Evidence map›Paper›PMID 22427652›Full record

ArticleThe Journal of biological chemistry2012

Fungal ecdysteroid-22-oxidase, a new tool for manipulating ecdysteroid signaling and insect development.

Manabu Kamimura, Hitoshi Saito, Ryusuke Niwa, Teruyuki Niimi, Kinuko Toyoda, Chihiro Ueno, Yasushi Kanamori, Sachiko Shimura, Makoto Kiuchi

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. 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
1.2field-weighted citation impact, top 24% 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, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Molecular mechanism underlying juvenile hormone-mediated repression of precocious larval-adult metamorphosis.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  8. Article
  9. Sexual transfer of the steroid hormone 20E induces the postmating switch in Anopheles gambiae.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  10. 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 3 institutions in 1 country.

Manabu KamimuraNational Institute of Agrobiological Sciences, Owashi, Tsukuba, Ibaraki 305-8634, Japan. kamimura@affrc.go.jp
Hitoshi Saito
Ryusuke Niwa
Teruyuki Niimi
Kinuko Toyoda
Chihiro Ueno
Yasushi Kanamori
Sachiko Shimura
Makoto Kiuchi
Institute of Agrobiological Sciences · JPNagoya University · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Steroid hormones ecdysteroids regulate varieties of developmental processes in insects. Although the ecdysteroid titer can be increased experimentally with ease, its artificial reduction, although desirable, is very difficult to achieve. Here we characterized the ecdysteroid-inactivating enzyme ecdysteroid-22-oxidase (E22O) from the entomopathogenic fungus Nomuraea rileyi and used it to develop methods for reducing ecdysteroid titer and thereby controlling insect development. K(m) and K(cat) values of the purified E22O for oxidizing ecdysone were 4.4 μM and 8.4/s, respectively, indicating that E22O can inactivate ecdysone more efficiently than other ecdysteroid inactivating enzymes characterized so far. The cloned E22O cDNA encoded a FAD-dependent oxidoreductase. Injection of recombinant E22O into the silkworm Bombyx mori interfered with larval molting and metamorphosis. In the hemolymph of E22O-injected pupae, the titer of hormonally active 20-hydroxyecdysone decreased and concomitantly large amounts of inactive 22-dehydroecdysteroids accumulated. E22O injection also prevented molting of various other insects. In the larvae of the crambid moth Haritalodes basipunctalis, E22O injection induced a diapause-like developmental arrest, which, as in normal diapause, was broken by chilling. Transient expression of the E22O gene by in vivo lipofection effectively decreased the 20-hydroxyecdysone titer and blocked molting in B. mori. Transgenic expression of E22O in Drosophila melanogaster caused embryonic morphological defects, phenotypes of which were very similar to those of the ecdysteroid synthesis deficient mutants. Thus, as the first available simple but versatile tool for reducing the internal ecdysteroid titer, E22O could find use in controlling a broad range of ecdysteroid-associated developmental and physiological phenomena.

Indexed as

MoltingAnimalsAscomycotaBase SequenceBombyxDrosophila melanogasterEcdysteroidsFungal ProteinsLarvaMolecular Sequence DataOxidation-ReductionOxidoreductasesEcdysteroidsFungal ProteinsOxidoreductases

Identifiers

PMID22427652
PMCPMC3351327
OpenAlexW2039433425

What OpenQuestion holds

Textmetadata
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.