Genes regulating hormone stimulus and response to protein signaling revealed differential expression pattern during porcine oocyte in vitro maturation, confirmed by lipid concentration

Authors

CHERMULA Blazej JEŠETA Michal SUJKA-KORDOWSKA Patrycja KONWERSKA Aneta JANKOWSKI Maurycy KRANC Wieslawa KOCHEROVA Ievgeniia CELICHOWSKI Piotr ANTOSIK Piotr BUKOWSKA Dorota MILAKOVIC Irena MACHATKOVA Marie PAWELCZYK Leszek IZYCKI Dariusz ZABEL Maciej MOZDZIAK Paul KEMPISTY Bartosz PIOTROWSKA-KEMPISTY Hanna

Year of publication 2020
Type Article in Periodical
Magazine / Source Histochemistry and Cell Biology
MU Faculty or unit

Faculty of Medicine

Citation
Web https://link.springer.com/article/10.1007/s00418-020-01866-w
Doi http://dx.doi.org/10.1007/s00418-020-01866-w
Keywords Pig; Oocyte maturation; Microarray; Mitochondrial activity
Description Genes influencing oocyte maturation may be valuable for predicting their developmental potential, as well as discerning the mechanistic pathways regulating oocyte development. In the presented research microarray gene expression analysis of immature and in vitro matured porcine oocytes was performed. Two groups of oocytes were compared in the study: before (3 x n = 50) and after in vitro maturation (3 x n = 50). The selection of viable oocytes was performed using the brilliant cresyl blue (BCB) test. Furthermore, microarrays and RT-qPCR was used to analyze the transcriptome of the oocytes before and after IVM. The study focused on the genes undergoing differential expression in two gene-ontology groups: "Cellular response to hormone stimulus" and "Cellular response to unfolded protein", which contain genes that may directly or indirectly be involved in signal transduction during oocyte maturation. Examination of all the genes of interest showed a lower level of their expression after IVM. From the total number of genes in these gene ontologies ten of the highest change in expression were identified: FOS, ID2, BTG2, CYR61, ESR1, AR, TACR3, CCND2, EGR2 and TGFBR3. The successful maturation of the oocytes was additionally confirmed with the use of lipid droplet assay. The genes were briefly described and related to the literature sources, to investigate their potential roles in the process of oocyte maturation. The results of the study may serve as a basic molecular reference for further research aimed at improving the methods of oocyte in vitro maturation, which plays an important role in the procedures of assisted reproduction.

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