Horstmann S, Ferrari S, Klempnauer K H
Institute of Biochemistry, University of Münster, Wilhelm-Klemm-Str. 2, D-48149 Münster, Germany.
Oncogene. 2000 Jan 13;19(2):298-306. doi: 10.1038/sj.onc.1203302.
Evidence obtained during recent years suggests that B-Myb, a highly conserved member of the Myb transcription factor family, plays a key role in cell proliferation. We have shown previously that the activity of B-Myb is stimulated by cyclin A/Cdk2-dependent phosphorylation of the carboxyl-terminus of B-Myb. We have now investigated in more detail the effect of other cyclins on B-Myb. Here, we show that cyclin D1, in contrast to cyclin A, strongly inhibits the activity of B-Myb. This inhibitory effect does not involve increased phosphorylation of B-Myb but seems to rely on the formation of a specific complex of B-Myb and cyclin D1. Our work identifies B-Myb as an interacting partner for cyclin D1 and suggest that the activity of B-Myb during the cell cycle is controlled by the antagonistic effects of cyclin D1 and A. The results presented here suggest a more general role of cyclin D1 as regulator of transcription in addition to the known effect on RB phosphorylation.
近年来获得的证据表明,B-Myb是Myb转录因子家族中高度保守的成员,在细胞增殖中起关键作用。我们之前已经表明,B-Myb的活性受到细胞周期蛋白A/Cdk2介导的B-Myb羧基末端磷酸化的刺激。我们现在更详细地研究了其他细胞周期蛋白对B-Myb的影响。在此,我们表明,与细胞周期蛋白A相反,细胞周期蛋白D1强烈抑制B-Myb的活性。这种抑制作用并不涉及B-Myb磷酸化的增加,而是似乎依赖于B-Myb与细胞周期蛋白D1特异性复合物的形成。我们的工作确定B-Myb是细胞周期蛋白D1的相互作用伴侣,并表明细胞周期蛋白D1和A的拮抗作用控制了细胞周期中B-Myb的活性。此处给出的结果表明,除了对RB磷酸化的已知作用外,细胞周期蛋白D1作为转录调节因子具有更广泛的作用。