INDIVIDUAL STAGE SELECTOR ELEMENT MUTATIONS LEAD TO RECIPROCAL CHANGES IN BETA-GLOBIN VS EPSILON-GLOBIN GENE-TRANSCRIPTION - GENETIC CONFIRMATION OF PROMOTER COMPETITION DURING GLOBIN GENE SWITCHING

被引:100
作者
FOLEY, KP
ENGEL, JD
机构
[1] Department of Biochemistry, Northwestern University, Evanston
关键词
GLOBIN GENE SWITCHING; POLYMERASE CHAIN REACTION; PROMOTER COMPETITION; TRANSCRIPTION FACTORS;
D O I
10.1101/gad.6.5.730
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Biochemical and genetic analysis of the embryonic to adult beta-like globin gene switch in chickens has led to the hypothesis that competition between the promoters of the cis-linked epsilon- and beta-globin genes for interaction with a shared enhancer mediates the developmental changes in expression of beta-globin protein isotypes. To test specific predictions of this promoter competition model, a sensitive RNA/polymerase chain reaction assay has been used to investigate the effects of individual beta-globin promoter mutations on expression of the two linked genes in transiently transfected erythroid cells. Mutations that attenuated adult beta-globin transcription resulted concomitantly in a proportional increase in expression of the embryonic epsilon-globin gene. Consistent with the model, mutations disrupting the binding sites for either of two adult stage-specific transcription factors (NF-E4 and beta-CTF) indicate that these sites are essential both for induction of beta-globin gene expression and for indirect suppression (through promoter competition) of epsilon-globin transcription in definitive (adult) erythroid cells. These results provide direct evidence that stage-specific transcription factors affect the equilibrium existing between multiple interacting globin cis-regulatory elements. We conclude that promoter competition is an important mechanism through which developmental regulation of chicken beta-globin gene switching is achieved and that such competitive interactions may prove to be generally applicable to the regulation of a variety of other temporally or spatially restricted gene expression patterns.
引用
收藏
页码:730 / 744
页数:15
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