Department of Pediatrics, Center for Pediatric Biomedical Research, University of Rochester Medical Center, Rochester, NY 14642, USA.
Biochem Cell Biol. 2009 Oct;87(5):781-90. doi: 10.1139/O09-048.
The beta-globin gene cluster in mammals, consisting of a set of erythroid-specific, developmentally activated, and (or) silenced genes, has long presented a model system for the investigation of gene regulation. As the number and complexity of models of gene activation and repression have expanded, so too has the complexity of phenomena associated with the regulation of the beta-globin genes. Models for expression from within the locus must account for local (promoter-proximal), distal (enhancer-mediated), and domain-wide components of the regulatory pathways that proceed through mammalian development and erythroid differentiation. In this review, we provide an overview of transcriptional activation, silencing, chromatin structure, and the function of distal regulatory elements involved in the normal developmental regulation of beta-globin gene expression.
哺乳动物的β-珠蛋白基因簇由一组红细胞特异性、发育激活和(或)沉默的基因组成,长期以来一直是研究基因调控的模型系统。随着基因激活和抑制模型的数量和复杂性的增加,与β-珠蛋白基因调控相关的现象也变得更加复杂。来自基因座内的表达模型必须考虑通过哺乳动物发育和红细胞分化的调控途径的局部(启动子近端)、远端(增强子介导)和全域组成部分。在这篇综述中,我们概述了参与β-珠蛋白基因表达正常发育调控的转录激活、沉默、染色质结构和远端调节元件的功能。