Evidence map›Paper›PMID 25725432›Full record

ArticleMolecular biology and evolution2015

Digestive organ in the female reproductive tract borrows genes from multiple organ systems to adopt critical functions.

Camille Meslin, Melissa S Plakke, Aaron B Deutsch, Brandon S Small, Nathan I Morehouse, Nathan L Clark

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
9.0field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 40 citations in OpenAlex.

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  12. Structural complexity and molecular heterogeneity of a butterfly ejaculate reflect a complex history of selection.Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

6 authors at 2 institutions in 2 countries.

Camille MeslinDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh.
Melissa S PlakkeDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh.
Aaron B DeutschDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh.
Brandon S SmallDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh.
Nathan I MorehouseDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh nclark@pitt.edu nim@pitt.edu.
Nathan L ClarkDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh nclark@pitt.edu nim@pitt.edu.
University of Pittsburgh · USInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FR

Funding

Acquisition for Illumina HiSeq 2500S10OD010693 · OD · CORNELL UNIVERSITY · PI GRILLS, GEORGE S. · 2012 to 2012
$590k
NIH HHS 1S10OD010693-01NIH HHS S10 OD010693
6 · The paper itself

Abstract

Persistent adaptive challenges are often met with the evolution of novel physiological traits. Although there are specific examples of single genes providing new physiological functions, studies on the origin of complex organ functions are lacking. One such derived set of complex functions is found in the Lepidopteran bursa copulatrix, an organ within the female reproductive tract that digests nutrients from the male ejaculate or spermatophore. Here, we characterized bursa physiology and the evolutionary mechanisms by which it was equipped with digestive and absorptive functionality. By studying the transcriptome of the bursa and eight other tissues, we revealed a suite of highly expressed and secreted gene products providing the bursa with a combination of stomach-like traits for mechanical and enzymatic digestion of the male spermatophore. By subsequently placing these bursa genes in an evolutionary framework, we found that the vast majority of their novel digestive functions were co-opted by borrowing genes that continue to be expressed in nonreproductive tissues. However, a number of bursa-specific genes have also arisen, some of which represent unique gene families restricted to Lepidoptera and may provide novel bursa-specific functions. This pattern of promiscuous gene borrowing and relatively infrequent evolution of tissue-specific duplicates stands in contrast to studies of the evolution of novelty via single gene co-option. Our results suggest that the evolution of complex organ-level phenotypes may often be enabled (and subsequently constrained) by changes in tissue specificity that allow expression of existing genes in novel contexts, such as reproduction. The extent to which the selective pressures encountered in these novel roles require resolution via duplication and sub/neofunctionalization is likely to be determined by the need for specialized reproductive functionality. Thus, complex physiological phenotypes such as that found in the bursa offer important opportunities for understanding the relative role of pleiotropy and specialization in adaptive evolution.

Indexed as

Genes, InsectAdaptation, PhysiologicalAnimalsAnimal StructuresEvolution, MolecularFemaleGene DuplicationGene Expression RegulationLepidopteraMaleOrgan SpecificityPhenotypePhylogenyPrincipal Component AnalysisReproductionSequence Analysis, RNAbursa copulatrixco-optiondigestionevolutionspermatophoretranscriptome

Identifiers

PMID25725432
PMCPMC4572785
OpenAlexW2110058077

What OpenQuestion holds

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LicenceCC BY-NC
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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.