Dillon N, Trimborn T, Strouboulis J, Fraser P, Grosveld F
MRC Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London, United Kingdom.
Mol Cell. 1997 Dec;1(1):131-9. doi: 10.1016/s1097-2765(00)80014-3.
We have used gene competition to distinguish between possible mechanisms of transcriptional activation of the genes of the human beta-globin locus. The insertion of a second beta-globin gene at different points in the locus shows that the more proximal beta gene competes more effectively for activation by the locus control region (LCR). Reducing the relative distance between the genes and the LCR reduces the competitive advantage of the proximal gene, a result that supports activation by direct interaction between the LCR and the genes. Visualization of the primary transcripts shows that the level of transcription is proportional to the frequency of transcriptional periods and that such periods last approximately 8 min in vivo. We also find that the position of the beta-globin gene in the locus is important for correct developmental regulation.
我们利用基因竞争来区分人类β-珠蛋白基因座基因转录激活的可能机制。在该基因座的不同位置插入第二个β-珠蛋白基因表明,位置更靠近(基因座控制区)LCR的β基因在竞争LCR激活时更有效。缩短基因与LCR之间的相对距离会降低近端基因的竞争优势,这一结果支持了LCR与基因之间直接相互作用导致的激活。初级转录本的可视化显示,转录水平与转录周期的频率成正比,并且在体内这种周期持续约8分钟。我们还发现β-珠蛋白基因在基因座中的位置对于正确的发育调控很重要。