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Inactivation of the Human Immunodeficiency Virus Type 1 Inhibitory Elements Allows Rev-Independent Expression of Gag and Gag/Protease and Particle Formation

  1. Author:
    Schneider, R.
    Campbell, M.
    Nasioulas, G.
    Felber, B. K.
    Pavlakis, G. N.
  2. Author Address

    Pavlakis GN NCI FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM HUMAN RETROVIRUS SECT BLDG 535 RM 210 FREDERICK, MD 21703 USA NCI FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM HUMAN RETROVIRUS SECT FREDERICK, MD 21703 USA NCI FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM HUMAN RETROVIRUS PATHOGENESIS GRP FREDERICK, MD 21703 USA
    1. Year: 1997
  1. Journal: Journal of Virology
    1. 71
    2. 7
    3. Pages: 4892-4903
  2. Type of Article: Article
  1. Abstract:

    The expression of gag, pol, and env of human immunodeficiency virus type 1 (HIV-1) depends on the presence of the viral Rev protein, This dependence is, at least in part, due to the presence of negatively acting sequences (inhibitory or instability elements [INS]) located within unspliced and partially spliced mRNAs, The positive interaction of Rev with the Rev-responsive element in these mRNAs counteracts the negative effects of the inhibitory sequences, Here, we demonstrate that in addition to the previously identified INS1 within p17(gag), several other INS elements exist within the gag/pol region of HIV-1 These elements act independently of each other and were eliminated by mutagenesis after the introduction of multiple paint mutations not affecting the coding region, leading to constitutive high levels of Gag expression, Expression vectors containing an intact or nearly intact p55(gag) region allowed the production of immature viral particles in mammalian cells in the absence of any other HN proteins, The introduction of additional mutations in the protease region allowed efficient production of Gag/protease, which resulted in processing of the Pr55(gag) precursor and production of mature Gag particles with a lentivirus-like conical-core structure, The elimination of a newly identified INS clement within pol and the previously identified CRS located within int was accomplished by tile same methodology, Sequence comparisons of the identified inhibitory elements revealed no apparent homologies and demonstrated that these sequences are not splice sites, These results demonstrate that the elimination of INS elements leads to efficient expression of HIV-1 mRNAs in the absence of Rev or any posttranscriptional activating mechanisms. [References: 39]

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