Evidence map›Paper›PMID 28859625›Full record

ArticleBMC evolutionary biology2017

Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria.

Robin Koch, Anne Kupczok, Karina Stucken, Judith Ilhan, Katrin Hammerschmidt, Tal Dagan

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2017. 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
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Compensatory Transcriptional Response ofMolecules (Basel, Switzerland) · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Loss of Filamentous Multicellularity inJournal of bacteriology · 2020
    Article
  12. Review
  13. 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

6 authors at 2 institutions in 2 countries.

Robin KochInstitute of General Microbiology, Kiel University, Kiel, Germany.
Anne KupczokInstitute of General Microbiology, Kiel University, Kiel, Germany.
Karina StuckenInstitute of General Microbiology, Kiel University, Kiel, Germany.
Judith IlhanInstitute of General Microbiology, Kiel University, Kiel, Germany.
Katrin HammerschmidtInstitute of General Microbiology, Kiel University, Kiel, Germany.
Tal DaganInstitute of General Microbiology, Kiel University, Kiel, Germany. tdagan@ifam.uni-kiel.de.ORCID 0000-0002-9042-192X
Christian-Albrechts-Universität zu Kiel · DEHochschule für Angewandte Wissenschaften Kiel · DE

Funding

European Research Council 281357
6 · The paper itself

Abstract

backgroundFilamentous cyanobacteria that differentiate multiple cell types are considered the peak of prokaryotic complexity and their evolution has been studied in the context of multicellularity origins. Species that form true-branching filaments exemplify the most complex cyanobacteria. However, the mechanisms underlying the true-branching morphology remain poorly understood despite of several investigations that focused on the identification of novel genes or pathways. An alternative route for the evolution of novel traits is based on existing phenotypic plasticity. According to that scenario - termed genetic assimilation - the fixation of a novel phenotype precedes the fixation of the genotype.

resultsHere we show that the evolution of transcriptional regulatory elements constitutes a major mechanism for the evolution of new traits. We found that supplementation with sucrose reconstitutes the ancestral branchless phenotype of two true-branching Fischerella species and compared the transcription start sites (TSSs) between the two phenotypic states. Our analysis uncovers several orthologous TSSs whose transcription level is correlated with the true-branching phenotype. These TSSs are found in genes that encode components of the septosome and elongasome (e.g., fraC and mreB).

conclusionsThe concept of genetic assimilation supplies a tenable explanation for the evolution of novel traits but testing its feasibility is hindered by the inability to recreate and study the evolution of present-day traits. We present a novel approach to examine transcription data for the plasticity first route and provide evidence for its occurrence during the evolution of complex colony morphology in true-branching cyanobacteria. Our results reveal a route for evolution of the true-branching phenotype in cyanobacteria via modification of the transcription level of pre-existing genes. Our study supplies evidence for the 'plasticity-first' hypothesis and highlights the importance of transcriptional regulation in the evolution of novel traits.

Indexed as

Biological EvolutionRegulatory Sequences, Nucleic AcidCyanobacteriaEvolution, MolecularGene Expression RegulationPhenotypeSucroseTranscription Initiation SiteSucroseComparative transcriptomicsCyanobacterial evolutionGenetic assimilationTrue-branching

Identifiers

PMID28859625
PMCPMC5580265
OpenAlexW2753653404

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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.