Evidence map›Paper›PMID 38366199›Full record

ArticleThe ISME journal2024

The Constructive Black Queen hypothesis: new functions can evolve under conditions favouring gene loss.

Nobuto Takeuchi, Matthew S Fullmer, Danielle J Maddock, Anthony M Poole

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in The ISME journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 2 countries.

Nobuto TakeuchiSchool of Biological Sciences, University of Auckland, Auckland 1010, New Zealand.
Matthew S FullmerSchool of Biological Sciences, University of Auckland, Auckland 1010, New Zealand.
Danielle J MaddockSchool of Biological Sciences, University of Auckland, Auckland 1010, New Zealand.
Anthony M PooleSchool of Biological Sciences, University of Auckland, Auckland 1010, New Zealand.
University of Auckland · NZ

Funding

Faculty of Science Faculty Research Development Fund, University of AucklandRoyal Society of New Zealand Marsden Fund 22-UOA-250School of Biological Sciences Academic Leaders' Fund, University of Auckland
6 · The paper itself

Abstract

Duplication is a major route for the emergence of new gene functions. However, the emergence of new gene functions via this route may be reduced in prokaryotes, as redundant genes are often rapidly purged. In lineages with compact, streamlined genomes, it thus appears challenging for novel function to emerge via duplication and divergence. A further pressure contributing to gene loss occurs under Black Queen dynamics, as cheaters that lose the capacity to produce a public good can instead acquire it from neighbouring producers. We propose that Black Queen dynamics can favour the emergence of new function because, under an emerging Black Queen dynamic, there is high gene redundancy spread across a community of interacting cells. Using computational modelling, we demonstrate that new gene functions can emerge under Black Queen dynamics. This result holds even if there is deletion bias due to low duplication rates and selection against redundant gene copies resulting from the high cost associated with carrying a locus. However, when the public good production costs are high, Black Queen dynamics impede the fixation of new functions. Our results expand the mechanisms by which new gene functions can emerge in prokaryotic systems.

Indexed as

Multigene FamilyProkaryotic CellsEvolution, MolecularBlack Queen hypothesisconstructive neutral evolutiongene duplicationhorizontal gene transfermodellingneofunctionalizationpublic goods

Identifiers

PMID38366199
PMCPMC10942775
OpenAlexW4391151112

What OpenQuestion 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 OpenQuestion graph.