Evidence map›Paper›PMID 26976593›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Protein networks identify novel symbiogenetic genes resulting from plastid endosymbiosis.

Raphaël Méheust, Ehud Zelzion, Debashish Bhattacharya, Philippe Lopez, Eric Bapteste

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

  1. Transfer of chloroplastSynthetic and systems biotechnology · 2027
    Article
  2. Article
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  4. Article
  5. Why is primary endosymbiosis so rare?The New phytologist · 2021
    Review
  6. Phylogenomic fingerprinting of tempo and functions of horizontal gene transfer within ochrophytes.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Review
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  12. Verification of theInternational journal of molecular sciences · 2019
    Article
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  15. Review
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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

5 authors at 3 institutions in 2 countries.

Raphaël MéheustUnité Mixte de Recherche 7138 Evolution Paris Seine, Institut de Biologie Paris Seine, Université Pierre et Marie Curie, Centre National de la Recherche Scientifique, Sorbonne Universités, 75005 Paris, France;
Ehud ZelzionDepartment of Ecology, Evolution, and Natural Resources, Rutgers University, New Brunswick, NJ 08901.
Debashish BhattacharyaDepartment of Ecology, Evolution, and Natural Resources, Rutgers University, New Brunswick, NJ 08901.
Philippe LopezUnité Mixte de Recherche 7138 Evolution Paris Seine, Institut de Biologie Paris Seine, Université Pierre et Marie Curie, Centre National de la Recherche Scientifique, Sorbonne Universités, 75005 Paris, France;
Eric BaptesteUnité Mixte de Recherche 7138 Evolution Paris Seine, Institut de Biologie Paris Seine, Université Pierre et Marie Curie, Centre National de la Recherche Scientifique, Sorbonne Universités, 75005 Paris, France; epbapteste@gmail.com.
Institut de Biologie Paris-Seine · FRRutgers, The State University of New Jersey · USSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The integration of foreign genetic information is central to the evolution of eukaryotes, as has been demonstrated for the origin of the Calvin cycle and of the heme and carotenoid biosynthesis pathways in algae and plants. For photosynthetic lineages, this coordination involved three genomes of divergent phylogenetic origins (the nucleus, plastid, and mitochondrion). Major hurdles overcome by the ancestor of these lineages were harnessing the oxygen-evolving organelle, optimizing the use of light, and stabilizing the partnership between the plastid endosymbiont and host through retargeting of proteins to the nascent organelle. Here we used protein similarity networks that can disentangle reticulate gene histories to explore how these significant challenges were met. We discovered a previously hidden component of algal and plant nuclear genomes that originated from the plastid endosymbiont: symbiogenetic genes (S genes). These composite proteins, exclusive to photosynthetic eukaryotes, encode a cyanobacterium-derived domain fused to one of cyanobacterial or another prokaryotic origin and have emerged multiple, independent times during evolution. Transcriptome data demonstrate the existence and expression of S genes across a wide swath of algae and plants, and functional data indicate their involvement in tolerance to oxidative stress, phototropism, and adaptation to nitrogen limitation. Our research demonstrates the "recycling" of genetic information by photosynthetic eukaryotes to generate novel composite genes, many of which function in plastid maintenance.

Indexed as

Evolution, MolecularEukaryotaGene FusionGenome, PlantModels, GeneticMultigene FamilyOxidation-ReductionPhotosynthesisPhylogenyPlantsPlastidsProteinsSequence Homology, Amino AcidSymbiosisProteinsendosymbiosiseukaryote evolutiongene fusionnovel gene originphotosynthesis

Identifiers

PMID26976593
PMCPMC4822624
OpenAlexW2302483547

What OpenQuestion holds

Textmetadata
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.