Evidence map›Paper›PMID 21190724›Full record

ArticleJournal of human evolution2011

Comparative expression analysis of the phosphocreatine circuit in extant primates: Implications for human brain evolution.

Adam D Pfefferle, Lisa R Warner, Catrina W Wang, William J Nielsen, Courtney C Babbitt, Olivier Fedrigo, Gregory A Wray

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of human evolution, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  10. 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
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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

7 authors at 1 institution in 1 country.

Adam D Pfefferle *Biology Department, Duke University, Durham, USA.
Lisa R Warner *Biology Department, Duke University, Durham, USA.
Catrina W WangBiology Department, Duke University, Durham, USA.
William J NielsenBiology Department, Duke University, Durham, USA.
Courtney C BabbittBiology Department, Duke University, Durham, USA.
Olivier FedrigoBiology Department, Duke University, Durham, USA.
Gregory A WrayBiology Department, Duke University, Durham, USA.
Duke University · US

Funding

ZETA CHAIN OF T CELL RECEPTOR INTERACTS W/ NEF OF SIV &HIV2P51RR000168 · NCRR · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WESTMORELAND, SUSAN V. · 1985 to 2011
$139.3M
The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
WNV REPLIVAX VACCINE IN NON-HUMAN PRIMATESP51RR013986 · NCRR · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI GAUDUIN, MARIE-CLAIRE ELISABETH · 1999 to 2011
$79.1M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
MOUSE MODELS OF CANCER, BONE DISEASE, AND LACTATIONK26RR000168 · NCRR · OHIO STATE UNIVERSITY · PI ROSOL, THOMAS J · 2000 to 2004
$547k
NCRR NIH HHS K26 RR000168NCRR NIH HHS P51 RR000165NCRR NIH HHS P51 RR000168NCRR NIH HHS P51 RR013986NCRR NIH HHS RR000165NCRR NIH HHS RR00168NIAID NIH HHS UC6 AI058607NIAID NIH HHS UC6-AI058607NIH HHS P51 OD011133
6 · The paper itself

Abstract

While the hominid fossil record clearly shows that brain size has rapidly expanded over the last ~2.5 M.yr. the forces driving this change remain unclear. One popular hypothesis proposes that metabolic adaptations in response to dietary shifts supported greater encephalization in humans. An increase in meat consumption distinguishes the human diet from that of other great apes. Creatine, an essential metabolite for energy homeostasis in muscle and brain tissue, is abundant in meat and was likely ingested in higher quantities during human origins. Five phosphocreatine circuit proteins help regulate creatine utilization within energy demanding cells. We compared the expression of all five phosphocreatine circuit genes in cerebral cortex, cerebellum, and skeletal muscle tissue for humans, chimpanzees, and rhesus macaques. Strikingly, SLC6A8 and CKB transcript levels are higher in the human brain, which should increase energy availability and turnover compared to non-human primates. Combined with other well-documented differences between humans and non-human primates, this allocation of energy to the cerebral cortex and cerebellum may be important in supporting the increased metabolic demands of the human brain.

Indexed as

Biological EvolutionAnimalsBrainCreatine Kinase, BB FormCreatine Kinase, Mitochondrial FormCreatine Kinase, MM FormHumansMacaca mulattaMembrane Transport ProteinsMuscle, SkeletalPan troglodytesPhosphocreatinePrimatesCreatine Kinase, BB FormCreatine Kinase, Mitochondrial FormCreatine Kinase, MM Formcreatine transporterMembrane Transport ProteinsPhosphocreatine

Identifiers

PMID21190724
PMCPMC4136512
OpenAlexW2123830045

What OpenQuestion holds

Textmetadata
LicenceTDM
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.