Hurford R K, Cobrinik D, Lee M H, Dyson N
Massachusetts General Hospital Cancer Center, Charlestown 02129, USA.
Genes Dev. 1997 Jun 1;11(11):1447-63. doi: 10.1101/gad.11.11.1447.
The activity of the E2F transcription factor is controlled by physical association with the retinoblastoma protein (pRB) and two related proteins, p107 and p130. The pRB family members are thought to control different aspects of E2F activity, but it has been unclear what the respective functions of these proteins might be. To dissect the specific functions of pRB, p107, and p130 we have investigated how the expression of E2F-regulated genes is changed in cultures of primary cells lacking each of these family members. Whereas no changes were found in the expression of E2F-target genes in cells lacking either p107 or p130, deregulated expression of E2F targets was seen in cells lacking pRB and in cells lacking both p107 and p130. Surprisingly, the genes that were disregulated in these two settings were completely different. These findings show that pRB and p107/p130 indeed provide different functions in E2F regulation and identify target genes that are dependent on pRB family proteins for their normal expression.
E2F转录因子的活性受与视网膜母细胞瘤蛋白(pRB)以及两种相关蛋白p107和p130的物理结合控制。pRB家族成员被认为控制E2F活性的不同方面,但这些蛋白各自的功能尚不清楚。为了剖析pRB、p107和p130的具体功能,我们研究了在缺乏这些家族成员之一的原代细胞培养物中,E2F调控基因的表达是如何变化的。在缺乏p107或p130的细胞中,未发现E2F靶基因的表达有变化,而在缺乏pRB的细胞以及同时缺乏p107和p130的细胞中,可见E2F靶标的表达失调。令人惊讶的是,在这两种情况下失调的基因完全不同。这些发现表明,pRB和p107/p130在E2F调控中确实发挥不同功能,并鉴定出其正常表达依赖于pRB家族蛋白的靶基因。