Transcriptional repression by XPc1, a new Polycomb homolog in Xenopus laevis embryos, is independent of histone deacetylase

J Strouboulis, S Damjanovski, D Vermaak, F Meric, A P Wolffe

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

The Polycomb group (Pc-G) genes encode proteins that assemble into complexes implicated in the epigenetic maintenance of heritable patterns of expression of developmental genes, a function largely conserved from Drosophila to mammals and plants. The Pc-G is thought to act at the chromatin level to silence expression of target genes; however, little is known about the molecular basis of this repression. In keeping with the evidence that Pc-G homologs in higher vertebrates exist in related pairs, we report here the isolation of XPc1, a second Polycomb homolog in Xenopus laevis. We show that XPc1 message is maternally deposited in a translationally masked form in Xenopus oocytes, with XPc1 protein first appearing in embryonic nuclei shortly after the blastula stage. XPc1 acts as a transcriptional repressor in vivo when tethered to a promoter in Xenopus embryos. We find that XPc1-mediated repression can be only partially alleviated by an increase in transcription factor dosage and that inhibition of deacetylase activity by trichostatin A treatment has no effect on XPc1 repression, suggesting that histone deacetylation does not form the basis for Pc-G-mediated repression in our assay.

Original languageEnglish
Pages (from-to)3958-68
Number of pages11
JournalMolecular and Cellular Biology
Volume19
Issue number6
DOIs
Publication statusPublished - Jun 1999

Keywords

  • Amino Acid Sequence
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Cell Nucleus/metabolism
  • Centrifugation, Density Gradient
  • Enzyme Inhibitors/pharmacology
  • Gene Expression Regulation, Developmental
  • Genes, Reporter
  • Histone Deacetylases/physiology
  • Hydroxamic Acids/pharmacology
  • Molecular Sequence Data
  • Phosphorylation
  • Repressor Proteins/genetics
  • Sequence Homology, Amino Acid
  • Time Factors
  • Tissue Distribution
  • Transcription Factors
  • Transcription, Genetic
  • Xenopus Proteins
  • Xenopus laevis/embryology

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