Evidence map›Paper›PMID 35363565›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Layered evolution of gene expression in "superfast" muscles for courtship.

James B Pease, Robert J Driver, David A de la Cerda, Lainy B Day, Willow R Lindsay, Barney A Schlinger, Eric R Schuppe, Christopher N Balakrishnan, Matthew J Fuxjager

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  5. Differential gene reactions reveal drought response strategies in African acacias.The Plant journal : for cell and molecular biology · 2025
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  10. Layered evolution of gene expression in "superfast" muscles for courtship.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

9 authors at 5 institutions in 3 countries.

James B PeaseDepartment of Biology, Wake Forest University, Winston-Salem, NC 27109.ORCID 0000-0003-0125-9156
Robert J DriverDepartment of Biology, East Carolina University, Greenville, NC 27858.ORCID 0000-0002-6950-0607
David A de la CerdaDepartment of Biology, Wake Forest University, Winston-Salem, NC 27109.ORCID 0000-0002-6833-0730
Lainy B DayDepartment of Biology, University of Mississippi, Oxford, MS 38677.ORCID 0000-0002-9122-3044
Willow R LindsayDepartment of Biology, University of Mississippi, Oxford, MS 38677.
Barney A SchlingerDepartment of Integrative Biology and Physiology, University of California, Los Angeles, CA 90095.
Eric R SchuppeDepartment of Biology, Wake Forest University, Winston-Salem, NC 27109.
Christopher N BalakrishnanDepartment of Biology, East Carolina University, Greenville, NC 27858.ORCID 0000-0002-0788-0659
Matthew J FuxjagerDepartment of Ecology, Evolution, and Organismal Biology, Brown University, Providence, RI 02912.ORCID 0000-0003-0591-6854
Wake Forest University · USEast Carolina University · USUniversity of Mississippi · USBrown University · USSmithsonian Tropical Research Institute · PA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying the molecular process of complex trait evolution is a core goal of biology. However, pinpointing the specific context and timing of trait-associated changes within the molecular evolutionary history of an organism remains an elusive goal. We study this topic by exploring the molecular basis of elaborate courtship evolution, which represents an extraordinary example of trait innovation. Within the behaviorally diverse radiation of Central and South American manakin birds, species from two separate lineages beat their wings together using specialized “superfast” muscles to generate a “snap” that helps attract mates. Here, we develop an empirical approach to analyze phylogenetic lineage-specific shifts in gene expression in the key snap-performing muscle and then integrate these findings with comparative transcriptomic sequence analysis. We find that rapid wing displays are associated with changes to a wide range of molecular processes that underlie extreme muscle performance, including changes to calcium trafficking, myocyte homeostasis and metabolism, and hormone action. We furthermore show that these changes occur gradually in a layered manner across the species history, wherein which ancestral genetic changes to many of these molecular systems are built upon by later species-specific shifts that likely finalized the process of display performance adaptation. Our study demonstrates the potential for combining phylogenetic modeling of tissue-specific gene expression shifts with phylogenetic analysis of lineage-specific sequence changes to reveal holistic evolutionary histories of complex traits.

Indexed as

CourtshipFlight, AnimalGene ExpressionMating Preference, AnimalMuscle, SkeletalPasseriformesAnimalsOrgan SpecificityPhylogenybehavioral physiologymanakinmolecular evolutionphylogenomicstranscriptomics

Identifiers

PMID35363565
PMCPMC9168950
OpenAlexW4220671869

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.