REGULATION OF TRANSFORMING GROWTH FACTOR-BETA-1 GENE-EXPRESSION BY THE PRODUCT OF THE RETINOBLASTOMA-SUSCEPTIBILITY GENE

被引:178
作者
KIM, SJ [1 ]
LEE, HD [1 ]
ROBBINS, PD [1 ]
BUSAM, K [1 ]
SPORN, MB [1 ]
机构
[1] UNIV PITTSBURGH,SCH MED,DEPT MOLEC GENET & BIOCHEM,PITTSBURGH,PA 15261
关键词
PROMOTER; RETINOBLASTOMA RESPONSE ELEMENT; TUMOR SUPPRESSOR; GROWTH FACTOR;
D O I
10.1073/pnas.88.8.3052
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transforming growth factor-beta (TGF-beta) isoforms inhibit the growth of many cell types and block progression of the cell cycle by inhibiting events in late G1 phase. The retinoblastoma gene product, RB, also has properties of a cell-cycle regulatory factor. It remains underphosphorylated in the presence of TGF-beta and has been shown to repress the activity of the c-fos promoter, resulting in inhibition of transit through the cell cycle. These observations led us to examine effects of human RB on the expression of the human TGF-beta-1 gene. Using chimeric TGF-beta-1 promoter-chloramphenicol acetyltransferase gene constructs, we show that RB induces TGF-beta-1 gene expression in CCL-64 mink lung epithelial cells and A-549 human lung adenocarcinoma cells but represses its expression in NIH 3T3 and AKR-2B mouse cells. Several sequences homologous to the c-fos RB control element were identified in the TGF-beta-1 promoter. These results demonstrate that human RB can regulate TGF-beta-1 gene expression negatively or positively depending on the cell type.
引用
收藏
页码:3052 / 3056
页数:5
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