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New markers for regulation of transcription and macromolecule metabolic process in porcine oocytes during in vitro maturation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F20%3A00116243" target="_blank" >RIV/00216224:14110/20:00116243 - isvavai.cz</a>

  • Alternative codes found

    RIV/65269705:_____/20:00072696

  • Result on the web

    <a href="https://www.spandidos-publications.com/10.3892/mmr.2020.10963" target="_blank" >https://www.spandidos-publications.com/10.3892/mmr.2020.10963</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3892/mmr.2020.10963" target="_blank" >10.3892/mmr.2020.10963</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    New markers for regulation of transcription and macromolecule metabolic process in porcine oocytes during in vitro maturation

  • Original language description

    Oocyte maturation is essential for proper fertilization, embryo implantation and early development. While the physiological conditions of these processes are relatively well-known, its exact molecular mechanisms remain widely undiscovered. Oocyte growth, differentiation and maturation are therefore the subject of scientific debate. Precious literature has indicated that the oocyte itself serves a regulatory role in the mechanisms underlying these processes. Hence, the present study performed expression microarrays to analyze the complete transcriptome of porcine oocytes during their in vitro maturation (IVM). Pig material was used for experimentation, as it possesses similarities to the reproductive processes and general genetic proximities of Sus scrofa to human. Oocytes, isolated from the ovaries of slaughtered animals were assessed via the Brilliant Cresyl Blue test and directed to IVM. A number of oocytes were left to be analyzed as the 'before IVM' group. Oocyte mRNA was isolated and used for microarray analysis, which was subsequently validated via RT-qPCR. The current study particularly focused on genes belonging to 'positive regulation of transcription, DNA-dependent', 'positive regulation of gene expression', 'positive regulation of macromolecule metabolic process' and 'positive regulation of transcription from RNA polymerase II promoter' ontologies. FOS, VEGFA, ESR1, AR, CCND2, EGR2, ENDRA, GJA1, INHBA, IHH, INSR, APP, WWTR1, SMARCA1, NFAT5, SMAD4, MAP3K1, EGR1, RORA, ECE1, NR5A1, KIT, IKZF2, MEF2C, SH3D19, MITF and PSMB4 were all determined to be significantly altered (fold change, &gt;|2|; P&lt;0.05) among these groups, with their downregulation being observed after IVM. Genes with the most altered expressions were analyzed and considered to be potential markers of maturation associated with transcription regulation and macromolecule metabolism process.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10601 - Cell biology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Molecular Medicine Reports

  • ISSN

    1791-2997

  • e-ISSN

    1791-3004

  • Volume of the periodical

    21

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    GR - GREECE

  • Number of pages

    15

  • Pages from-to

    1537-1551

  • UT code for WoS article

    000515676300061

  • EID of the result in the Scopus database

    2-s2.0-85078719696