Human gamma-satellite DNA maintains open chromatin structure and protects a transgene from epigenetic silencing

  • Jung Hyun Kim
  • , Thomas Ebersole
  • , Natalay Kouprina
  • , Vladimir N. Noskov
  • , Jun Ichirou Ohzeki
  • , Hiroshi Masumoto
  • , Brankica Mravinac
  • , Beth A. Sullivan
  • , Adam Pavlicek
  • , Sinisa Dovat
  • , Svetlana D. Pack
  • , Yoo Wook Kwon
  • , Patrick T. Flanagan
  • , Dmitri Loukinov
  • , Victor Lobanenkov
  • , Vladimir Larionov

Research output: Contribution to journalArticlepeer-review

57 Scopus citations

Abstract

The role of repetitive DNA sequences in pericentromeric regions with respect to kinetochore/heterochromatin structure and function is poorly understood. Here, we use a mouse erythroleukemia cell (MEL) system for studying how repetitive DNA assumes or is assembled into different chromatin structures. We show that human gamma-satellite DNA arrays allow a transcriptionally permissive chromatin conformation in an adjacent transgene and efficiently protect it from epigenetic silencing. These arrays contain CTCF and Ikaros binding sites. In MEL cells, this gamma-satellite DNA activity depends on binding of Ikaros proteins involved in differentiation along the hematopoietic pathway. Given our discovery of gamma-satellite DNA in pericentromeric regions of most human chromosomes and a dynamic chromatin state of gamma-satellite arrays in their natural location, we suggest that gamma-satellite DNA represents a unique region of the functional centromere with a possible role in preventing heterochromatin spreading beyond the pericentromeric region.

Original languageEnglish (US)
Pages (from-to)533-544
Number of pages12
JournalGenome research
Volume19
Issue number4
DOIs
StatePublished - Apr 2009

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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