Transcriptional regulation of mouse l-selectin

Xitong Dang, Nikolai A. Raffler, Klaus Ley

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

l-selectin mediates the initial tethering and rolling of lymphocytes in high endothelial venules. To study the transcriptional regulation of mouse l-selectin, we cloned 4.5 kb 5′-flanking sequences of the mouse sell. Luciferase analysis of serial 5′-deletion mutants showed that the first 285 bp was sufficient to drive high promoter activity in EL4 cells, but not in Sell-negative HeLa cells, suggesting that this fragment harbors the minimal mouse sell promoter and contains cis-elements for lymphocyte-specific expression. Site-directed mutagenesis and chromatin immunoprecipitation showed that Mzf1, Klf2, Sp1, Ets1, and Irf1 bind to and activate the mouse sell promoter. Over expression of these transcription factors in EL4 cells increased expression of sell mRNA. Silencing the expression of Sp1 by siRNA significantly decreased sell promoter activity in EL4 cells. We conclude that sell transcription is regulated by Mzf1, Klf2, Sp1, Ets1, and Irf1.

Original languageEnglish (US)
Pages (from-to)146-152
Number of pages7
JournalBiochimica et Biophysica Acta - Gene Regulatory Mechanisms
Volume1789
Issue number2
DOIs
StatePublished - Feb 2009
Externally publishedYes

Keywords

  • Ets-1
  • Gene regulation
  • Irf1
  • Klf2
  • Mzf-1
  • Promoter
  • Sp1
  • l-selectin

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics

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