The kinetics of HIV-1 long terminal repeat transcriptional activation resemble those of hsp70 promoter in heat-shock treated HeLa cells

FEBS Letters ◽  
1994 ◽  
Vol 351 (2) ◽  
pp. 191-196 ◽  
Author(s):  
Carole Kretz-Remy ◽  
Andre-Patrick Arrigo
1988 ◽  
Vol 7 (10) ◽  
pp. 3143-3147 ◽  
Author(s):  
J. A. Garcia ◽  
D. Harrich ◽  
L. Pearson ◽  
R. Mitsuyasu ◽  
R. B. Gaynor

1996 ◽  
Vol 11 (3) ◽  
pp. 153-158 ◽  
Author(s):  
V. Zoumpourlis ◽  
M. Ergazaki ◽  
D.A. Spandidos

We employed a recombinant plasmid, pBHIV1, carrying the long terminal repeat (LTR) sequences of HIV-1 linked to the reporter chloramphenicol acetyl transferase (CAT) gene and to the aminoglycoside phosphotransferase (aph) gene as a selectable marker. We introduced pBHIV1 into human epithelial and fibroblast tumor cell lines (HeLa and MRCSV40TGR), and obtained stable geneticin-resistant HLHIV1-A and SVTGHIV1-A cells, respectively. The response to the retinoic acid was studied on the LTR regulated CAT activity in both cell lines. It was found that retinoic acid at a concentration of 1×10−5 effects a 3.2 - fold increase in CAT expression compared to HIV LTR in HLHIV1-A, but requires a concentration of 5×10−5 M to enhance this expression 4.6-fold in SVTGHIV1-A cells. These data show that retinoic acid may play a critical role in HIV-1 expression in human epithelial and fibroblast cell lines.


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