Regulation of upstream binding factor 1 activity by insulin-like growth factor I receptor signaling

J Biol Chem. 2005 Jan 28;280(4):2863-72. doi: 10.1074/jbc.M406138200. Epub 2004 Nov 8.

Abstract

The upstream binding factor 1 (UBF1) is one of the proteins in a complex that regulates the activity of RNA polymerase I, which controls the rate of ribosomal RNA (rRNA) synthesis. We have shown previously that insulin receptor substrate-1 (IRS-1) can translocate to the nuclei and nucleoli of cells and bind UBF1. We report here that activation of the type I insulin-like growth factor receptor (IGF-IR) by IGF-I increases transcription from the ribosomal DNA (rDNA) promoter in both myeloid cells and mouse fibroblasts. The increased activity of the rDNA promoter is accompanied by increased phosphorylation of UBF1, a requirement for UBF1 activation. Phosphorylation occurs on a number of UBF1 peptides, most prominently on the highly acidic, serine-rich C terminus. In myeloid cells (but not in mouse embryo fibroblasts) IRS-1 signaling stabilizes the levels of UBF1 protein. These findings demonstrate that IGF-IR signaling can increase the activity of UBF1 and transcription from the rDNA promoter, providing one explanation for the reported effects of the IGF/IRS-1 axis on cell and body size in animals and cells in culture.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Cell Differentiation
  • Cell Nucleolus / metabolism
  • Cell Nucleus / metabolism
  • DNA, Ribosomal / chemistry
  • DNA, Ribosomal / metabolism
  • Exons
  • Fibroblasts / metabolism
  • Gene Expression Regulation*
  • Gene Expression Regulation, Developmental
  • Mice
  • Mutation
  • Peptides / chemistry
  • Phosphorylation
  • Phosphotyrosine / chemistry
  • Pol1 Transcription Initiation Complex Proteins / biosynthesis*
  • Pol1 Transcription Initiation Complex Proteins / genetics
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Structure, Tertiary
  • RNA, Messenger / metabolism
  • RNA, Ribosomal / metabolism
  • Receptor, IGF Type 1 / metabolism*
  • Ribosomes / chemistry
  • Ribosomes / metabolism
  • Time Factors
  • Transcription, Genetic
  • Trypsin / pharmacology

Substances

  • DNA, Ribosomal
  • Peptides
  • Pol1 Transcription Initiation Complex Proteins
  • RNA, Messenger
  • RNA, Ribosomal
  • transcription factor UBF
  • Phosphotyrosine
  • Receptor, IGF Type 1
  • Trypsin