Evidence map›Paper›PMID 35902820›Full record

ArticleBMC ecology and evolution2022

Trichomes on female reproductive tract: rapid diversification and underlying gene regulatory network in Drosophila suzukii and its related species.

Kentaro M Tanaka, Kanoko Takahashi, Gavin Rice, Mark Rebeiz, Yoshitaka Kamimura, Aya Takahashi

Open access · goldAbstract read
In one paragraph

Article in BMC ecology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

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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 3 institutions in 2 countries.

Kentaro M Tanaka *Department of Biological Sciences, Tokyo Metropolitan University, 192-0397, Hachioji, Japan.
Kanoko Takahashi *Department of Biological Sciences, Tokyo Metropolitan University, 192-0397, Hachioji, Japan.
Gavin RiceDepartment of Biological Sciences, University of Pittsburgh, 15260, Pittsburgh, PA, USA.
Mark RebeizDepartment of Biological Sciences, University of Pittsburgh, 15260, Pittsburgh, PA, USA.
Yoshitaka KamimuraDepartment of Biology, Keio University, 233-8521, Yokohama, Japan.
Aya TakahashiDepartment of Biological Sciences, Tokyo Metropolitan University, 192-0397, Hachioji, Japan. ayat@tmu.ac.jp.
Tokyo Metropolitan University · JPUniversity of Pittsburgh · USKeio University · JP

Funding

Examining the re-use and specialization of an organ-forming gene regulatory networkR21HD104956 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REBEIZ, MARK J · 2021 to 2022
$433k
NICHD NIH HHS R21 HD104956
6 · The paper itself

Abstract

backgroundThe ovipositors of some insects are external female genitalia, which have their primary function to deliver eggs. Drosophila suzukii and its sibling species D. subpulchrella are known to have acquired highly sclerotized and enlarged ovipositors upon their shifts in oviposition sites from rotting to ripening fruits. Inside the ovipositor plates, there are scale-like polarized protrusions termed "oviprovector scales" that are likely to aid the mechanical movement of the eggs. The size and spatial distribution of the scales need to be rearranged following the divergence of the ovipositors. In this study, we examined the features of the oviprovector scales in D. suzukii and its closely related species. We also investigated whether the scales are single-cell protrusions comprised of F-actin under the same conserved gene regulatory network as the well-characterized trichomes on the larval cuticular surface.

resultsThe oviprovector scales of D. suzukii and D. subpulchrella were distinct in size and spatial arrangement compared to those of D. biarmipes and other closely related species. The scale numbers also varied greatly among these species. The comparisons of the size of the scales suggested a possibility that the apical cell area of the oviprovector has expanded upon the elongation of the ovipositor plates in these species. Our transcriptome analysis revealed that 43 out of the 46 genes known to be involved in the trichome gene regulatory network are expressed in the developing female genitalia of D. suzukii and D. subpulchrella. The presence of Shavenbaby (Svb) or svb was detected in the inner cavity of the developing ovipositors of D. melanogaster, D. suzukii, and D. subpulchrella. Also, shavenoid (sha) was expressed in the corresponding patterns in the developing ovipositors and showed differential expression levels between D. suzukii and D. subpulchrella at 48 h APF.

conclusionsThe oviprovector scales have divergent size and spatial arrangements among species. Therefore, these scales may represent a rapidly diversifying morphological trait of the female reproductive tract reflecting ecological contexts. Furthermore, our results showed that the gene regulatory network underlying trichome formation is also utilized to develop the rapidly evolving trichomes on the oviprovectors of these flies.

Indexed as

DrosophilaTrichomesAnimalsBiological EvolutionDrosophila melanogasterFemaleGene Regulatory NetworksGenitalia, FemaleGene regulatory networkOvipositorOviprovector scaleshavenbabyshavenoidTrichome

Identifiers

PMID35902820
PMCPMC9331688
OpenAlexW4288080664

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LicenceCC BY
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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.