Human immunodeficiency virus type 1 Vpu and cellular TASK proteins suppress transcription of unintegrated HIV-1 DNA

Virol J. 2012 Nov 19:9:277. doi: 10.1186/1743-422X-9-277.

Abstract

Background: Unintegrated HIV-1 DNA serves as transcriptionally active templates in HIV-infected cells. Several host factors including NF-κβ enhance HIV-1 transcription. HIV-1 induced NF-κβ activation can be suppressed by viral protein U (Vpu). Interestingly HIV-1 Vpu shares amino acid homology with cellular Twik-related Acid Sensitive K+ (TASK) channel 1 and the proteins physically interact in cultured cells and AIDS lymphoid tissue. Furthermore, the first transmembrane domain of TASK-1 is functionally interchangeable with Vpu and like Vpu enhances HIV-1 release.

Results: Here we further characterize the role of TASK channels and Vpu in HIV-1 replication. We demonstrate that both TASK channels and Vpu can preferentially inhibit transcription of unintegrated HIV-1 DNA. Interestingly, TASK-1 ion channel function is not required and suppression of HIV-1 transcription by TASK-1 and Vpu was reversed by overexpression of RelA (NF-κβ p65).

Conclusion: TASK proteins and Vpu suppress transcription of unintegrated HIV-1 DNA through an NF-κβ-dependent mechanism. Taken together these findings support a possible physiological role for HIV-1 Vpu and TASK proteins as modulators of transcription of unintegrated HIV-1 DNA genomes.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • DNA, Viral / genetics
  • DNA, Viral / metabolism*
  • Gene Expression Regulation, Viral
  • HEK293 Cells
  • HIV Infections / virology
  • HIV Integrase / genetics
  • HIV Integrase / metabolism
  • HIV-1 / genetics*
  • HIV-1 / metabolism
  • HIV-1 / physiology
  • Human Immunodeficiency Virus Proteins / genetics
  • Human Immunodeficiency Virus Proteins / metabolism*
  • Humans
  • Ion Channels / metabolism
  • Jurkat Cells
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Potassium Channels, Tandem Pore Domain / genetics
  • Potassium Channels, Tandem Pore Domain / metabolism*
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / metabolism
  • Transcription, Genetic*
  • Transfection
  • Viral Regulatory and Accessory Proteins / genetics
  • Viral Regulatory and Accessory Proteins / metabolism*
  • Virus Integration*
  • Virus Replication

Substances

  • DNA, Viral
  • Human Immunodeficiency Virus Proteins
  • Ion Channels
  • Nerve Tissue Proteins
  • Potassium Channels, Tandem Pore Domain
  • RELA protein, human
  • Transcription Factor RelA
  • Viral Regulatory and Accessory Proteins
  • vpu protein, Human immunodeficiency virus 1
  • potassium channel subfamily K member 3
  • HIV Integrase