Evidence map›Paper›PMID 21986508›Full record

ArticleBrain, behavior and evolution2011

A potential role for glucose transporters in the evolution of human brain size.

Olivier Fedrigo, Adam D Pfefferle, Courtney C Babbitt, Ralph Haygood, Christine E Wall, Gregory A Wray

Open access · bronzeAbstract read
In one paragraph

Article in Brain, behavior and evolution, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. A Role for Astrocyte Metabolism in Species-Specific Neuronal Development.bioRxiv : the preprint server for biology · 2026
    Article
  2. Primate gut microbiota induce evolutionarily salient changes in mouse neurodevelopment.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  15. Metabolic constraint imposes tradeoff between body size and number of brain neurons in human evolution.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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

6 authors at 1 institution in 1 country.

Olivier FedrigoBiology Department, Duke University, Durham, NC, USA. ofedrigo@duke.edu
Adam D Pfefferle
Courtney C Babbitt
Ralph Haygood
Christine E Wall
Gregory A Wray
Duke University · US

Funding

Project 6P50GM081883 · NIGMS · DUKE UNIVERSITY · PI BENFEY, PHILIP N · 2007 to 2012
$14.9M
NIGMS NIH HHS 5P50-GM-081883-02NIGMS NIH HHS P50 GM081883
6 · The paper itself

Abstract

Differences in cognitive abilities and the relatively large brain are among the most striking differences between humans and their closest primate relatives. The energy trade-off hypothesis predicts that a major shift in energy allocation among tissues occurred during human origins in order to support the remarkable expansion of a metabolically expensive brain. However, the molecular basis of this adaptive scenario is unknown. Two glucose transporters (SLC2A1 and SLC2A4) are promising candidates and present intriguing mutations in humans, resulting, respectively, in microcephaly and disruptions in whole-body glucose homeostasis. We compared SLC2A1 and SLC2A4 expression between humans, chimpanzees and macaques, and found compensatory and biologically significant expression changes on the human lineage within cerebral cortex and skeletal muscle, consistent with mediating an energy trade-off. We also show that these two genes are likely to have undergone adaptation and participated in the development and maintenance of a larger brain in the human lineage by modulating brain and skeletal muscle energy allocation. We found that these two genes show human-specific signatures of positive selection on known regulatory elements within their 5'-untranslated region, suggesting an adaptation of their regulation during human origins. This study represents the first case where adaptive, functional and genetic lines of evidence implicate specific genes in the evolution of human brain size.

Indexed as

Biological EvolutionAnimalsBase SequenceBrainGene ExpressionGlucose Transporter Type 4HumansMacacaMolecular Sequence DataOrgan SizePan troglodytesReal-Time Polymerase Chain ReactionSodium-Phosphate Cotransporter Proteins, Type IIISpecies SpecificityGlucose Transporter Type 4SLC20A1 protein, humanSLC2A4 protein, humanSodium-Phosphate Cotransporter Proteins, Type III

Identifiers

PMID21986508
PMCPMC3237107
OpenAlexW1530291120

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.