TRANSCRIPTIONAL CONTROL OF THE HTF9-A/RANBP-1 GENE DURING THE CELL-CYCLE

被引:0
|
作者
DIMATTEO, G
FUSCHI, P
ZERFASS, K
MORETTI, S
RICORDY, R
CENCIARELLI, C
TRIPODI, M
JANSENDURR, P
LAVIA, P
机构
[1] UNIV ROMA LA SAPIENZA,DEPT GENET & MOLEC BIOL,CTR EVOLUT GENET,CNR,I-00185 ROME,ITALY
[2] DEUTSCH KREBSFORSCHUNGSZENTRUM,D-69120 HEIDELBERG,GERMANY
[3] CNR,INST BIOMED TECHNOL,I-00158 ROME,ITALY
[4] UNIV ROMA LA SAPIENZA,DEPT HUMAN BIOPATHOL,CELLULAR BIOL SECT,I-00185 ROME,ITALY
来源
CELL GROWTH & DIFFERENTIATION | 1995年 / 6卷 / 10期
关键词
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中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mouse Htf9-a gene encodes a small hydrophilic protein, named Ran-binding protein 1 (RanBP-1), for its interaction with the Ras-related Ran protein; RanBP-1 binds the biologically active form of Ran. Ran has been implicated in a variety of nuclear events including DNA replication, RNA export and protein import, and monitoring completion of DNA synthesis before the onset of mitosis; its biological activity is thought to be regulated in S phase. We have investigated whether expression of the Htf9-a/RanBP-1 gene is linked to cell proliferation. Expression of the Htf9-a/RanBP-1 transcript appeared to be dependent on the proliferating state of the cells and peaked in S phase. We have identified a promoter region required for Htf9-a cell cycle-dependent expression and for responsiveness to cell cycle regulators. An E2F-binding site was identified within the cell cycle-regulated promoter region. Expression of the E1A oncoprotein prevented Htf9-a down-regulation in quiescent cells; in addition, both pRb and its relative p107 inhibited transcription from the Htf9-a promoter. These results link the control of Htf9a/RanBP-1 expression to the cell cycle progression.
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页码:1213 / 1224
页数:12
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