Evidence map›Paper›PMID 32640989›Full record

ArticleBMC plant biology2020

Degradation of key photosynthetic genes in the critically endangered semi-aquatic flowering plant Saniculiphyllum guangxiense (Saxifragaceae).

Ryan A Folk, Neeka Sewnath, Chun-Lei Xiang, Brandon T Sinn, Robert P Guralnick

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Complete chloroplast genome sequence and phylogenetic analysis ofMitochondrial DNA. Part B, Resources · 2026
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  6. Loss of plastidComputational and structural biotechnology journal · 2023
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  7. Article
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  9. The complete plastome sequence ofMitochondrial DNA. Part B, Resources · 2023
    Article
  10. Article
  11. On the Edge of Dispensability, the ChloroplastInternational journal of molecular sciences · 2021
    Review
  12. Article
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 4 institutions in 2 countries.

Ryan A FolkDepartment of Biological Sciences, Mississippi State University, Mississippi, Mississippi State, USA. rfolk@biology.msstate.edu.ORCID http://orcid.org/0000-0002-5333-9273
Neeka SewnathFlorida Museum of Natural History, University of Florida, Gainesville, Florida, USA.
Chun-Lei XiangCAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, P. R. China.
Brandon T SinnDepartment of Biology & Earth Science, Otterbein University, Westerville, OH, USA.
Robert P GuralnickFlorida Museum of Natural History, University of Florida, Gainesville, Florida, USA.
Florida Museum of Natural History · USKunming Institute of Botany · CNMississippi State University · USOtterbein University · US

Funding

Division of Biological Infrastructure 1523667
6 · The paper itself

Abstract

backgroundPlastid gene loss and pseudogenization has been widely documented in parasitic and mycoheterotrophic plants, which have relaxed selective constraints on photosynthetic function. More enigmatic are sporadic reports of pseudogenization and loss of important photosynthesis genes in lineages thought to be fully photosynthetic. Here we report the complete plastid genome of Saniculiphyllum guangxiense, a critically endangered and phylogenetically isolated plant lineage, along with genomic evidence of reduced chloroplast function. We also report 22 additional plastid genomes representing the diversity of its containing clade Saxifragales, characterizing gene content and placing variation in a broader phylogenetic context.

resultsWe find that the plastid genome of Saniculiphyllum has experienced pseudogenization of five genes of the ndh complex (ndhA, ndhB, ndhD, ndhF, and ndhK), previously reported in flowering plants with an aquatic habit, as well as the surprising pseudogenization of two genes more central to photosynthesis (ccsA and cemA), contrasting with strong phylogenetic conservatism of plastid gene content in all other sampled Saxifragales. These genes participate in photooxidative protection, cytochrome synthesis, and carbon uptake. Nuclear paralogs exist for all seven plastid pseudogenes, yet these are also unlikely to be functional.

conclusionsSaniculiphyllum appears to represent the greatest degree of plastid gene loss observed to date in any fully photosynthetic lineage, perhaps related to its extreme habitat specialization, yet plastid genome length, structure, and substitution rate are within the variation previously reported for photosynthetic plants. These results highlight the increasingly appreciated dynamism of plastid genomes, otherwise highly conserved across a billion years of green plant evolution, in plants with highly specialized life history traits.

Indexed as

ChloroplastsEndangered SpeciesGenome, PlastidOrganellesPhotosynthesisPhylogenyPlant ProteinsPlastidsPseudogenesSaxifragaceaePlant ProteinsOrganellePlastid genomePlastomePseudogeneSaniculiphyllumSaxifragaceae

Identifiers

PMID32640989
PMCPMC7346412
OpenAlexW3041856787

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.