[Effect of RelB on HIV-1 Vpr-mediated transcription activation and cell G2/M arrest]

Bing Du Xue Bao. 2013 Jan;29(1):44-50.
[Article in Chinese]

Abstract

Vpr, an auxiliary protein of HIV-1(Human immunodeficiency virus type 1), exerts important functions to promote viral replication and AIDS progression. In this study, we performed a yeast two-hybrid screening assay using human cDNA library to further investigate the molecular mechanism of various functions of Vpr RelB, a key protein in NF-kappaB signaling pathway, was identified as a Vpr interaction protein by co-immunoprecipitation. Further investigations indicated that RelB not only promoted the Vpr-mediated activation of NF-kappaB reporter gene, but also enhanced the transactivation of HIV LTR. Moreover, the results showed that RelB promoted Vpr-induced cell cycle G2/M arrest. Collectively, these results indicated that RelB might interact with Vpr and regulate its transcriptional activation and cell cycle arrest.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Checkpoints*
  • Cell Division*
  • G2 Phase*
  • HIV Long Terminal Repeat
  • HeLa Cells
  • Humans
  • NF-kappa B / genetics
  • Transcription Factor RelB / physiology*
  • Transcriptional Activation*
  • vpr Gene Products, Human Immunodeficiency Virus / physiology*

Substances

  • NF-kappa B
  • RELB protein, human
  • vpr Gene Products, Human Immunodeficiency Virus
  • vpr protein, Human immunodeficiency virus 1
  • Transcription Factor RelB