Abstract

Despite the success of cloning technology in the production of offspring across several species, its application on a wide scale is severely limited by the very low offspring rate obtained with cloned embryos. The expression profile of microRNAs (miRNAs) in cloned embryos throughout embryonic development is reported to deviate from regular patterns. The present study is aimed at determining the dynamics of the global expression of miRNA profile in cloned and in-vitro fertilization (IVF) pre-implantation embryos at different developmental stages, i.e., the two-cell, eight-cell, and blastocyst stages, using next-generation sequencing. The results of this study suggest that there is a profound difference in global miRNA profile between cloned and IVF embryos. These differences are manifested throughout the course of embryonic development. The cloned embryos differ from their IVF counterparts in enriched Gene Ontology (GO) terms of biological process, molecular function, cellular component, and protein class categories in terms of the targets of differentially expressed miRNAs. The major pathways related to embryonic development, such as the Wnt signaling pathway, the apoptosis signaling pathway, the FGF signaling pathway, the p53 pathway, etc., were found to be affected in cloned relative to IVF embryos. Overall, these data reveal the distinct miRNA profile of cloned relative to IVF embryos, suggesting that the molecules or pathways affected may play an important role in cloned embryo development.

Highlights

  • Cloning by somatic cell nuclear transfer (SCNT) is one of the most important reproductive technologies

  • To date there is very little is known in regard to miRNAs and their potent role during embryonic development in mammalian species

  • Cuthbert and co-workers examined the dynamic shifts in the profile of small non-coding RNAs in terms of their relative abundance during the maternal-to-embryonic transition period in the different developmental stages of SCNT and in-vitro fertilization (IVF) embryos, i.e., two-cell, eight-cell, and morula, along with blastocyst-derived cells and donor cells used for cloning in cattle

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Summary

Introduction

Cloning by somatic cell nuclear transfer (SCNT) is one of the most important reproductive technologies. MiRNAs are involved in the regulation of many important events in reproduction, such as oocyte maturation and fertilization [27], embryo development [28–30], and maternal-to-embryonic transition [31]. Since their discovery, miRNAs have been among the most extensively studied molecules. There is no report on the global miRNA expression profile of cloned embryos and its comparison with that of their IVF counterparts at different developmental stages in any species. The present study was, carried out to study the dynamic of the global expression of miRNA profile in cloned and IVF pre-implantation embryos at different developmental stages using next-generation sequencing.

Materials and Methods
Production of Pre-Implantation Embryos by Hand-Made Cloning (HMC)
Production of Pre-Implantation Embryos by IVF
Extraction of Total RNA for Small-RNA Sequencing
Validation of RNA-seq Data by qPCR
Identification of Differentially Expressed miRNAs in Pre-Implantation Embryos
Identification of Commonly and Uniquely Expressed miRNAs
Pathway Identification and Network Analysis
Validation of RNA-seq Data
Discussion
Findings
Ethics Approval
Full Text
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