Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

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

J. Budna, M. Rybska, S. Ciesiółka, A. Bryja, S. Borys, W. Kranc, K. Wojtanowicz-Markiewicz, M. Jeseta, E. Sumelka, D. Bukowska, P. Antosik, KP. Brüssow, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,

. 2017 ; 15 (1) : 43. [pub] 20170602

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18010521

BACKGROUND: The 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. METHODS: Oocytes 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. RESULTS: The 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). CONCLUSIONS: Increased 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.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18010521
003      
CZ-PrNML
005      
20180418125432.0
007      
ta
008      
180404s2017 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.1186/s12958-017-0261-6 $2 doi
035    __
$a (PubMed)28576120
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Budna, Joanna $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
245    10
$a Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM - a microarray approach / $c J. Budna, M. Rybska, S. Ciesiółka, A. Bryja, S. Borys, W. Kranc, K. Wojtanowicz-Markiewicz, M. Jeseta, E. Sumelka, D. Bukowska, P. Antosik, KP. Brüssow, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,
520    9_
$a BACKGROUND: The 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. METHODS: Oocytes 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. RESULTS: The 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). CONCLUSIONS: Increased 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.
650    _2
$a zvířata $7 D000818
650    _2
$a kostní morfogenetické proteiny $x genetika $x metabolismus $7 D019485
650    _2
$a kumulární buňky $x cytologie $x metabolismus $x fyziologie $7 D054885
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a stanovení celkové genové exprese $7 D020869
650    _2
$a vývojová regulace genové exprese $7 D018507
650    12
$a IVM techniky $7 D059471
650    _2
$a mikročipová analýza $7 D046228
650    _2
$a oocyty $x cytologie $x metabolismus $x fyziologie $7 D009865
650    _2
$a oogeneze $x genetika $7 D009866
650    _2
$a signální transdukce $x genetika $7 D015398
650    _2
$a prasata $x genetika $x metabolismus $7 D013552
650    _2
$a transkriptom $7 D059467
655    _2
$a časopisecké články $7 D016428
700    1_
$a Rybska, Marta $u Institute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
700    1_
$a Ciesiółka, Sylwia $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
700    1_
$a Bryja, Artur $u Department of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
700    1_
$a Borys, Sylwia $u Department of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
700    1_
$a Kranc, Wiesława $u Department of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
700    1_
$a Wojtanowicz-Markiewicz, Katarzyna $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland. Institute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
700    1_
$a Jeseta, Michal $u Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Obilnitrh 11, 602 00, Brno, Czech Republic.
700    1_
$a Sumelka, Ewa $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
700    1_
$a Bukowska, Dorota $u Institute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
700    1_
$a Antosik, Paweł $u Institute of Veterinary Sciences, Poznan University of Life Sciences, Wolynska 35 St, 60-637, Poznan, Poland.
700    1_
$a Brüssow, Klaus P $u Department of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
700    1_
$a Bruska, Małgorzata $u Department of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland.
700    1_
$a Nowicki, Michał $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
700    1_
$a Zabel, Maciej $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
700    1_
$a Kempisty, Bartosz $u Department of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland. bkempisty@ump.edu.pl. Department of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St, 60-781, Poznan, Poland. bkempisty@ump.edu.pl.
773    0_
$w MED00008251 $t Reproductive biology and endocrinology RB&E $x 1477-7827 $g Roč. 15, č. 1 (2017), s. 43
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28576120 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180404 $b ABA008
991    __
$a 20180418125531 $b ABA008
999    __
$a ok $b bmc $g 1288006 $s 1007333
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 15 $c 1 $d 43 $e 20170602 $i 1477-7827 $m Reproductive biology and endocrinology $n Reprod Biol Endocrinol $x MED00008251
LZP    __
$a Pubmed-20180404

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...