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. 1986 Apr;5(4):713-8.
doi: 10.1002/j.1460-2075.1986.tb04272.x.

A transcriptional enhancer sequence of HTLV-I is responsible for trans-activation mediated by p40 chi HTLV-I

A transcriptional enhancer sequence of HTLV-I is responsible for trans-activation mediated by p40 chi HTLV-I

J Fujisawa et al. EMBO J. 1986 Apr.

Abstract

Human T-cell leukemia virus type I (HTLV-I) contains a unique sequence pX that is located between env and the 3' long terminal repeat (LTR) and codes for three pX proteins, p40 chi, pp27 chi-III and pp21 chi-III. One of these proteins, p40 chi, was previously shown to activate transcription from the LTR in a trans-acting manner, which suggested that it activated some cellular genes involved in leukemogenesis. In this study, the sequences in the LTR responsible for this trans-activation were analyzed. Construction of deletion mutants of the LTR in pLTR-CAT and measurement of their activities in trans-activated expression of the CAT gene showed that sequences upstream of the TATA box were responsible for the trans-activation mediated by p40 chi. The active unit was identified as an enhancer sequence containing direct repeats by inserting it into an enhancer-minus SV40 promoter. Thus, it was concluded that an enhancer sequence in HTLV-I LTR is responsible, at least in part, for transcriptional trans-activation mediated by the viral product p40 chi.

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    1. Science. 1985 Jun 28;228(4707):1532-4 - PubMed
    1. Science. 1985 Jun 21;228(4706):1430-4 - PubMed
    1. Science. 1985 Jul 5;229(4708):54-8 - PubMed
    1. Science. 1985 Aug 16;229(4714):675-9 - PubMed
    1. Proc Natl Acad Sci U S A. 1985 Oct;82(19):6502-6 - PubMed

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