme resistance of C. ohadii to extreme irradiation.

Indexed as

Algal ProteinsChlorellaDesert ClimateGene Expression ProfilingLipidomicsMetabolomicsOxidation-ReductionPhotosynthesisPhotosystem II Protein ComplexProteomicsAlgal ProteinsPhotosystem II Protein Complex

Identifiers

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.