Evidence map›Paper›PMID 26108483›Full record

ArticleBMC biology2015

The role of juvenile hormone and insulin/TOR signaling in the growth of Manduca sexta.

Nicole E Hatem, Zhou Wang, Keelin B Nave, Takashi Koyama, Yuichiro Suzuki

Abstract read
In one paragraph

Article in BMC biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Functional Study of the Role of theInternational journal of molecular sciences · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Effects of high-fat diet on feeding and performance in the tobacco hornworm, Manduca sexta.Comparative biochemistry and physiology. Part A, Molecular & integrative physiology · 2019
    Article
  12. TOR as a Regulatory Target inFrontiers in physiology · 2019
    Article
  13. Article
  14. Metamorphosis is induced by food absence rather than a critical weight in the solitary bee,Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Nicole E HatemDepartment of Biological Sciences, Wellesley College, 106 Central St., Wellesley, MA, 02481, USA. nhatem@wellesley.edu.
Zhou WangDepartment of Biological Sciences, Wellesley College, 106 Central St., Wellesley, MA, 02481, USA. zwang@wellesley.edu.
Keelin B NaveDepartment of Biological Sciences, Wellesley College, 106 Central St., Wellesley, MA, 02481, USA. knave@wellesley.edu.
Takashi KoyamaDevelopment, Evolution and the Environment Lab, Instituto Gulbenkian de Ciência, 2780-156, Oeiras, Portugal. tkoyama@igc.gulbenkian.pt.
Yuichiro SuzukiDepartment of Biological Sciences, Wellesley College, 106 Central St., Wellesley, MA, 02481, USA. ysuzuki@wellesley.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn many insect species, fitness trade-offs exist between maximizing body size and developmental speed. Understanding how various species evolve different life history strategies requires knowledge of the physiological mechanisms underlying the regulation of body size and developmental timing. Here the roles of juvenile hormone (JH) and insulin/target of rapamycin (TOR) signaling in the regulation of the final body size were examined in the tobacco hornworm, Manduca sexta.

resultsFeeding rapamycin to wild-type larvae decreased the growth rate but did not alter the peak size of the larvae. In contrast, feeding rapamycin to the JH-deficient black mutant larvae caused the larvae to significantly increase the peak size relative to the DMSO-fed control animals by lengthening the terminal growth period. Furthermore, the critical weight was unaltered by feeding rapamycin, indicating that in Manduca, the critical weight is not influenced by insulin/TOR signaling. In addition, post-critical weight starved black mutant Manduca given rapamycin underwent metamorphosis sooner than those that were fed, mimicking the "bail-out mechanism".

conclusionsOur study demonstrates that JH masks the effects of insulin/TOR signaling in the determination of the final body size and that the critical weights in Drosophila and Manduca rely on distinct mechanisms that reflect different life history strategies. Our study also suggests that TOR signaling lengthens the terminal growth period in Manduca as it does in Drosophila, and that JH levels determine the relative contributions of nutrient- and body size-sensing pathways to metamorphic timing.

Indexed as

AnimalsBody SizeInsulinJuvenile HormonesManducaSignal TransductionTOR Serine-Threonine KinasesInsulinJuvenile HormonesTOR Serine-Threonine Kinases

Identifiers

PMID26108483
PMCPMC4499214

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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.