Expression of miR-302 in human embryo derived from in-vitro matured oocyte

Abstract Background The expression of miR-302 over the period of early embryogenesis could possibly regulate the maternal transcript clearance. Zygotic transcription activation is mostly related to maternal messages degradation. Objective In this study, the effects of in-vitro maturation technique (...

Full description

Saved in:
Bibliographic Details
Main Authors: Parvin Dorfeshan (Author), Marefat Ghaffari Novin (Author), Mohammad Salehi (Author), Fatane Farifteh (Author)
Format: Book
Published: Shahid Sadoughi University of Medical Sciences, 2019-06-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_e1286f15e6904ddc84ec3790ee660033
042 |a dc 
100 1 0 |a Parvin Dorfeshan  |e author 
700 1 0 |a Marefat Ghaffari Novin  |e author 
700 1 0 |a Mohammad Salehi  |e author 
700 1 0 |a Fatane Farifteh  |e author 
245 0 0 |a Expression of miR-302 in human embryo derived from in-vitro matured oocyte 
260 |b Shahid Sadoughi University of Medical Sciences,   |c 2019-06-01T00:00:00Z. 
500 |a 2476-3772 
500 |a 10.18502/ijrm.v17i6.4812 
520 |a Abstract Background The expression of miR-302 over the period of early embryogenesis could possibly regulate the maternal transcript clearance. Zygotic transcription activation is mostly related to maternal messages degradation. Objective In this study, the effects of in-vitro maturation technique (IVM) on the expression of miR-302 in human embryo produced from immature and mature human oocytes (matured in vitro and in vivo, before sperm exposure) obtained from females under gonadotrophin therapy were evaluated for assisted reproduction. Materials and Methods Immature oocytes were cultured in vitro. The injection of oocytes-producing polar bodies was given using fresh sperm. Then, the embryo quality score was assessed in the IVM group compared with the control group. In both the groups, embryos with normal morphology were included in the molecular study. Only one blastomere was removed from three-day embryos and then the embryos were frozen. The expression of miR-302 in embryos was measured through quantitative real-time polymerase chain reaction. Results Our data showed a significant reduction of miR-302 expression in the IVM group vs. the control group (p = 0.02). The embryo quality score showed a significant difference between the two groups (p = 0.01). Conclusion The present study demonstrated that the IVM process had a negative effect on the expression level of miR-302 in human pre-implantation embryos. Considering the major role of expression miR-302, a reduced potential in miR-302 expression could be related to a decrease in the early embryonic development. 
546 |a EN 
690 |a mir-302 
690 |a embryonic development 
690 |a ovarian stimulation 
690 |a in-vitro maturation 
690 |a intracytoplasmic sperm injection. 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
690 |a Reproduction 
690 |a QH471-489 
655 7 |a article  |2 local 
786 0 |n International Journal of Reproductive BioMedicine, Vol 17, Pp 405-412 (2019) 
787 0 |n https://doi.org/10.18502/ijrm.v17i6.4812 
787 0 |n https://doaj.org/toc/2476-3772 
856 4 1 |u https://doaj.org/article/e1286f15e6904ddc84ec3790ee660033  |z Connect to this object online.