Evidence map›Paper›PMID 25673710›Full record

ArticleJournal of virology2015

A mutant tat protein inhibits HIV-1 reverse transcription by targeting the reverse transcription complex.

Min-Hsuan Lin, Ann Apolloni, Vincent Cutillas, Haran Sivakumaran, Sally Martin, Dongsheng Li, Ting Wei, Rui Wang, Hongping Jin, Kirsten Spann and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. HIV Genome-Wide Protein Associations: a Review of 30 Years of Research.Microbiology and molecular biology reviews : MMBR · 2016
    Pooled it
  2. Review
  3. Review
  4. Cure and Long-Term Remission Strategies.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  5. Review
  6. Article
  7. Review
  8. Block and Lock HIV Cure Strategies to Control the Latent Reservoir.Frontiers in cellular and infection microbiology · 2020
    Review
  9. StrongmBio · 2019
    Article
  10. Article
  11. Dopaminergic Regulation of Innate Immunity: a Review.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2017
    Review
  12. Article
  13. Review
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Min-Hsuan LinQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Ann ApolloniQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Vincent CutillasQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Haran SivakumaranQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Sally MartinClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St. Lucia, Queensland, Australia.
Dongsheng LiQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Ting WeiQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Rui WangQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Hongping JinQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Kirsten SpannSchool of Biomedical Science, Queensland University of Technology, Brisbane, Queensland, Australia.
David HarrichQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia Australian Infectious Disease Research Centre at the University of Queensland, St. Lucia, Queensland, Queensland, Australia david.harrich@qimrberghofer.edu.au.
QIMR Berghofer Medical Research Institute · AUPark Centre for Mental Health · AUQueensland University of Technology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledPreviously, we reported that a mutant of Tat referred to as Nullbasic inhibits HIV-1 reverse transcription although the mechanism of action is unknown. Here we show that Nullbasic is a reverse transcriptase (RT) binding protein that targets the reverse transcription complex rather than directly inhibiting RT activity. An interaction between Nullbasic and RT was observed by using coimmunoprecipitation and pulldown assays, and a direct interaction was measured by using a biolayer interferometry assay. Mixtures of recombinant 6×His-RT and Nullbasic-FLAG-V5-6×His at molar ratios of up to 1:20,000 did not inhibit RT activity in standard homopolymer primer template assays. An analysis of virus made by cells that coexpressed Nullbasic showed that Nullbasic copurified with virus particles, indicating that it was a virion protein. In addition, analysis of reverse transcription complexes (RTCs) isolated from cells infected with wild type or Nullbasic-treated HIV-1 showed that Nullbasic reduced the levels of viral DNA in RTC fractions. In addition, a shift in the distribution of viral DNA and CAp24 to less-dense non-RTC fractions was observed, indicating that RTC activity from Nullbasic-treated virus was impaired. Further analysis showed that viral cores isolated from Nullbasic-treated HIV undergo increased disassembly in vitro compared to untreated HIV-1. To our knowledge, this is the first description of an antiviral protein that inhibits reverse transcription by targeting the RTC and affecting core stability. IMPORTANCE: HIV-1 infection is treated by using combinations of antiretroviral drugs that target independent steps of virus replication. A newly described antiviral protein called Nullbasic can also inhibit a combination of different steps in virus replication (transcription, reverse transcription, and Rev-mediated viral mRNA transport), although the precise mechanism of action is unknown. This study shows that Nullbasic can inhibit reverse transcription by binding to the viral enzyme called reverse transcriptase, which results in accelerated uncoating of the viral core and instability of the viral apparatus called the reverse transcription complex (RTC). This unique antiviral activity may inform development of other RTC inhibitors, as well as providing a unique investigative tool for dissecting the RTC cellular composition.

Indexed as

Reverse TranscriptionCentrifugationHIV-1HIV Reverse TranscriptaseImmunoprecipitationMutant ProteinsProtein Bindingtat Gene Products, Human Immunodeficiency VirusHIV Reverse TranscriptaseMutant Proteinsreverse transcriptase, Human immunodeficiency virus 1tat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID25673710
PMCPMC4403448
OpenAlexW2171009653

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.