The expression of aldolase A L-type mRNA is increased in growth-arrested mouse NIH3T3 cells and remarkably down-regulated in actively proliferating cells. Treatment of proliferating cells with cycloheximide abolished the down-regulation of L-type mRNA expression, thus indicating that a protein factor acts as repressor in proliferating cells. Transient transfection experiments in NIH3T3 cells showed that a negative regulatory cis-element (NRE) is involved in the modulation of the transcriptional activity of the distal L promoter. The repressor, which is a protein of ~97 kDa, binds the murine aldolase A NRE, revealing a much more intense DNA-protein complex in proliferating NIH3T3 cells than in serum-deprived cells. Mutations in the negative regulatory cis-element showed that the GA-rich motif is required for protein binding and silencer function. We conclude that the expression of L- type mRNA is modulated by the interaction between a cell cycle-dependent DNA- binding protein and the murine aldolase A NRE.
Negative regulation of the mouse aldolase A gene: A cell cycle-dependent DNA binding activity functions as a silencer of gene transcription / Lupo, A.; Costanzo, Paola; Medugno, L.; Romeo, I.; Salvatore, F.; Izzo, P.. - In: THE JOURNAL OF BIOLOGICAL CHEMISTRY. - ISSN 0021-9258. - 272:50(1997), pp. 31641-31647. [10.1074/jbc.272.50.31641]
Negative regulation of the mouse aldolase A gene: A cell cycle-dependent DNA binding activity functions as a silencer of gene transcription
COSTANZO, PAOLA;
1997
Abstract
The expression of aldolase A L-type mRNA is increased in growth-arrested mouse NIH3T3 cells and remarkably down-regulated in actively proliferating cells. Treatment of proliferating cells with cycloheximide abolished the down-regulation of L-type mRNA expression, thus indicating that a protein factor acts as repressor in proliferating cells. Transient transfection experiments in NIH3T3 cells showed that a negative regulatory cis-element (NRE) is involved in the modulation of the transcriptional activity of the distal L promoter. The repressor, which is a protein of ~97 kDa, binds the murine aldolase A NRE, revealing a much more intense DNA-protein complex in proliferating NIH3T3 cells than in serum-deprived cells. Mutations in the negative regulatory cis-element showed that the GA-rich motif is required for protein binding and silencer function. We conclude that the expression of L- type mRNA is modulated by the interaction between a cell cycle-dependent DNA- binding protein and the murine aldolase A NRE.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.