Evidence map›Paper›PMID 32282855›Full record

ArticlePloS one2020

Sex-specific expression profiles of ecdysteroid biosynthesis and ecdysone response genes in extreme sexual dimorphism of the mealybug Planococcus kraunhiae (Kuwana).

Miyuki Muramatsu, Tomohiro Tsuji, Sayumi Tanaka, Takahiro Shiotsuki, Akiya Jouraku, Ken Miura, Isabelle Mifom Vea, Chieka Minakuchi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Sex-Biased Gene Expression and Isoform Profile of Brine ShrimpAnimals : an open access journal from MDPI · 2021
    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

8 authors at 3 institutions in 1 country.

Miyuki MuramatsuGraduate School of Bio-Agricultural Sciences, Nagoya University, Nagoya, Japan.
Tomohiro TsujiGraduate School of Bio-Agricultural Sciences, Nagoya University, Nagoya, Japan.
Sayumi TanakaGraduate School of Bio-Agricultural Sciences, Nagoya University, Nagoya, Japan.
Takahiro ShiotsukiFaculty of Life and Environmental Science, Shimane University, Matsue, Japan.
Akiya JourakuInstitute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Japan.
Ken MiuraGraduate School of Bio-Agricultural Sciences, Nagoya University, Nagoya, Japan.
Isabelle Mifom VeaGraduate School of Bio-Agricultural Sciences, Nagoya University, Nagoya, Japan.ORCID 0000-0001-9351-7970
Chieka MinakuchiGraduate School of Bio-Agricultural Sciences, Nagoya University, Nagoya, Japan.ORCID 0000-0001-7992-9565
Nagoya University · JPNational Agriculture and Food Research Organization · JPShimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insect molting hormone (ecdysteroids) and juvenile hormone regulate molting and metamorphic events in a variety of insect species. Mealybugs undergo sexually dimorphic metamorphosis: males develop into winged adults through non-feeding, pupa-like stages called prepupa and pupa, while females emerge as neotenic wingless adults. We previously demonstrated, in the Japanese mealybug Planococcus kraunhiae (Kuwana), that the juvenile hormone titer is higher in males than in females at the end of the juvenile stage, which suggests that juvenile hormone may regulate male-specific adult morphogenesis. Here, we examined the involvement of ecdysteroids in sexually dimorphic metamorphosis. To estimate ecdysteroid titers, quantitative RT-PCR analyses of four Halloween genes encoding for cytochrome P450 monooxygenases in ecdysteroid biosynthesis, i.e., spook, disembodied, shadow and shade, were performed. Overall, their expression levels peaked before each nymphal molt. Transcript levels of spook, disembodied and shadow, genes that catalyze the steps in ecdysteroid biosynthesis in the prothoracic gland, were higher in males from the middle of the second nymphal instar to adult emergence. In contrast, the expression of shade, which was reported to be involved in the conversion of ecdysone into 20-hydroxyecdysone in peripheral tissues, was similar between males and females. These results suggest that ecdysteroid biosynthesis in the prothoracic gland is more active in males than in females, although the final conversion into 20-hydroxyecdysone occurs at similar levels in both sexes. Moreover, expression profiles of ecdysone response genes, ecdysone receptor and ecdysone-induced protein 75B, were also analyzed. Based on these expression profiles, we propose that the changes in ecdysteroid titer differ between males and females, and that high ecdysteroid titer is essential for directing male adult development.

Indexed as

AnimalsCytochrome P-450 Enzyme SystemEcdysoneEcdysteroidsEcdysteroneFemaleGene Expression Regulation, DevelopmentalInsectaInsect ProteinsJuvenile HormonesLarvaMaleMetamorphosis, BiologicalMorphogenesisPupaSex CharacteristicsCytochrome P-450 Enzyme SystemEcdysoneEcdysteroidsEcdysteroneInsect ProteinsJuvenile Hormones

Identifiers

PMID32282855
PMCPMC7153872
OpenAlexW3015919400

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.