Evidence map›Paper›PMID 26926596›Full record

ArticlePloS one2016

Cyclic AMP Affects Oocyte Maturation and Embryo Development in Prepubertal and Adult Cattle.

Sandra Milena Bernal-Ulloa, Julia Heinzmann, Doris Herrmann, Klaus-Gerd Hadeler, Patrick Aldag, Sylke Winkler, Dorit Pache, Ulrich Baulain, Andrea Lucas-Hahn, Heiner Niemann

Open access · goldAbstract 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. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 46 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

10 authors at 2 institutions in 2 countries.

Sandra Milena Bernal-UlloaInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Julia HeinzmannInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Doris HerrmannInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Klaus-Gerd HadelerInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Patrick AldagInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Sylke WinklerDNA Sequencing Facility, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Dorit PacheDNA Sequencing Facility, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Ulrich BaulainInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Andrea Lucas-HahnInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Heiner NiemannInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institut, Mariensee, Germany.
Friedrich-Loeffler-Institut · DEMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High cAMP levels during in vitro maturation (IVM) have been related to improved blastocyst yields. Here, we employed the cAMP/cGMP modulators, forskolin, IBMX, and cilostamide, during IVM to unravel the role of high cAMP in early embryonic development produced from prepubertal and adult bovine oocytes. Oocytes were collected via transvaginal aspiration and randomly assigned to three experimental groups: TCM24 (24 h IVM/control), cAMP30 (2 h pre-IVM (forskolin-IBMX), 30 h IVM-cilostamide), and DMSO30 (Dimethyl Sulfoxide/vehicle control). After IVM, oocytes were fertilized in vitro and zygotes were cultured in vitro to blastocysts. Meiotic progression, cAMP levels, mRNA abundance of selected genes and DNA methylation were evaluated in oocytes. Blastocysts were used for gene expression or DNA methylation analyses. Blastocysts from the cAMP30 groups were transferred to recipients. The cAMP elevation delayed meiotic progression, but developmental rates were not increased. In immature oocytes, mRNA abundance of PRKACA was higher for cAMP30 protocol and no differences were found for PDE3A, SMAD2, ZAR1, PRDX1 and SLC2A8. EGR1 gene was up-regulated in prepubertal cAMP30 immature oocytes and down-regulated in blastocysts from all in vitro treatments. A similar gene expression profile was observed for DNMT3b, BCL2L1, PRDX1 and SLC2A8 in blastocysts. Satellite DNA methylation profiles were different between prepubertal and adult oocytes and blastocysts derived from the TCM24 and DMSO30 groups. Blastocysts obtained from prepubertal and adult oocytes in the cAMP30 treatment displayed normal methylation profiles and produced offspring. These data indicate that cAMP regulates IVM in prepubertal and adult oocytes in a similar manner, with impact on the establishment of epigenetic marks and acquisition of full developmental competency.

Indexed as

Embryonic DevelopmentPubertyAnimalsBlastocystCattleCell CountCpG IslandsCyclic AMPDNA MethylationFemaleGene Expression Regulation, DevelopmentalMeiosisOocytesRNA, MessengerCyclic AMPRNA, Messenger

Identifiers

PMID26926596
PMCPMC4771806
OpenAlexW2292288293

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.