Evidence map›Paper›PMID 28576120›Full record

ArticleReproductive biology and endocrinology : RB&E2017

Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM - a microarray approach.

Joanna Budna, Marta Rybska, Sylwia Ciesiółka, Artur Bryja, Sylwia Borys, Wiesława Kranc, Katarzyna Wojtanowicz-Markiewicz, Michal Jeseta, Ewa Sumelka, Dorota Bukowska and 6 more

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 15 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

16 authors at 3 institutions in 2 countries.

Joanna BudnaDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Marta RybskaInstitute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
Sylwia CiesiółkaDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Artur BryjaDepartment of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
Sylwia BorysDepartment of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
Wiesława KrancDepartment of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
Katarzyna Wojtanowicz-MarkiewiczDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Michal JesetaDepartment of Obstetrics and Gynecology, University Hospital and Masaryk University, Obilnitrh 11, 602 00, Brno, Czech Republic.
Ewa SumelkaDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Dorota BukowskaInstitute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
Paweł AntosikInstitute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
Klaus P BrüssowDepartment of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
Małgorzata BruskaDepartment of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
Michał NowickiDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Maciej ZabelDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Bartosz KempistyDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland. bkempisty@ump.edu.pl.
Poznan University of Medical Sciences · PLUniversity of Life Sciences in Poznań · PLMasaryk University · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe full maturational capability of mammalian oocytes is accompanied by nuclear and cytoplasmic modifications, which are associated with proliferation and differentiation of surrounding cumulus cells. These events are regulated on molecular level by the expression of target genes involved in signal transduction pathways crucial for folliculogenesis and oogenesis. Transforming growth factor beta signaling includes several molecules that are involved in the regulation of oogenesis and embryo growth, including bone morphogenetic protein (BMP). However, the BMP-related gene expression profile in oocytes at different maturational stages requires further investigation.

methodsOocytes were isolated from pubertal crossbred Landrace gilts follicles, selected with a use of BCB staining test and analyzed before and after in vitro maturation. Gene expression profiles were examined using an Affymetrix microarray approach and validated by RT-qPCR. Database for Annotation, Visualization, and Integrated Discovery (DAVID) software was used for the extraction of the genes belonging to a BMP-signaling pathway ontology group.

resultsThe assay revealed 12,258 different transcripts in porcine oocytes, among which 379 genes were down-regulated and 40 were up-regulated. The DAVID database indicated a "BMP signaling pathway" ontology group, which was significantly regulated in both groups of oocytes. We discovered five up-regulated genes in oocytes before versus after in vitro maturation (IVM): chordin-like 1 (CHRDL1), follistatin (FST), transforming growth factor-beta receptor-type III (TGFβR3), decapentaplegic homolog 4 (SMAD4), and inhibitor of DNA binding 1 (ID1).

conclusionsIncreased expression of CHRDL1, FST, TGFβR3, SMAD4, and ID1 transcripts before IVM suggested a subordinate role of the BMP signaling pathway in porcine oocyte maturational competence. Conversely, it is postulated that these genes are involved in early stages of folliculogenesis and oogenesis regulation in pigs, since in oocytes before IVM increased expression was observed.

Indexed as

In Vitro Oocyte Maturation TechniquesAnimalsBone Morphogenetic ProteinsCumulus CellsFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalMicroarray AnalysisOocytesOogenesisSignal TransductionSwineTranscriptomeBone Morphogenetic ProteinsIn vitro maturationMicroarrayOocytesPig

Identifiers

PMID28576120
PMCPMC5457624
OpenAlexW2620696920

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LicenceCC BY
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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.