Grosveld F, de Boer E, Dillon N, Fraser P, Gribnau J, Milot E, Trimborn T, Wijgerde M
MGC-Department of Cell Biology and Genetics, Erasmus University, The Netherlands.
Semin Hematol. 1998 Apr;35(2):105-11.
The most important level of the regulation of the beta-globin genes is by activation of all of the genes by the locus control region (LCR). Part of the developmental regulation of the locus is achieved by competition of the genes for the interaction with the LCR. Although this level of gene regulation is quantitatively of less importance than the direct repression mechanism for the early genes, it has important implications and has provided an excellent assay to probe the regulation of transcription at the single cell level. The results of these studies indicate that the LCR interacts with individual globin genes and that LCR/gene interactions are dynamic with complexes forming and dissociating continually. We conclude that transcription only appears to take place while the LCR and gene interact and that the level of transcription is determined by the frequency and duration of such interaction rather than by changes in the rate of transcription of the promoters. This mechanism has clear implications for the design of vectors for the purpose of gene therapy.
β-珠蛋白基因调控的最重要水平是由基因座控制区(LCR)激活所有基因。该基因座发育调控的一部分是通过基因竞争与LCR相互作用来实现的。尽管这种基因调控水平在数量上不如早期基因的直接抑制机制重要,但它具有重要意义,并为在单细胞水平探究转录调控提供了出色的检测方法。这些研究结果表明,LCR与单个珠蛋白基因相互作用,且LCR/基因相互作用是动态的,复合物不断形成和解离。我们得出结论,转录似乎仅在LCR与基因相互作用时发生,转录水平由这种相互作用的频率和持续时间决定,而非由启动子转录速率的变化决定。这种机制对用于基因治疗的载体设计具有明确的启示。