Gene expression profiling of embryo-derived stem cells reveals candidate genes associated with pluripotency and lineage specificity

Genome Res. 2002 Dec;12(12):1921-8. doi: 10.1101/gr.670002.

Abstract

Large-scale gene expression profiling was performed on embryo-derived stem cell lines to identify molecular signatures of pluripotency and lineage specificity. Analysis of pluripotent embryonic stem (ES) cells, extraembryonic-restricted trophoblast stem (TS) cells, and terminally-differentiated mouse embryo fibroblast (MEF) cells identified expression profiles unique to each cell type, as well as genes common only to ES and TS cells. Whereas most of the MEF-specific genes had been characterized previously, the majority (67%) of the ES-specific genes were novel and did not include known differentiated cell markers. Comparison with microarray data from embryonic material demonstrated that ES-specific genes were underrepresented in all stages sampled, whereas TS-specific genes included known placental markers. Investigation of four novel TS-specific genes showed trophoblast-restricted expression in cell lines and in vivo, whereas one uncharacterized ES-specific gene, Esg-1, was found to be exclusively associated with pluripotency. We suggest that pluripotency requires a set of genes not expressed in other cell types, whereas lineage-restricted stem cells, like TS cells, express genes predictive of their differentiated lineage.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Cell Line
  • Cell Lineage / genetics
  • DNA, Complementary / genetics
  • DNA-Binding Proteins / genetics
  • Embryo, Mammalian / cytology*
  • Embryo, Mammalian / physiology*
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation, Developmental / genetics*
  • Genes, Essential / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Multigene Family / genetics
  • Octamer Transcription Factor-3
  • Oligonucleotide Array Sequence Analysis / methods*
  • Organ Specificity / genetics
  • Pluripotent Stem Cells / chemistry
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / physiology*
  • Proteins / genetics
  • Totipotent Stem Cells / chemistry
  • Totipotent Stem Cells / physiology
  • Transcription Factors / genetics
  • Trophoblasts / chemistry
  • Trophoblasts / cytology
  • Trophoblasts / physiology
  • Xenopus Proteins*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • DNA, Complementary
  • DNA-Binding Proteins
  • Octamer Transcription Factor-3
  • Pou5f1 protein, mouse
  • Proteins
  • TLE1 protein, Xenopus
  • Transcription Factors
  • Xenopus Proteins