Orf-I and orf-II-encoded proteins in HTLV-1 infection and persistence

Viruses. 2011 Jun;3(6):861-85. doi: 10.3390/v3060861. Epub 2011 Jun 17.


The 3' end of the human T-cell leukemia/lymphoma virus type-1 (HTLV-1) genome contains four overlapping open reading frames (ORF) that encode regulatory proteins. Here, we review current knowledge of HTLV-1 orf-I and orf-II protein products. Singly spliced mRNA from orf-I encodes p12, which can be proteolytically cleaved to generate p8, while differential splicing of mRNA from orf-II results in production of p13 and p30. These proteins have been demonstrated to modulate transcription, apoptosis, host cell activation and proliferation, virus infectivity and transmission, and host immune responses. Though these proteins are not essential for virus replication in vitro, p8, p12, p13, and p30 have an important role in the establishment and maintenance of HTLV-1 infection in vivo.

Keywords: HTLV-1; ORF-I; ORF-II; human T-cell leukemia/lymphoma virus type-1; p12; p13; p30; p8.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • HTLV-I Infections / virology*
  • Human T-lymphotropic virus 1 / genetics
  • Human T-lymphotropic virus 1 / metabolism*
  • Humans
  • Open Reading Frames*
  • RNA Splicing
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*


  • Viral Proteins