Evidence map›Paper›PMID 33990225›Full record

ArticleEvoDevo2021

Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster.

Jeanne M C McDonald, Pegah Nabili, Lily Thorsen, Sohee Jeon, Alexander W Shingleton

Open access · goldAbstract read
In one paragraph

Article in EvoDevo, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 24 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

5 authors at 2 institutions in 1 country.

Jeanne M C McDonald *Department of Ecology and Evolutionary Biology, Cornell University, Corson Hall Ithaca, NY, 14853, USA.
Pegah Nabili *Department of Biology, Lake Forest College, 555 North Sheridan Road, Lake Forest, IL, 60045, USA.
Lily Thorsen *Department of Biology, Lake Forest College, 555 North Sheridan Road, Lake Forest, IL, 60045, USA.
Sohee JeonDepartment of Biological Sciences, University of Illinois at Chicago, 840 W Taylor Street, Chicago, IL, 60607, USA.
Alexander W ShingletonDepartment of Biology, Lake Forest College, 555 North Sheridan Road, Lake Forest, IL, 60045, USA. ashingle@uic.edu.ORCID http://orcid.org/0000-0001-9862-9947
Lake Forest College · USUniversity of Illinois Chicago · US

Funding

Division of Integrative Organismal Systems 1952385
6 · The paper itself

Abstract

backgroundSexual-size dimorphism (SSD) is replete among animals, but while the selective pressures that drive the evolution of SSD have been well studied, the developmental mechanisms upon which these pressures act are poorly understood. Ours and others' research has shown that SSD in D. melanogaster reflects elevated levels of nutritional plasticity in females versus males, such that SSD increases with dietary intake and body size, a phenomenon called sex-specific plasticity (SSP). Additional data indicate that while body size in both sexes responds to variation in protein level, only female body size is sensitive to variation in carbohydrate level. Here, we explore whether these difference in sensitivity at the morphological level are reflected by differences in how the insulin/IGF-signaling (IIS) and TOR-signaling pathways respond to changes in carbohydrates and proteins in females versus males, using a nutritional geometry approach.

resultsThe IIS-regulated transcripts of 4E-BP and InR most strongly correlated with body size in females and males, respectively, but neither responded to carbohydrate level and so could not explain the sex-specific response to body size to dietary carbohydrate. Transcripts regulated by TOR-signaling did, however, respond to dietary carbohydrate in a sex-specific manner. In females, expression of dILP5 positively correlated with body size, while expression of dILP2,3 and 8, was elevated on diets with a low concentration of both carbohydrate and protein. In contrast, we detected lower levels of dILP2 and 5 protein in the brains of females fed on low concentration diets. We could not detect any effect of diet on dILP expression in males.

conclusionAlthough females and males show sex-specific transcriptional responses to changes in protein and carbohydrate, the patterns of expression do not support a simple model of the regulation of body-size SSP by either insulin- or TOR-signaling. The data also indicate a complex relationship between carbohydrate and protein level, dILP expression and dILP peptide levels in the brain. In general, diet quality and sex both affect the transcriptional response to changes in diet quantity, and so should be considered in future studies that explore the effect of nutrition on body size.

Indexed as

Body sizeInsulin/IGF-signalingNutritionSex-specific plasticitySexual-size dimorphismTOR-signaling

Identifiers

PMID33990225
PMCPMC8120840
OpenAlexW2776053860

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.