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Updated: Jun 11, 2026

Functional Cloning Using a Xenopus Oocyte Expression System
Published on: January 30, 2016
Identification of inappropriately reprogrammed genes by large-scale transcriptome analysis of individual cloned mouse
Atsushi Fukuda1, Feng Cao, Shinnosuke Morita
1Department of Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Abstract:
Although cloned embryos generated by somatic/embryonic stem cell nuclear transfer (SECNT) certainly give rise to viable individuals, they can often undergo embryonic arrest at any stage of embryogenesis, leading to diverse morphological abnormalities. In an effort to gain further insights into reprogramming and the properties of SECNT embryos, we performed a large-scale gene expression profiling of 87 single blastocysts using GeneChip microarrays. Sertoli cells, cumulus cells, and embryonic stem cells were used as donor cells. The gene expression profiles of 87 blastocysts were subjected to microarray analysis. Using principal component analysis and hierarchical clustering, the gene expression profiles were clearly classified into 3 clusters corresponding to the type of donor cell. The results revealed that each type of SECNT embryo had a unique gene expression profile that was strictly dependent upon the type of donor cells, although there was considerable variation among the individual profiles within each group. This suggests that the reprogramming process is distinct for embryos cloned from different types of donor cells. Furthermore, on the basis of the results of comparison analysis, we identified 35 genes that were inappropriately reprogrammed in most of the SECNT embryos; our findings demonstrated that some of these genes, such as Asz1, Xlr3a and App, were appropriately reprogrammed only in the embryos with a transcriptional profile that was the closest to that of the controls. Our findings provide a framework to further understand the reprogramming in SECNT embryos.
Insights
Somatic/embryonic stem cell nuclear transfer (SECNT) embryos show unique gene expression profiles based on donor cell type. Reprogramming differs between donor cells, impacting gene expression in cloned embryos.
Area of Science:
- Developmental Biology
- Genomics
- Reproductive Science
Background:
- Somatic/embryonic stem cell nuclear transfer (SECNT) cloning can result in embryonic arrest and abnormalities.
- Understanding the reprogramming process in SECNT embryos is crucial for improving cloning efficiency.
Purpose of the Study:
- To investigate the gene expression profiles of SECNT embryos using large-scale profiling.
- To determine if donor cell type influences the reprogramming process and gene expression in cloned embryos.
Main Methods:
- Gene expression profiling of 87 single blastocysts using GeneChip microarrays.
- Analysis of blastocysts derived from Sertoli cells, cumulus cells, and embryonic stem cells.
- Application of principal component analysis and hierarchical clustering for data classification.
Main Results:
- Gene expression profiles of SECNT embryos clustered distinctly based on donor cell type.
- Each donor cell type yielded unique gene expression profiles, indicating distinct reprogramming processes.
- Identified 35 genes with inappropriate reprogramming, with some corrected in embryos closest to control profiles.
Conclusions:
- Donor cell type significantly dictates the gene expression profile and reprogramming efficiency in SECNT embryos.
- This study provides a framework for understanding reprogramming variations in cloned embryos.
- Identified specific genes critical for successful reprogramming in cloned embryos.

