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.

Plos One
|July 9, 2010
PubMed

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.