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  4. Human immunodeficiency viruses regulated by alternative trans-activators: Genetic evidence for a novel non-transcriptional function of Tat in virion infectivity
 
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Human immunodeficiency viruses regulated by alternative trans-activators: Genetic evidence for a novel non-transcriptional function of Tat in virion infectivity

Journal
EMBO Journal
Journal Volume
13
Journal Issue
12
Pages
2886-2896
Date Issued
1994
Author(s)
LI-MIN HUANG  
Joshi A.
Willey R.
Orenstein J.
Jeang K.-T.
DOI
10.1002/j.1460-2075.1994.tb06583.x
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028318363&doi=10.1002%2fj.1460-2075.1994.tb06583.x&partnerID=40&md5=065f0c04147517e7916b084a84bf6e31
https://scholars.lib.ntu.edu.tw/handle/123456789/566723
Abstract
Thirteen genetically altered HIV-1 proviruses were created. These various genomes can be segregated into three groups: (i) a set of tat(-) viruses that have a functional HTLV-I Tax inserted in nef; (ii) a set of tat(-) viruses with Gal4 binding sites inserted in U3 and a Gal4-VP16 cDNA inserted in nef; and (iii) a set of tat(+) HIV genomes that are 5' and 3' TAR(-) and are Gal4-binding-site(+) in U3 and Gal4-VP16(+) in nef. We found that viruses in groups (i) and (ii), although tat(-), were fully complemented for viral gene expression based on quantitative measurements of viral protein synthesis and on the visualization by electron microscopy of the proper assembly of morphologically correct virions. Interestingly, group (i) and (ii) virions were defective in a spreading cytopathic infection when assayed in T-lymphocytes. Group (iii) viruses, although capable of producing intact Tat protein, also could not use Tat for transcription/gene expression because of the TAR(-) genotype. However, this class of viral genomes produced viruses that were highly infectious and cytopathic in primary and in continuously propagated T-lymphocytes. These three groups of viruses are all transcriptionally Tat-TAR independent. Their distinct differences in infectivity/cytopathicity provide genetic evidence that Tat provides a transcriptionally independent function in determining infectivity and cytopathicity in the setting of a spreading viral infection. Given that all HIV virions normally contain four intact copies of TAR RNA, our findings suggest a re-examination of whether Tat could be a virion-TAR-associated protein and the possible implications of this for virus infectivity/cytopathicity.
Subjects
Cytopathicity; HIV; TAT; Transcription regulation; Virus infectivity
SDGs

[SDGs]SDG3

Other Subjects
Tax protein; transactivator protein; article; gene expression; Human immunodeficiency virus 1; nonhuman; priority journal; provirus; T lymphocyte; transcription regulation; virion; virus gene; virus infectivity; virus mutant; HTLV; Human immunodeficiency virus; Human immunodeficiency virus 1; Human T-lymphotropic virus 1
Publisher
Wiley-VCH Verlag
Type
journal article

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