YY1 is involved in RANKL-induced transcription of the tartrate-resistant acid phosphatase gene in osteoclast differentiation

Gene. 2004 Dec 8;343(1):117-26. doi: 10.1016/j.gene.2004.08.009.

Abstract

Receptor activator of nuclear factor kappa B (NF-kappaB) ligand (RANKL), a critical activator of osteoclast differentiation, plays a pivotal role in tartrate-resistant acid phosphatase (TRAP) gene expression. Previously, we showed that upstream stimulatory factors (USF) 1 and 2 are implicated in the RANKL-induced TRAP transcriptional activation via a 12-bp USF binding site in the TRAP promoter. In that study, we also demonstrated that a RANKL-induced nuclear protein binds to a 50-bp oligonucleotide (Oligo IV) corresponding to a distinct TRAP promoter region. Here we report the identification and functional characterization of the nuclear protein binding to Oligo IV. We identified a 21-bp sequence CTGTTTATGATGGCGAGGGGG in Oligo IV that specifically binds the RANKL-induced nuclear protein from RAW264.7 cells by performing a series of competition assays. Computer analysis of the 21-bp sequence revealed that the sequence contains a putative Yin Yang 1 (YY1) binding site overlapped with a putative activator protein-2 (AP-2) binding site. Competition and supershift assays indicated that the nuclear protein binding to the 21-bp sequence is YY1, not AP-2. Functionally, mutation of the YY1-binding site resulted in a reduction in the RANKL-induced TRAP transcription in RAW264.7 cells, demonstrating that YY1 positively regulates RANKL-induced TRAP transcriptional activation. In conclusion, our data demonstrated that YY1 plays a functional role in RANKL-mediated TRAP gene expression during osteoclast differentiation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acid Phosphatase / genetics*
  • Animals
  • Base Sequence
  • Binding Sites
  • Carrier Proteins
  • Cell Differentiation / physiology*
  • Cell Line
  • Cell Nucleus / genetics
  • Cell Nucleus / physiology
  • Cell Nucleus / ultrastructure
  • DNA Primers
  • DNA-Binding Proteins / metabolism*
  • Erythroid-Specific DNA-Binding Factors
  • Isoenzymes / genetics*
  • Membrane Glycoproteins
  • Mice
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • NF-kappa B / metabolism
  • Osteoclasts / cytology*
  • Osteoclasts / physiology
  • Promoter Regions, Genetic
  • RANK Ligand
  • Receptor Activator of Nuclear Factor-kappa B
  • Repressor Proteins / metabolism
  • Tartrate-Resistant Acid Phosphatase
  • Transcription Factor AP-1 / metabolism
  • Transcription Factors / metabolism*
  • Transcription, Genetic*
  • Transfection
  • YY1 Transcription Factor

Substances

  • Carrier Proteins
  • DNA Primers
  • DNA-Binding Proteins
  • Erythroid-Specific DNA-Binding Factors
  • Isoenzymes
  • Membrane Glycoproteins
  • NF-kappa B
  • RANK Ligand
  • Receptor Activator of Nuclear Factor-kappa B
  • Repressor Proteins
  • Tnfrsf11a protein, mouse
  • Tnfsf11 protein, mouse
  • Transcription Factor AP-1
  • Transcription Factors
  • YY1 Transcription Factor
  • Yy1 protein, mouse
  • Acid Phosphatase
  • Acp5 protein, mouse
  • Tartrate-Resistant Acid Phosphatase