Cited by 516T-cell and Retrovirus StudiesHIV Research and TreatmentViral-associated cancers and disorders

The pX protein of HTLV-I is a transcriptional activator of its long terminal repeats

Felber, Barbara K., Paskalis, Harry, Kleinman-Ewing, Carol, Wong-Staal, Flossie, Pavlakis, George N.·1985·Science

Abstract

Expression of the pX protein of human T-cell leukemia virus type I (HTLV-I) in animal cells demonstrates that this protein is a specific transcriptional activator of the long terminal repeats (LTR) of HTLV-I. Several other promoters are not affected by pX. No lymphocyte-specific factors are required for this activation. pX can be detected in the nucleus of transfected monkey kidney cells (line CV1) by indirect immunofluorescence. These results indicate that the pX protein is essential for the replication cycle of the virus and that it may be directly involved in the immortalization of human lymphocytes by HTLV-I.

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Crossref · 10.1126/science.2992082

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  • Following infection, HTLV-1 is integrated into host cell chromatin, and the LTRs act as promoters for both the sense and anti-sense strand directions.

    “Following infection, HTLV-1 is integrated into the host cell chromatin, and the LTRs act as promoters for both the sense and anti-sense strand directions [29], expressing multiple gene products detailed in Table 1.”

    From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [29]

  • Like HIV-1, HTLV-1 contains trans-acting regulators of transcription in the form of Tax protein and a Tax responsive element (TRE) in the LTR.

    “Like HIV-1, HTLV-1 also contains trans-acting regulators of transcription in the form of Tax (protein) and Tax responsive element (TRE) in the LTR (Sodroski et al. 1984, Cann et al. 1985, Felber et al. 1985, Fujisawa et al. 1985).”

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Authors
Felber, B. K., Paskalis, H., Kleinman-Ewing, C., Wong-Staal, F., & Pavlakis, G. N.
Affiliations
  • Frederick National Laboratory for Cancer Research (US)
  • Laboratory of Tumor Cell Biology, National Cancer Institute, Bethesda, Maryland 20205
Venue
Science
Published
1985-08-16
Volume
229
Issue
4714
Pages
675-679
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1998461588
Cited by
516
References
1
Citations by year
2026: 3 · 2025: 3 · 2024: 3 · 2023: 5 · 2022: 7 · 2021: 2 · 2020: 3 · 2019: 5 · 2018: 3 · 2017: 4 · 2016: 2 · 2015: 4 · 2014: 8 · 2013: 6 · 2012: 6
FWCI
15.04
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
Funders
U.S. Public Health Service (N01-C0-23909)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Health Sciences › Medicine › Oncology › Viral-associated cancers and disorders
Keywords
HTLV-1, long terminal repeat, transcriptional activation, viral replication, lymphocyte immortalization, T-cell leukemia virus, nuclear localization, transcriptional activator
MeSH terms
DNA, Recombinant, Gene Expression Regulation, Peptides, Plasmids, Promoter Regions, Genetic, Repetitive Sequences, Nucleic Acid, DNA-Directed RNA Polymerases, Transcription Factors, Transcription, Genetic, Viral Proteins, Transforming Growth Factors, Deltaretrovirus

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