Tandem AP-1-binding sites within the human beta-globin dominant control region function as an inducible enhancer in erythroid cells.
Open Access
- 1 June 1990
- journal article
- research article
- Published by Cold Spring Harbor Laboratory in Genes & Development
- Vol. 4 (6) , 993-1006
- https://doi.org/10.1101/gad.4.6.993
Abstract
A powerful enhancer has been mapped to an 18-bp DNA segment located 11 kb 5' to the human epsilon-globin gene within the dominant control or locus-activating region. This enhancer is inducible in K562 human erythroleukemia cells, increasing linked gamma-globin promoter/luciferase gene expression to 170-fold over an enhancerless construct. The enhancer consists of tandem AP-1-binding sites, phased 10 bp apart, which are both required for full activity. DNA-protein binding assays with nuclear extracts from induced cells demonstrate a high molecular weight complex on the enhancer. The formation of this complex also requires both AP-1 sites and correlates with maximal enhancer activity. Induction of the enhancer may have a role in the increase in globin gene transcription that characterizes erythroid maturation. Enhancer activity appears to be mediated by the binding of a complex of proteins from the jun and fos families to tandem AP-1 consensus sequences.This publication has 90 references indexed in Scilit:
- Developmental modulation of protein binding to beta-globin gene regulatory sites within chicken erythrocyte nuclei.Genes & Development, 1989
- Fos and jun: The AP-1 connectionCell, 1988
- Position-independent, high-level expression of the human β-globin gene in transgenic miceCell, 1987
- Activation of the human beta-globin promoter in K562 cells by DNA sequences 5' to the fetal gamma- or embryonic zeta-globin genes.Journal of Clinical Investigation, 1987
- Developmental regulation of a cloned adult β-globin gene in transgenic miceNature, 1985
- Expression of red cell antigens by K562 human leukemia cells before and after induction of hemoglobin synthesis by heminTransfusion, 1985
- Regulated expression of the human β-globin gene family in murine erythroleukaemia cellsNature, 1983
- The regulated expression of β-globin genes introduced into mouse erythroleukemia cellsCell, 1983
- Biochemical transfer of single-copy eucaryotic genes using total cellular DNA as donorCell, 1978
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976