• Something wrong with this record ?

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

B. Chermuła, M. Jeseta, P. Sujka-Kordowska, A. Konwerska, M. Jankowski, W. Kranc, I. Kocherova, P. Celichowski, P. Antosik, D. Bukowska, I. Milakovic, M. Machatkova, L. Pawelczyk, D. Iżycki, M. Zabel, P. Mozdziak, B. Kempisty, H. Piotrowska-Kempisty,

. 2020 ; 154 (1) : 77-95. [pub] 20200318

Language English Country Germany

Document type Journal Article

Grant support
FNBr, 65269705 Ministry of Health, Czech Republic

E-resources Online Full text

NLK ProQuest Central from 1997-01-01 to 1 year ago
Medline Complete (EBSCOhost) from 2000-01-01 to 1 year ago
Nursing & Allied Health Database (ProQuest) from 1997-01-01 to 1 year ago
Health & Medicine (ProQuest) from 1997-01-01 to 1 year ago
Public Health Database (ProQuest) from 1997-01-01 to 1 year ago

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 × n = 50) and after in vitro maturation (3 × 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.

Chair of Biotechnology Department of Cancer Immunology Poznan University of Medical Sciences Poznan Poland

Department of Anatomy Poznan University of Medical Sciences Poznan Poland

Department of Elementary and Preclinical Sciences Nicolaus Copernicus University in Torun Toruń Poland

Department of Histology and Embryology Poznan University of Medical Sciences 6 Święcickiego St 60 781 Poznan Poland

Department of Histology and Embryology Wroclaw Medical University Wrocław Poland Division of Anatomy and Histology University of Zielona Gora Zielona Gora Poland

Department of Obstetrics and Gynecology University Hospital and Masaryk University Brno Czech Republic

Department of Obstetrics and Gynecology University Hospital and Masaryk University Brno Czech Republic Department of Histology and Embryology Poznan University of Medical Sciences 6 Święcickiego St 60 781 Poznan Poland Department of Anatomy Poznan University of Medical Sciences Poznan Poland Department of Veterinary Surgery Nicolaus Copernicus University in Torun Toruń Poland

Department of Toxicology Poznan University of Medical Sciences Poznan Poland

Department of Veterinary Surgery Nicolaus Copernicus University in Torun Toruń Poland

Division of Infertility and Reproductive Endocrinology Department of Gynecology Obstetrics and Gynecological Oncology Poznan University of Medical Sciences Poznan Poland

Physiology Graduate Program North Carolina State University Raleigh NC USA

Veterinary Research Institute Brno Czech Republic

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc20028053
003      
CZ-PrNML
005      
20210114152901.0
007      
ta
008      
210105s2020 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00418-020-01866-w $2 doi
035    __
$a (PubMed)32189110
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Chermuła, Błażej $u Division of Infertility and Reproductive Endocrinology, Department of Gynecology, Obstetrics and Gynecological Oncology, Poznan University of Medical Sciences, Poznan, Poland.
245    10
$a Genes regulating hormone stimulus and response to protein signaling revealed differential expression pattern during porcine oocyte in vitro maturation, confirmed by lipid concentration / $c B. Chermuła, M. Jeseta, P. Sujka-Kordowska, A. Konwerska, M. Jankowski, W. Kranc, I. Kocherova, P. Celichowski, P. Antosik, D. Bukowska, I. Milakovic, M. Machatkova, L. Pawelczyk, D. Iżycki, M. Zabel, P. Mozdziak, B. Kempisty, H. Piotrowska-Kempisty,
520    9_
$a 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 × n = 50) and after in vitro maturation (3 × 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.
650    _2
$a zvířata $7 D000818
650    _2
$a kultivované buňky $7 D002478
650    _2
$a eosin $x chemie $7 D004801
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a hematoxylin $x chemie $7 D006416
650    _2
$a hormony $x genetika $x metabolismus $7 D006728
650    12
$a IVM techniky $7 D059471
650    _2
$a lipidy $x analýza $7 D008055
650    _2
$a oocyty $x růst a vývoj $x metabolismus $7 D009865
650    _2
$a oxaziny $x chemie $7 D010078
650    _2
$a signální transdukce $7 D015398
650    _2
$a prasata $7 D013552
655    _2
$a časopisecké články $7 D016428
700    1_
$a Jeseta, Michal $u Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Brno, Czech Republic.
700    1_
$a Sujka-Kordowska, Patrycja $u Department of Histology and Embryology, Poznan University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland.
700    1_
$a Konwerska, Aneta $u Department of Histology and Embryology, Poznan University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland.
700    1_
$a Jankowski, Maurycy $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
700    1_
$a Kranc, Wiesława $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
700    1_
$a Kocherova, Ievgeniia $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
700    1_
$a Celichowski, Piotr $u Department of Histology and Embryology, Poznan University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland.
700    1_
$a Antosik, Paweł $u Department of Veterinary Surgery, Nicolaus Copernicus University in Torun, Toruń, Poland.
700    1_
$a Bukowska, Dorota $u Department of Elementary and Preclinical Sciences, Nicolaus Copernicus University in Torun, Toruń, Poland.
700    1_
$a Milakovic, Irena $u Veterinary Research Institute, Brno, Czech Republic.
700    1_
$a Machatkova, Marie $u Veterinary Research Institute, Brno, Czech Republic.
700    1_
$a Pawelczyk, Leszek $u Division of Infertility and Reproductive Endocrinology, Department of Gynecology, Obstetrics and Gynecological Oncology, Poznan University of Medical Sciences, Poznan, Poland.
700    1_
$a Iżycki, Dariusz $u Chair of Biotechnology, Department of Cancer Immunology, Poznan University of Medical Sciences, Poznan, Poland.
700    1_
$a Zabel, Maciej $u Department of Histology and Embryology, Wroclaw Medical University, Wrocław, Poland. Division of Anatomy and Histology, University of Zielona Gora, Zielona Gora, Poland.
700    1_
$a Mozdziak, Paul $u Physiology Graduate Program, North Carolina State University, Raleigh, NC, USA.
700    1_
$a Kempisty, Bartosz $u Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Brno, Czech Republic. bkempisty@ump.edu.pl. Department of Histology and Embryology, Poznan University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland. bkempisty@ump.edu.pl. Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland. bkempisty@ump.edu.pl. Department of Veterinary Surgery, Nicolaus Copernicus University in Torun, Toruń, Poland. bkempisty@ump.edu.pl.
700    1_
$a Piotrowska-Kempisty, Hanna $u Department of Toxicology, Poznan University of Medical Sciences, Poznan, Poland.
773    0_
$w MED00002042 $t Histochemistry and cell biology $x 1432-119X $g Roč. 154, č. 1 (2020), s. 77-95
856    41
$u https://pubmed.ncbi.nlm.nih.gov/32189110 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20210105 $b ABA008
991    __
$a 20210114152858 $b ABA008
999    __
$a ok $b bmc $g 1608388 $s 1119233
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 154 $c 1 $d 77-95 $e 20200318 $i 1432-119X $m Histochemistry and cell biology $n Histochem Cell Biol $x MED00002042
GRA    __
$a FNBr, 65269705 $p Ministry of Health, Czech Republic
LZP    __
$a Pubmed-20210105

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...