Literature DB >> 2995968

Location of cis-acting regulatory sequences in the human T-cell leukemia virus type I long terminal repeat.

C A Rosen, J G Sodroski, W A Haseltine.   

Abstract

The location of cis-acting regulatory regions within the long terminal repeat (LTR) of the human T-cell leukemia virus type I (HTLV-1) was determined. The sequences present between nucleotides -350 and -55 (cap site +1) contain an enhancer element that is active in lymphoid and nonlymphoid cell lines. The sequences located near the "TATA" and RNA initiation sites contain a promoter, the activity of which can be augmented by homologous and heterologous enhancer elements. A region responsive to trans-acting transcription factors present in HTLV-I- and HTLV type II-infected cells is located between nucleotides -159 and +315. HTLV-I LTR deletion mutants respond in a similar manner both to the trans-acting factors present in infected cells and to the tat protein encoded by the x-lor region of the genome, thus providing further evidence that the tat protein mediates transcriptional trans-activation of the LTR in HTLV-infected cells.

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Year:  1985        PMID: 2995968      PMCID: PMC390745          DOI: 10.1073/pnas.82.19.6502

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  43 in total

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4.  Analysis of transcriptional regulatory signals of the HSV thymidine kinase gene: identification of an upstream control region.

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5.  Host-specific activation of transcription by tandem repeats from simian virus 40 and Moloney murine sarcoma virus.

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Authors:  C M Gorman; G T Merlino; M C Willingham; I Pastan; B H Howard
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10.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.

Authors:  J M Chirgwin; A E Przybyla; R J MacDonald; W J Rutter
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  52 in total

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7.  Transcriptional suppression of the human T-cell leukemia virus type I long terminal repeat occurs by an unconventional interaction of a CREB factor with the R region.

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8.  Defibrinated bovine plasma inhibits retroviral transcription by blocking p52 activation of the NFkappaB element in the long terminal repeat.

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10.  Identification of human T-cell lymphotropic virus type I 21-base-pair repeat-specific and glial cell-specific DNA-protein complexes.

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