Proteomic characterization of bovine granulosa cells in dominant and subordinate follicles.


Journal

Hereditas
ISSN: 1601-5223
Titre abrégé: Hereditas
Pays: England
ID NLM: 0374654

Informations de publication

Date de publication:
2019
Historique:
received: 07 03 2019
accepted: 14 06 2019
entrez: 12 7 2019
pubmed: 12 7 2019
medline: 6 2 2020
Statut: epublish

Résumé

Characterization of molecular factors regulating ovarian follicular development is critical to understanding its functional mechanism of controlling the estrous cycle, determining oocyte competency, and regulating ovulation. In previous studies, we performed next-gene sequencing to investigate the differentially expressed transcripts of bovine follicular granulosa cells (GCs) at the dominant follicle (DF) and subordinate follicle (SF) stages during the first follicular wave. This study aims to investigate the proteomic characterization of GCs of DF and SF in the bovine estrous cycle. In total, 3409 proteins were identified from 30,321 peptides obtained from liquid chromatograph-mass spectrometer analysis. Two hundred fifty-nine of these proteins were found to be expressed differently in DF and SF. Out of 259, a total of 26 proteins were upregulated (fold change≥2) and 233 proteins were downregulated (fold change≤0.5) in DF. Gene Ontology (GO) analysis of proteome data revealed the biological process, cellular component and molecular function of expressed proteins in DF and SF, while the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed important signaling pathways associated with follicular development such as the PI3K-Akt, estrogen, and insulin signaling pathways. Immunoblotting results of OGN, ROR2, and HSPB1 confirmed the accuracy of the data. Bioinformatics analysis showed that 13 proteins may be linked to follicular development. Findings from this study will provide useful information for exploring follicular development and function.

Sections du résumé

BACKGROUND BACKGROUND
Characterization of molecular factors regulating ovarian follicular development is critical to understanding its functional mechanism of controlling the estrous cycle, determining oocyte competency, and regulating ovulation. In previous studies, we performed next-gene sequencing to investigate the differentially expressed transcripts of bovine follicular granulosa cells (GCs) at the dominant follicle (DF) and subordinate follicle (SF) stages during the first follicular wave. This study aims to investigate the proteomic characterization of GCs of DF and SF in the bovine estrous cycle.
RESULTS RESULTS
In total, 3409 proteins were identified from 30,321 peptides obtained from liquid chromatograph-mass spectrometer analysis. Two hundred fifty-nine of these proteins were found to be expressed differently in DF and SF. Out of 259, a total of 26 proteins were upregulated (fold change≥2) and 233 proteins were downregulated (fold change≤0.5) in DF. Gene Ontology (GO) analysis of proteome data revealed the biological process, cellular component and molecular function of expressed proteins in DF and SF, while the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed important signaling pathways associated with follicular development such as the PI3K-Akt, estrogen, and insulin signaling pathways. Immunoblotting results of OGN, ROR2, and HSPB1 confirmed the accuracy of the data. Bioinformatics analysis showed that 13 proteins may be linked to follicular development.
CONCLUSIONS CONCLUSIONS
Findings from this study will provide useful information for exploring follicular development and function.

Identifiants

pubmed: 31293364
doi: 10.1186/s41065-019-0097-5
pii: 97
pmc: PMC6593542
doi:

Substances chimiques

Proteome 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

21

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

Références

Mol Endocrinol. 1999 Jun;13(6):866-78
pubmed: 10379886
Biol Reprod. 2001 Aug;65(2):345-50
pubmed: 11466199
Anim Reprod Sci. 2001 Sep 15;67(3-4):189-203
pubmed: 11530265
Biol Reprod. 2002 Jan;66(1):70-6
pubmed: 11751266
Annu Rev Physiol. 2002;64:69-92
pubmed: 11826264
Endocrinology. 1955 Aug;57(2):193-9
pubmed: 13251223
Biol Reprod. 1992 Nov;47(5):871-83
pubmed: 1477213
J Endocrinol. 2006 Feb;188(2):215-25
pubmed: 16461548
Cell Signal. 2006 Sep;18(9):1351-9
pubmed: 16616457
Genes Dev. 2007 Apr 15;21(8):886-97
pubmed: 17437995
Biol Reprod. 2009 Sep;81(3):580-6
pubmed: 19439726
Reproduction. 2010 May;139(5):871-81
pubmed: 20197373
Development. 2011 Jan;138(1):9-22
pubmed: 21138973
J Reprod Fertil. 1990 Sep;90(1):267-77
pubmed: 2121972
Reprod Fertil Dev. 2011;23(1):32-9
pubmed: 21366978
Soc Reprod Fertil Suppl. 2010;67:105-17
pubmed: 21755666
Biochem Soc Trans. 2012 Feb;40(1):124-8
pubmed: 22260677
Res Vet Sci. 2013 Dec;95(3):1059-67
pubmed: 23937990
Proc Natl Acad Sci U S A. 2013 Oct 22;110(43):17474-9
pubmed: 24082083
Cell Commun Signal. 2015 Jan 29;13:6
pubmed: 25630770
Theriogenology. 2015 Apr 15;83(7):1179-87
pubmed: 25662108
J Neurooncol. 2016 Feb;126(3):405-13
pubmed: 26526033
Adv Exp Med Biol. 2017;1043:427-453
pubmed: 29224106
Endocrinol Metab Clin North Am. 1988 Dec;17(4):751-69
pubmed: 3143567
Biol Reprod. 1994 Feb;50(2):225-32
pubmed: 8142540
Biol Reprod. 1998 Feb;58(2):558-65
pubmed: 9475414
Biol Reprod. 1998 Sep;59(3):599-605
pubmed: 9716559

Auteurs

Qingling Hao (Q)

1College of Life Science, Shanxi Agricultural University, Taigu, 030801 Shanxi China.

Zhiwei Zhu (Z)

1College of Life Science, Shanxi Agricultural University, Taigu, 030801 Shanxi China.

Dongmei Xu (D)

1College of Life Science, Shanxi Agricultural University, Taigu, 030801 Shanxi China.

Wenzhong Liu (W)

2College of Animal Science and Technology, Shanxi Agricultural University, Taigu, 030801 Shanxi China.

Lihua Lyu (L)

2College of Animal Science and Technology, Shanxi Agricultural University, Taigu, 030801 Shanxi China.

Pengfei Li (P)

1College of Life Science, Shanxi Agricultural University, Taigu, 030801 Shanxi China.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH