Evidence map›Paper›PMID 25409740›Full record

ArticleBMC genomics2014

Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes.

Maria B Rabaglino, Maureen Keller-Wood, Charles E Wood

Abstract read
In one paragraph

Article in BMC genomics, 2014. 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
–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

11 citing papers in PubMed.

  1. Article
  2. Epigenomic and transcriptomic analyses reveal early activation of the HPG axis in in vitro-produced male dairy calves.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  3. Article
  4. Current paradigms and new perspectives on fetal hypoxia: implications for fetal brain development in late gestation.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. A question of cytokine signaling in the fetus.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2015
    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

3 authors.

Maria B RabaglinoDepartamento de Reproducción Animal, Fac, Agronomía y Veterinaria, Universidad Nacional de Río Cuarto, Córdoba, Argentina. brabaglino@ufl.edu.
Maureen Keller-Wood
Charles E Wood

Funding

FETAL REFLEX RESPONSES TO CEREBRAL HYPOPERFUSIONR01HD033053 · NICHD · UNIVERSITY OF FLORIDA · PI WOOD, CHARLES E · 1996 to 2016
$4.1M
Estrogen Influences on Fetal AdrenocorticotropinR01HD042135 · NICHD · UNIVERSITY OF FLORIDA · PI WOOD, CHARLES E · 2002 to 2006
$1.4M
Research Career Development in Child HealthK12HD057581 · NICHD · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2008 to 2012
$1.4M
Renal Transporters and Fetal NeuroendocrinologyR01HD057561 · NICHD · UNIVERSITY OF FLORIDA · PI WOOD, CHARLES E · 2009 to 2013
$1.4M
NICHD NIH HHS HD033053NICHD NIH HHS HD057561NICHD NIH HHS HD057581NICHD NIH HHS K12 HD057581NICHD NIH HHS R01 HD033053NICHD NIH HHS R01 HD042135NICHD NIH HHS R01 HD057561
6 · The paper itself

Abstract

backgroundMajor changes in gene expression occur in the fetal brain to modulate the function of this organ postnatally. Thus, factors can alter the genomics of the fetal brain, predisposing to neurological disorders later in life. We hypothesized that the physiological dynamics of the immune system transcriptome of the fetal brain during the last stage of gestation will reveal patterns of immune function and development in the developing brain. In this study we applied weighted gene co-expression analysis of microarrays performed on ovine fetal brain samples, to model the changes in gene expression throughout the second half of gestation.

resultsClusters of co-expressed genes that strongly increase in expression toward the first day of extra-uterine life are related to the hematopoietic lineage, while activation of immune pathways is induced after birth. Moreover, the pattern of gene expression suggests induction of tolerance mechanisms, probably necessary to protect highly produced proteins--such as myelin basic protein--from an autoimmune attack.

conclusionsThis study provides insight into the dramatic changes in gene expression that take place in the brain during the fetal life, especially during the last stage of gestation, and suggests that the immune system may have an important role in maturation of the fetal brain, which if disrupted or altered, could have negative consequences in postnatal life.

Indexed as

Gene Expression Regulation, DevelopmentalModels, BiologicalAnimalsBiomarkersBrainFemaleFetusGene Expression ProfilingGene Regulatory NetworksHematopoiesisPregnancyReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionSheepBiomarkers

Identifiers

PMID25409740
PMCPMC4253626

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Registered trials

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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.