Evidence map›Paper›PMID 27589960›Full record

ArticleBMC biology2016

Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants.

JunMo Lee, Chung Hyun Cho, Seung In Park, Ji Won Choi, Hyun Suk Song, John A West, Debashish Bhattacharya, Hwan Su Yoon

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
13.1field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 96 citations in OpenAlex.

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  12. Taxonomic reinvestigation of the genusFrontiers in plant science · 2024
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  13. The complete chloroplast genome ofMitochondrial DNA. Part B, Resources · 2024
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  15. WHIRLY protein functions in plants.Food and energy security · 2023
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  16. Article
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  18. Complete plastid genome ofMitochondrial DNA. Part B, Resources · 2021
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  19. Article
  20. OGDA: a comprehensive organelle genome database for algae.Database : the journal of biological databases and curation · 2020
    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

8 authors at 3 institutions in 3 countries.

JunMo LeeDepartment of Biological Sciences, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Chung Hyun ChoDepartment of Biological Sciences, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Seung In ParkDepartment of Biological Sciences, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Ji Won ChoiDepartment of Biological Sciences, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Hyun Suk SongDepartment of Biological Sciences, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
John A WestSchool of Biosciences 2, University of Melbourne, Parkville, VIC, 3010, Australia.
Debashish BhattacharyaDepartment of Ecology, Evolution and Natural Resources, Rutgers University, New Brunswick, NJ, 08901, USA.
Hwan Su YoonDepartment of Biological Sciences, Sungkyunkwan University, Suwon, 16419, Republic of Korea. hsyoon2011@skku.edu.
Sungkyunkwan University · KRRutgers, The State University of New Jersey · USUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe red algae (Rhodophyta) diverged from the green algae and plants (Viridiplantae) over one billion years ago within the kingdom Archaeplastida. These photosynthetic lineages provide an ideal model to study plastid genome reduction in deep time. To this end, we assembled a large dataset of the plastid genomes that were available, including 48 from the red algae (17 complete and three partial genomes produced for this analysis) to elucidate the evolutionary history of these organelles.

resultsWe found extreme conservation of plastid genome architecture in the major lineages of the multicellular Florideophyceae red algae. Only three minor structural types were detected in this group, which are explained by recombination events of the duplicated rDNA operons. A similar high level of structural conservation (although with different gene content) was found in seed plants. Three major plastid genome architectures were identified in representatives of 46 orders of angiosperms and three orders of gymnosperms.

conclusionsOur results provide a comprehensive account of plastid gene loss and rearrangement events involving genome architecture within Archaeplastida and lead to one over-arching conclusion: from an ancestral pool of highly rearranged plastid genomes in red and green algae, the aquatic (Florideophyceae) and terrestrial (seed plants) multicellular lineages display high conservation in plastid genome architecture. This phenomenon correlates with, and could be explained by, the independent and widely divergent (separated by >400 million years) origins of complex sexual cycles and reproductive structures that led to the rapid diversification of these lineages.

Indexed as

Evolution, MolecularGenome, PlastidConserved SequenceCycadopsidaGenetic VariationMagnoliopsidaMultigene FamilyPhylogenyRhodophytaSeedsSyntenyFlorideophyceaeParallel evolutionPlastid genome architectureRhodophytaSeed plants

Identifiers

PMID27589960
PMCPMC5010701
OpenAlexW2509170972

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LicenceCC BY
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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.