SRα Promoter: an Efficient and Versatile Mammalian cDNA Expression System Composed of the Simian Virus 40 Early Promoter and the R-U5 Segment of Human T-Cell Leukemia Virus Type 1 Long Terminal Repeat

Yutaka Takebe(Cellular Research (United States)), Motoharu Seiki(The Cancer Institute Hospital), Jun–ichi Fujisawa(The Cancer Institute Hospital), P Hoy(Cellular Research (United States)), Kyoko Yokota(Cellular Research (United States)), Ken‐ichi Arai(Cellular Research (United States)), Mitsuaki Yoshida(The Cancer Institute Hospital), Naoko Arai(Cellular Research (United States))
Molecular and Cellular Biology
January 1, 1988
Cited by 1,336Open Access
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Abstract

We developed a novel promoter system, designated SR alpha, which is composed of the simian virus 40 (SV40) early promoter and the R segment and part of the U5 sequence (R-U5') of the long terminal repeat of human T-cell leukemia virus type 1. The R-U5' sequence stimulated chloramphenicol acetyltransferase (CAT) gene expression only when placed immediately downstream of the SV40 early promoter in the sense orientation. The SR alpha expression system was 1 or 2 orders of magnitude more active than the SV40 early promoter in a wide variety of cell types, including fibroblasts and lymphoid cells, and was capable of promoting a high level of expression of various lymphokine cDNAs. These features of the SR alpha promoter were incorporated into the pcD-cDNA expression cloning vector originally developed by Okayama and Berg.


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