Evidence map›Paper›PMID 26735517›Full record

ArticlePloS one2016

The Swine Plasma Metabolome Chronicles "Many Days" Biological Timing and Functions Linked to Growth.

Timothy G Bromage, Youssef Idaghdour, Rodrigo S Lacruz, Thomas D Crenshaw, Olexandra Ovsiy, Björn Rotter, Klaus Hoffmeier, Friedemann Schrenk

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  17. The biorhythm of human skeletal growth.Journal of anatomy · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Timothy G BromageDepartment of Biomaterials & Biomimetics, New York University College of Dentistry, New York, New York, United States of America.
Youssef IdaghdourDepartment of Biology, New York University Abu Dhabi, Abu Dhabi, United Arab Emirates.
Rodrigo S LacruzDepartment of Basic Science & Craniofacial Biology, New York University College of Dentistry, New York, New York, United States of America.
Thomas D CrenshawDepartment of Animal Science, University of Wisconsin, Madison, Wisconsin, United States of America.
Olexandra OvsiyDepartment of Biomaterials & Biomimetics, New York University College of Dentistry, New York, New York, United States of America.
Björn RotterGenXPro GmbH, Frankfurt am Main, Germany.
Klaus HoffmeierGenXPro GmbH, Frankfurt am Main, Germany.
Friedemann SchrenkDepartment of Palaeoanthropology, Senckenberg Research Institute, Frankfurt am Main, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The paradigm of chronobiology is based almost wholly upon the daily biological clock, or circadian rhythm, which has been the focus of intense molecular, cellular, pharmacological, and behavioral, research. However, the circadian rhythm does not explain biological timings related to fundamental aspects of life history such as rates of tissue/organ/body size development and control of the timing of life stages such as gestation length, age at maturity, and lifespan. This suggests that another biological timing mechanism is at work. Here we focus on a "many days" (multidien) chronobiological period first observed as enigmatic recurring growth lines in developing mammalian tooth enamel that is strongly associate with all adult tissue, organ, and body masses as well as life history attributes such as gestation length, age at maturity, weaning, and lifespan, particularly among the well studied primates. Yet, knowledge of the biological factors regulating the patterning of mammalian life, such as the development of body size and life history structure, does not exist. To identify underlying molecular mechanisms we performed metabolome and genome analyses from blood plasma in domestic pigs. We show that blood plasma metabolites and small non-coding RNA (sncRNA) drawn from 33 domestic pigs over a two-week period strongly oscillate on a 5-day multidien rhythm, as does the pig enamel rhythm. Metabolomics and genomics pathway analyses actually reveal two 5-day rhythms, one related to growth in which biological functions include cell proliferation, apoptosis, and transcription regulation/protein synthesis, and another 5-day rhythm related to degradative pathways that follows three days later. Our results provide experimental confirmation of a 5-day multidien rhythm in the domestic pig linking the periodic growth of enamel with oscillations of the metabolome and genome. This association reveals a new class of chronobiological rhythm and a snapshot of the biological bases that regulate mammalian growth, body size, and life history.

Indexed as

MetabolomeAnimalsBiological ClocksCircadian RhythmDental EnamelFemaleGenomicsMetabolomicsRNA, UntranslatedSwineRNA, Untranslated

Identifiers

PMID26735517
PMCPMC4703299

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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.