Duriez Cyril, Moyret-Lalle Caroline, Falette Nicole, El-Ghissassi Fatiha, Puisieux Alain
INSERM U453, Unité d'Oncologie Moléculaire, Centre Léon Bérard, 28 rue Laënnec, 69008 Lyon, FRANCE.
Bull Cancer. 2004 Jul-Aug;91(7-8):E242-53.
The human BTG2 gene is one of five members of a newly identified family of antiproliferative genes. BTG2 was first described as an immediate early gene whose expression is induced in response to mitogenic as well as differentiative and antiproliferative factors. More recently, we have shown that BTG2 expression is also induced in response to genotoxic stress through a p53-dependent mechanism. Experimental overexpression of the BTG2 gene in NIH3T3 and PC12 cells leads to a partial inhibition of cell proliferation. BTG2 protein physically interacts with Caf1 protein, an element of a general transcription complex, and with PRMT1, a protein-arginine N-methyl transferase. We speculate on the role of BTG2 as a modulator of the intracellular signal transduction cascade.
人类BTG2基因是新发现的抗增殖基因家族的五个成员之一。BTG2最初被描述为一种即时早期基因,其表达可因促有丝分裂因子以及分化和抗增殖因子而被诱导。最近,我们已经表明,BTG2的表达也可通过p53依赖性机制因基因毒性应激而被诱导。在NIH3T3和PC12细胞中实验性过表达BTG2基因会导致细胞增殖受到部分抑制。BTG2蛋白与Caf1蛋白(一种通用转录复合体的元件)以及PRMT1(一种蛋白质精氨酸N-甲基转移酶)发生物理相互作用。我们推测BTG2作为细胞内信号转导级联反应的调节因子所起的作用。