Evidence map›Paper›PMID 23303190›Full record

ArticleThe Journal of biological chemistry2013

Novel thylakoid membrane GreenCut protein CPLD38 impacts accumulation of the cytochrome b6f complex and associated regulatory processes.

Mark L Heinnickel, Jean Alric, Tyler Wittkopp, Wenqiang Yang, Claudia Catalanotti, Rachel Dent, Krishna K Niyogi, Francis-Andre Wollman, Arthur R Grossman

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Functional Genomics Screening inEnvironmental science & technology · 2026
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  8. A Rubisco-binding protein is required for normal pyrenoid number and starch sheath morphology inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Article
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  11. A repeat protein links Rubisco to form the eukaryotic carbon-concentrating organelle.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  12. Tetratricopeptide repeat protein protects photosystem I from oxidative disruption during assembly.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  13. Article
  14. Critical role of Chlamydomonas reinhardtii ferredoxin-5 in maintaining membrane structure and dark metabolism.Proceedings of the National Academy of Sciences of the United States of America · 2015
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  19. Review
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

9 authors at 3 institutions in 2 countries.

Mark L HeinnickelDepartment of Plant Biology, Carnegie Institute for Science, Stanford, California 94305, USA. mlh300@stanford.edu
Jean Alric
Tyler Wittkopp
Wenqiang Yang
Claudia Catalanotti
Rachel Dent
Krishna K Niyogi
Francis-Andre Wollman
Arthur R Grossman
Carnegie Institution for Science · USCentre National de la Recherche Scientifique · FRHoward Hughes Medical Institute · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Based on previous comparative genomic analyses, a set of nearly 600 polypeptides was identified that is present in green algae and flowering and nonflowering plants but is not present (or is highly diverged) in nonphotosynthetic organisms. The gene encoding one of these "GreenCut" proteins, CPLD38, is in the same operon as ndhL in most cyanobacteria; the NdhL protein is part of a complex essential for cyanobacterial respiration. A cpld38 mutant of Chlamydomonas reinhardtii does not grow on minimal medium, is high light-sensitive under photoheterotrophic conditions, has lower accumulation of photosynthetic complexes, reduced photosynthetic electron flow to P700(+), and reduced photochemical efficiency of photosystem II (ΦPSII); these phenotypes are rescued by a wild-type copy of CPLD38. Single turnover flash experiments and biochemical analyses demonstrated that cytochrome b6f function was severely compromised, and the levels of transcripts and polypeptide subunits of the cytochrome b6f complex were also significantly lower in the cpld38 mutant. Furthermore, subunits of the cytochrome b6f complex in mutant cells turned over much more rapidly than in wild-type cells. Interestingly, PTOX2 and NDA2, two major proteins involved in chlororespiration, were more than 5-fold higher in mutants relative to wild-type cells, suggesting a shift in the cpld38 mutant from photosynthesis toward chlororespiratory metabolism, which is supported by experiments that quantify the reduction state of the plastoquinone pool. Together, these findings support the hypothesis that CPLD38 impacts the stability of the cytochrome b6f complex and possibly plays a role in balancing redox inputs to the quinone pool from photosynthesis and chlororespiration.

Indexed as

Chlamydomonas reinhardtiiChlorophyllChloroplast Proton-Translocating ATPasesCytochrome b6f ComplexCytochromes b6Cytochromes fElectron TransportGene ExpressionImmunoblottingLightMutationOxidation-ReductionPhotosynthesisPhotosynthetic Reaction Center Complex ProteinsPhotosystem II Protein ComplexPhotosystem I Protein ComplexChlorophyllChloroplast Proton-Translocating ATPasesCytochrome b6f ComplexCytochromes b6Cytochromes fPhotosynthetic Reaction Center Complex ProteinsPhotosystem II Protein ComplexPhotosystem I Protein ComplexPlastoquinoneThylakoid Membrane Proteins

Identifiers

PMID23303190
PMCPMC3591612
OpenAlexW2037237554

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.