Cloning of the mouse BTG3 gene and definition of a new gene family (the BTG family) involved in the negative control of the cell cycle

被引:104
作者
Guehenneux, F
Duret, L
Callanan, M
Bouhas, R
Hayette, S
Berthet, C
Samarut, C
Rimokh, R
Birot, AM
Wang, Q
Magaud, JP
Rouault, JP
机构
[1] CTR LEON BERARD,CNRS,INSERM,UNITE 453,F-69373 LYON 08,FRANCE
[2] CTR LEON BERARD,UNITE ONCOL MOL,F-69373 LYON 08,FRANCE
[3] UCLB,CNR,UMR 5558,LAB BGBP,VILLEURBANNE,FRANCE
[4] INST A BONNIOT,GRP RECH LYMPHOMES,LA TRONCHE,FRANCE
[5] HOP EDOUARD HERRIOT,LAB CYTOGENET & CYTOGENET MOL,LYON,FRANCE
关键词
BTG; 1; 2; 3; PC3; TIS21; TOB; antiproliferative gene;
D O I
10.1038/sj.leu.2400599
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is well known that loss of tumor suppressor genes and more generally of antiproliferative genes plays a key role in the development of most tumors. We report here the cloning of the mouse BTG3 gene and show that its human counterpart maps on chromosome 21. This evolutionarily conserved gene codes for a 30 kDa protein and is expressed in most adult murine and human tissues analyzed. However, we demonstrate that its expression is cell cycle dependent and peaks at the end of the G(1) phase. This gene is homologous to the human BTG1, BTG2 and TOB genes which were demonstrated to act as inhibitors of cell proliferation. Its description allowed us to define better this seven gene family (the BTG gene family) at the structural level and to speculate about its physiological role in normal and tumoral cells. This family is mainly characterized by the presence of two conserved domains (BTG boxes A and B) of as yet undetermined function which are separated by a nonconserved 20-25 amino acid sequence.
引用
收藏
页码:370 / 375
页数:6
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