Both N- and C-terminal domains of RelB are required for full transactivation: role of the N-terminal leucine zipper-like motif

Mol Cell Biol. 1993 Mar;13(3):1572-82. doi: 10.1128/mcb.13.3.1572-1582.1993.

Abstract

RelB, a member of the Rel family of transcription factors, can stimulate promoter activity in the presence of p50-NF-kappa B or p50B/p49-NF-kappa B in mammalian cells. Transcriptional activation analysis reveals that the N and C termini of RelB are required for full transactivation in the presence of p50-NF-kappa B. RelB/p50-NF-kappa B hybrid molecules containing the Rel homology domain of p50-NF-kappa B and the N and C termini of RelB have high transcriptional activity compared with wild-type p50-NF-kappa B. The N and C termini of RelB cooperate in transactivation in cis or trans configuration. Alterations in the structure of the leucine zipper-like motif present in the N terminus of RelB significantly decrease the transcriptional capacity of RelB and of different RelB/p50-NF-kappa B hybrid molecules.

Publication types

  • Comparative Study

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell-Free System
  • Cells, Cultured
  • DNA-Binding Proteins
  • Humans
  • Leucine Zippers*
  • Mice
  • Molecular Sequence Data
  • Oncogene Proteins v-rel
  • Retroviridae Proteins, Oncogenic / genetics*
  • Structure-Activity Relationship
  • Trans-Activators / genetics*
  • Transcription, Genetic*
  • Transcriptional Activation / genetics*
  • Transfection

Substances

  • DNA-Binding Proteins
  • Oncogene Proteins v-rel
  • Retroviridae Proteins, Oncogenic
  • Trans-Activators