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Identification of an Rna Sequence Within an Intracisternal-a Particle Element Able to Replace Rev-Mediated Posttranscriptional Regulation of Human Immunodeficiency Virus Type 1

  1. Author:
    Tabernero, C.
    Zolotukhin, A. S.
    Bear, J.
    Schneider, R.
    Karsenty, G.
    Felber, B. K.
  2. Author Address

    Felber BK NCI HUMAN RETROVIRUS PATHOGENESIS GRP FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM FREDERICK, MD 21702 USA NCI HUMAN RETROVIRUS PATHOGENESIS GRP FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM FREDERICK, MD 21702 USA NCI HUMAN RETROVIRUS SECT FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM FREDERICK, MD 21702 USA UNIV TEXAS MD ANDERSON CANCER CTR DEPT MOL GENET HOUSTON, TX 77030 USA
    1. Year: 1997
  1. Journal: Journal of Virology
    1. 71
    2. 1
    3. Pages: 95-101
  2. Type of Article: Article
  1. Abstract:

    Human immunodeficiency virus type 1 (HIV-1) replication depends on the posttranscriptional regulation by the viral Rev protein and can be replaced with the posttranscriptional RNA control element (CTE) of the type D simian retroviruses. We have identified a sequence which shares only nucleotide sequences of the internal loops and secondary structure with the CTE and which is part of a novel murine intracisternal-A particle (IAP) retroelement, inserted within the transcribed mouse osteocalcin-related gene. This sequence, named CTE(IAP), can replace the Rev-mediated regulation of HIV-1, hence it is a posttranscriptional regulatory element, Related elements have been identified in other IAPs. These results suggest that insertional mutagenesis can affect gene expression by providing a functional posttranscriptional control element. The CTE(IAP) and CTEs of the type D simian retroviruses represent a novel class of RNA elements characterized by unique sequences within the internal loops which are predicted to represent the interaction site,vith cellular factor(s). These findings suggest that such elements may be involved in posttranscriptional regulation of cellular mRNAs. [References: 48]

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