Structural basis of host protein hijacking in human T-cell leukemia virus integration

  • Veer Bhatt
  • , Ke Shi
  • , Daniel J. Salamango
  • , Nicholas H. Moeller
  • , Krishan K. Pandey
  • , Sibes Bera
  • , Thomas E. Bohl
  • , Fredy Kurniawan
  • , Kayo Orellana
  • , Wei Zhang
  • , Duane P. Grandgenett
  • , Reuben S. Harris
  • , Anna C. Sundborger-Lunna
  • , Hideki Aihara

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

Integration of the reverse-transcribed viral DNA into host chromosomes is a critical step in the life-cycle of retroviruses, including an oncogenic delta(δ)-retrovirus human T-cell leukemia virus type-1 (HTLV-1). Retroviral integrase forms a higher order nucleoprotein assembly (intasome) to catalyze the integration reaction, in which the roles of host factors remain poorly understood. Here, we use cryo-electron microscopy to visualize the HTLV-1 intasome at 3.7-Å resolution. The structure together with functional analyses reveal that the B56γ (B’γ) subunit of an essential host enzyme, protein phosphatase 2 A (PP2A), is repurposed as an integral component of the intasome to mediate HTLV-1 integration. Our studies reveal a key host-virus interaction underlying the replication of an important human pathogen and highlight divergent integration strategies of retroviruses.

Original languageEnglish (US)
Article number3121
JournalNature communications
Volume11
Issue number1
DOIs
StatePublished - Dec 1 2020
Externally publishedYes

ASJC Scopus subject areas

  • General Chemistry
  • General Biochemistry, Genetics and Molecular Biology
  • General Physics and Astronomy

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