Home LiteratureArticle Details
PMID: 34623529 Published · epublish English Journal Article

Transcriptome comparisons detect new genes associated with apoptosis of cattle and buffaloes preantral follicles.

Journal, genetic engineering & biotechnology ·Vol. 19 ·No. 1 ·2021-10-08 ·Pages 151

Zoheir KM, Darwish AM, Liguo Y, Ashour AE

Abstract

To develop new breeding technology to improve the breeding ability of bovine, it is the development trend to find the main reason for the occurrence of atresia in these organisms. Transcriptomes of small (100-120 μm) and large (200-220 μm) preantral follicles from cattle and buffalo ovaries were evaluated in vivo and in vitro to understand the transcriptional modulation in preantral follicles that leads to the phenomenon of atresia. The preantral follicles were checked as dead, damage, or live follicles in vivo and in vitro by using trypan blue then bisbenzimide and propidium iodine. Transcriptomes of small (100-120 μm) and large (200-220 μm) preantral follicles of cattle and buffalo were evaluated in vivo and in vitro by microarray and RT-PCR. Healthy preantral follicles were selected based on staining results, and then RNA was extracted from them. The viability percentage of preantral follicles in cattle was higher (26.7% and 20%) than buffalo (10%) in vivo and in vitro, respectively. According to the microarray data analysis for cattle preantral follicles, only eleven genes were detected corresponding to five upregulated and six downregulated in large size (200-220 μm) compared to small (100-120 μm) size preantral follicles, while in buffalo, 171 genes were detected (92 upregulated and 79 downregulated) in large size compared to small preantral follicle size. The results of RT-PCR of the selected genes (FASTKD1, BAG2, RHOB, AGTR2, MEF2C, BCL10, G2E3, TM2D1, IGF-I, IGFBP3, PRDX3, and TRIAP1) validated the microarray results. In conclusion, the data of gene expression showed significant differences between small and large sizes in both buffalo and cattle preantral follicles. Apoptotic genes were upregulated in the large preantral follicle compared with the small preantral follicles. Moreover, the expression level of these apoptotic genes was significantly upregulated in buffalo than in the cattle. Most of these genes were significantly upregulated in the large buffalo preantral follicle compared with the small size. However, anti-apoptotic genes were upregulated in large cattle preantral follicle and downregulated in large buffalo preantral follicle.

