Engel J D
Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208-3500.
Trends Genet. 1993 Sep;9(9):304-9. doi: 10.1016/0168-9525(93)90248-g.
Synthesis of different hemoglobin polypeptides during the early stages of human development is principally regulated by transcriptional control mechanisms that determine which of the five beta-type globin genes is expressed. The means by which this is achieved have been scrutinized for several decades, and insights have been gained from introducing segments of the human beta-globin locus into transgenic mice, and from analysis of naturally occurring mutations at the locus. I describe here a model which attempts to resolve several of the current puzzles and provides simple, testable predictions for how differential beta-globin gene transcription might be achieved during human development.
在人类发育早期不同血红蛋白多肽的合成主要受转录控制机制调节,该机制决定五个β型珠蛋白基因中的哪一个被表达。几十年来,人们一直在仔细研究实现这一过程的方式,并且通过将人类β-珠蛋白基因座的片段导入转基因小鼠以及对该基因座自然发生的突变进行分析获得了一些见解。我在此描述一个模型,该模型试图解决当前的几个难题,并为人类发育过程中如何实现β-珠蛋白基因的差异转录提供简单且可检验的预测。