Evidence map›Paper›PMID 25991861›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Rapid molecular evolution across amniotes of the IIS/TOR network.

Suzanne E McGaugh, Anne M Bronikowski, Chih-Horng Kuo, Dawn M Reding, Elizabeth A Addis, Lex E Flagel, Fredric J Janzen, Tonia S Schwartz

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 65 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

8 authors at 5 institutions in 2 countries.

Suzanne E McGaughDepartment of Ecology, Evolution, and Behavior, University of Minnesota, Saint Paul, MN 55108; smcgaugh@umn.edu abroniko@iastate.edu chk@gate.sinica.edu.tw tschwartz@uab.edu.
Anne M BronikowskiDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, IA 50011; smcgaugh@umn.edu abroniko@iastate.edu chk@gate.sinica.edu.tw tschwartz@uab.edu.
Chih-Horng KuoInstitute of Plant and Microbial Biology, Academia Sinica, Taipei 11529, Taiwan; smcgaugh@umn.edu abroniko@iastate.edu chk@gate.sinica.edu.tw tschwartz@uab.edu.
Dawn M RedingDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, IA 50011;
Elizabeth A AddisDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, IA 50011;
Lex E FlagelDepartment of Plant Biology, University of Minnesota, Saint Paul, MN 55108; Monsanto Company, Chesterfield, MO 63017; and.
Fredric J JanzenDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, IA 50011;
Tonia S SchwartzOffice of Energetics, School of Public Health, University of Alabama, Birmingham, AL 35294 smcgaugh@umn.edu abroniko@iastate.edu chk@gate.sinica.edu.tw tschwartz@uab.edu.ORCID http://orcid.org/0000-0002-7712-2810
Iowa State University · USInstitute of Plant and Microbial Biology, Academia Sinica · TWMonsanto (United States) · USUniversity of Alabama · USUniversity of Minnesota · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

The insulin/insulin-like signaling and target of rapamycin (IIS/TOR) network regulates lifespan and reproduction, as well as metabolic diseases, cancer, and aging. Despite its vital role in health, comparative analyses of IIS/TOR have been limited to invertebrates and mammals. We conducted an extensive evolutionary analysis of the IIS/TOR network across 66 amniotes with 18 newly generated transcriptomes from nonavian reptiles and additional available genomes/transcriptomes. We uncovered rapid and extensive molecular evolution between reptiles (including birds) and mammals: (i) the IIS/TOR network, including the critical nodes insulin receptor substrate (IRS) and phosphatidylinositol 3-kinase (PI3K), exhibit divergent evolutionary rates between reptiles and mammals; (ii) compared with a proxy for the rest of the genome, genes of the IIS/TOR extracellular network exhibit exceptionally fast evolutionary rates; and (iii) signatures of positive selection and coevolution of the extracellular network suggest reptile- and mammal-specific interactions between members of the network. In reptiles, positively selected sites cluster on the binding surfaces of insulin-like growth factor 1 (IGF1), IGF1 receptor (IGF1R), and insulin receptor (INSR); whereas in mammals, positively selected sites clustered on the IGF2 binding surface, suggesting that these hormone-receptor binding affinities are targets of positive selection. Further, contrary to reports that IGF2R binds IGF2 only in marsupial and placental mammals, we found positively selected sites clustered on the hormone binding surface of reptile IGF2R that suggest that IGF2R binds to IGF hormones in diverse taxa and may have evolved in reptiles. These data suggest that key IIS/TOR paralogs have sub- or neofunctionalized between mammals and reptiles and that this network may underlie fundamental life history and physiological differences between these amniote sister clades.

Indexed as

Evolution, MolecularGenetic VariationAnimalsBirdsHumansInsulinMammalsMetabolic Networks and PathwaysModels, GeneticReptilesSelection, GeneticSignal TransductionTOR Serine-Threonine KinasesInsulinTOR Serine-Threonine Kinasesinsulin growth factorinsulin signalingmolecular evolutionrapamycin

Identifiers

PMID25991861
PMCPMC4460498
OpenAlexW1573045758

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.