Keywords
Apoptosis Atresia Buffalo Cattle Gene expression Preantral follicles
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zoheir Khairy Mohamed ORCID
Cell Biology Department, National Research Centre, Dokki, 12622, Egypt. khma25@gmail.com.
Darwish Ahmed Mohamed
Cell Biology Department, National Research Centre, Dokki, 12622, Egypt.
Liguo Yang
Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, People's Republic of China.
Ashour Abdelkader E
Department of Basic Medical Sciences, Kulliyyah of Medicine, International Islamic University Malaysia, 25200, Kuantan, Pahang Darul Makmur, Malaysia.
References (26)
26 references, click to expand
  1. Induction of BAG2 protein during proteasome inhibitor-induced apoptosis in thyroid carcinoma cells.
    Br J Pharmacol. 2008 Nov;155(5):655-60 PMID: 18660828
  2. Laboratory production of buffalo (Bubalus bubalis) embryos.
    Reprod Fertil Dev. 1998;10(5):379-91 PMID: 10461670
  3. The FASTK family of proteins: emerging regulators of mitochondrial RNA biology.
    Nucleic Acids Res. 2017 Nov 2;45(19):10941-10947 PMID: 29036396
  4. The novel cyclophilin-D-interacting protein FASTKD1 protects cells against oxidative stress-induced cell death.
    Am J Physiol Cell Physiol. 2019 Sep 1;317(3):C584-C599 PMID: 31268778
  5. Apoptosis: a review of programmed cell death.
    Toxicol Pathol. 2007 Jun;35(4):495-516 PMID: 17562483
  6. siRNA targeting of PRDX3 enhances cisplatin‑induced apoptosis in ovarian cancer cells through the suppression of the NF‑κB signaling pathway.
    Mol Med Rep. 2013 May;7(5):1688-94 PMID: 23503975
  7. Autophagy in Ovarian Follicular Development and Atresia.
    Int J Biol Sci. 2019 Jan 29;15(4):726-737 PMID: 30906205
  8. The role of p53 in apoptosis.
    Discov Med. 2010 Feb;9(45):145-52 PMID: 20193641
  9. Effect of LH on circulating oestradiol and follicular fluid factor concentrations during follicle deviation in cattle.
    Reproduction. 2001 Jul;122(1):103-10 PMID: 11425334
  10. Release of Cytochrome C from Bax Pores at the Mitochondrial Membrane.
    Sci Rep. 2017 Jun 1;7(1):2635 PMID: 28572603
  11. The angiotensin type 2 receptor of angiotensin II and neuronal differentiation: from observations to mechanisms.
    J Mol Endocrinol. 2003 Dec;31(3):359-72 PMID: 14664700
  12. Multiple functions of peroxiredoxins: peroxidases, sensors and regulators of the intracellular messenger H₂O₂, and protein chaperones.
    Antioxid Redox Signal. 2011 Aug 1;15(3):781-94 PMID: 20919930
  13. Effects of pregnant mare serum gonadotropin (eCG) on follicle development and granulosa-cell apoptosis in the pig.
    Theriogenology. 2003 Feb;59(3-4):775-85 PMID: 12517381
  14. Quantification, morphology and ultrastructure of preantral follicles of buffalo (Bubalus bubalis) foetuses.
    Reprod Domest Anim. 2011 Feb;46(1):e17-22 PMID: 20403125
  15. Apoptosis in granulosa cells during follicular atresia: relationship with steroids and insulin-like growth factors.
    Cell Res. 2004 Aug;14(4):341-6 PMID: 15353131
  16. Caspase functions in cell death and disease.
    Cold Spring Harb Perspect Biol. 2013 Apr 01;5(4):a008656 PMID: 23545416
  17. Antral follicle count reliably predicts number of morphologically healthy oocytes and follicles in ovaries of young adult cattle.
    Biol Reprod. 2008 Dec;79(6):1219-25 PMID: 18768912
  18. RhoB upregulation leads to either apoptosis or cytostasis through differential target selection.
    Endocr Relat Cancer. 2015 Oct;22(5):777-92 PMID: 26206775
  19. Mitochondria in apoptosis: Bcl-2 family members and mitochondrial dynamics.
    Dev Cell. 2011 Jul 19;21(1):92-101 PMID: 21763611
  20. Co-chaperone BAG2 Determines the Pro-oncogenic Role of Cathepsin B in Triple-Negative Breast Cancer Cells.
    Cell Rep. 2017 Dec 5;21(10):2952-2964 PMID: 29212038
  21. Myocyte enhancer factor 2C as a neurogenic and antiapoptotic transcription factor in murine embryonic stem cells.
    J Neurosci. 2008 Jun 25;28(26):6557-68 PMID: 18579729
  22. Antisense oligonucleotide to insulin-like growth factor II induces apoptosis in human ovarian cancer AO cell line.
    Cell Res. 1998 Jun;8(2):159-65 PMID: 9669031
  23. Oocyte retrieval and histological studies of follicular population in buffalo ovaries.
    Anim Reprod Sci. 1997 Jun;47(3):189-95 PMID: 9329860
  24. Insulin-like growth factor I modulates induction of apoptotic signaling in H9C2 cardiac muscle cells.
    Endocrinology. 1998 Mar;139(3):1354-60 PMID: 9492072
  25. Development and senescence of the postnatal bovine ovary.
    J Anim Sci. 1966 Aug;25(3):800-5 PMID: 6007918
  26. TP53 Regulated Inhibitor of Apoptosis 1 (TRIAP1) stable silencing increases late apoptosis by upregulation of caspase 9 and APAF1 in RPMI8226 multiple myeloma cell line.
    Biochim Biophys Acta. 2016 Jun;1862(6):1105-10 PMID: 27032384
Article Info
Journal
Journal, genetic engineering & biotechnology
Abbr.
J Genet Eng Biotechnol
ISSN
2090-5920
Published
2021-10-08
Epub
2021-00-08
Pages
151
Language
English
Region
Netherlands
NLM ID
101317150
PMCID
PMC8501173
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com