Studies on the down-regulation of major histocompatibility complex class I gene expression in adenovirus-transformed cells

1997 ◽  
Vol 25 (2) ◽  
pp. 352S-352S ◽  
Author(s):  
NICOLA J. PHILPOTT ◽  
JAMES A. PROFFITT ◽  
G. ERIC BLAIR
1996 ◽  
Vol 16 (1) ◽  
pp. 398-404 ◽  
Author(s):  
X Liu ◽  
R Ge ◽  
R P Ricciardi

Diminished expression of major histocompatibility complex class I antigens on the surface of adenovirus type 12 (Ad12)-transformed cells contributes to their high tumorigenic potential by enabling them to escape immune recognition by cytotoxic T lymphocytes. This low class I antigen expression is due to a block in class I transcription, which is mediated by Ad12 E1A. Genetic analysis has shown that the class I enhancer is the target for transcriptional down-regulation. In this study, we show that the ability of the R1 element of the class I enhancer to stimulate transcription is greatly reduced in Ad12-transformed cells. The loss of functional activity by the R1 element was attributed to loss of binding by the NF-kappa B p50-p65 heterodimer. NF-kappa B binding appears to be blocked within the nucleus rather than at the level of nuclear translocation. Significantly, NF-kappa B binding activity could be recovered from the nuclear extracts of Ad12-transformed cells following detergent treatment, suggesting that the block is mediated through a nuclear inhibitor present in the Ad12-transformed cells. These results, taken together with the fact that the R2 element of the class I enhancer exhibits strong binding to the transcriptional repressor COUP-TF, suggest that the class I enhancer is globally down-regulated in Ad12-transformed cells.


2009 ◽  
Vol 82 (1) ◽  
pp. 48-56 ◽  
Author(s):  
Julie Doyle ◽  
Shirley A. Ellis ◽  
Grace M. O’Gorman ◽  
Ines Maria Aparicio Donoso ◽  
Patrick Lonergan ◽  
...  

1997 ◽  
Vol 272 (32) ◽  
pp. 20096-20107 ◽  
Author(s):  
Motoyasu Saji ◽  
Minho Shong ◽  
Giorgio Napolitano ◽  
Lisa A. Palmer ◽  
Shin-Ichi Taniguchi ◽  
...  

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