Evidence map›Paper›PMID 30742611›Full record

ArticlePLoS biology2019

Contingency in the convergent evolution of a regulatory network: Dosage compensation in Drosophila.

Christopher Ellison, Doris Bachtrog

Abstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  10. Review
  11. Epigenetics drive the evolution of sex chromosomes in animals and plants.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
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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

2 authors.

Christopher EllisonDepartment of Integrative Biology, University of California Berkeley, Berkeley, California, United States of America.
Doris BachtrogDepartment of Integrative Biology, University of California Berkeley, Berkeley, California, United States of America.ORCID 0000-0001-9724-9467

Funding

The formation of Heterochromatin on evolving Y chromosomesR01GM101255 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Doris Bachtrog · 2015 to 2026
$4.9M
The evolution of dosage compensation in DrosophilaR01GM076007 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BACHTROG, DORIS · 2006 to 2020
$3.6M
"Gene Trafficking on an Evolving X Chromosome in Drosophila"R01GM093182 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BACHTROG, DORIS · 2010 to 2017
$2.7M
NIGMS NIH HHS R01 GM076007NIGMS NIH HHS R01 GM093182NIGMS NIH HHS R01 GM101255
6 · The paper itself

Abstract

The repeatability or predictability of evolution is a central question in evolutionary biology and most often addressed in experimental evolution studies. Here, we infer how genetically heterogeneous natural systems acquire the same molecular changes to address how genomic background affects adaptation in natural populations. In particular, we take advantage of independently formed neo-sex chromosomes in Drosophila species that have evolved dosage compensation by co-opting the dosage-compensation male-specific lethal (MSL) complex to study the mutational paths that have led to the acquisition of hundreds of novel binding sites for the MSL complex in different species. This complex recognizes a conserved 21-bp GA-rich sequence motif that is enriched on the X chromosome, and newly formed X chromosomes recruit the MSL complex by de novo acquisition of this binding motif. We identify recently formed sex chromosomes in the D. melanica and D. robusta species groups by genome sequencing and generate genomic occupancy maps of the MSL complex to infer the location of novel binding sites. We find that diverse mutational paths were utilized in each species to evolve hundreds of de novo binding motifs along the neo-X, including expansions of microsatellites and transposable element (TE) insertions. However, the propensity to utilize a particular mutational path differs between independently formed X chromosomes and appears to be contingent on genomic properties of that species, such as simple repeat or TE density. This establishes the "genomic environment" as an important determinant in predicting the outcome of evolutionary adaptations.

Indexed as

Dosage Compensation, GeneticEvolution, MolecularGene Regulatory NetworksAnimalsBase SequenceBinding SitesChromatinConserved SequenceDrosophila melanogasterDrosophila ProteinsFemaleMaleMolecular Sequence AnnotationMutationNucleotide MotifsPhylogenyChromatinDrosophila Proteins

Identifiers

PMID30742611
PMCPMC6417741

What OpenQuestion holds

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Read underepoch 390

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.