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Molecular and Cellular Biology, May 2008, p. 3101-3113, Vol. 28, No. 10
0270-7306/08/$08.00+0     doi:10.1128/MCB.01858-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Silencing of A{gamma}-Globin Gene Expression during Adult Definitive Erythropoiesis Mediated by GATA-1-FOG-1-Mi2 Complex Binding at the –566 GATA Site{triangledown} ,{dagger}

Susanna Harju-Baker,1,§,{ddagger} Flávia C. Costa,1,{ddagger} Halyna Fedosyuk,1 Renee Neades,1 and Kenneth R. Peterson1,2*

Departments of Biochemistry and Molecular Biology,1 Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas 661602

Received 11 October 2007/ Returned for modification 20 November 2007/ Accepted 8 March 2008

Autonomous silencing of {gamma}-globin transcription is an important developmental regulatory mechanism controlling globin gene switching. An adult stage-specific silencer of the A{gamma}-globin gene was identified between –730 and –378 relative to the mRNA start site. A marked copy of the A{gamma}-globin gene inserted between locus control region 5' DNase I-hypersensitive site 1 and the {varepsilon}-globin gene was transcriptionally silenced in adult β-globin locus yeast artificial chromosome (β-YAC) transgenic mice, but deletion of the 352-bp region restored expression. This fragment reduced reporter gene expression in K562 cells, and GATA-1 was shown to bind within this sequence at the –566 GATA site. Further, the Mi2 protein, a component of the NuRD complex, was observed in erythroid cells with low {gamma}-globin levels, whereas only a weak signal was detected when {gamma}-globin was expressed. Chromatin immunoprecipitation of fetal liver tissue from β-YAC transgenic mice demonstrated that GATA-1, FOG-1, and Mi2 were recruited to the A{gamma}-globin –566 or G{gamma}-globin –567 GATA site when {gamma}-globin expression was low (day 18) but not when {gamma}-globin was expressed (day 12). These data suggest that during definitive erythropoiesis, {gamma}-globin gene expression is silenced, in part, by binding a protein complex containing GATA-1, FOG-1, and Mi2 at the –566/–567 GATA sites of the proximal {gamma}-globin promoters.


* Corresponding author. Mailing address: Department of Biochemistry and Molecular Biology, MS 3030, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160. Phone: (913) 588-6907. Fax: (913) 588-7440. E-mail: kpeterson{at}kumc.edu

{triangledown} Published ahead of print on 17 March 2008.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.

§ Present address: Center for Lung Biology, University of Washington School of Medicine, Seattle, WA 98109.

{ddagger} Co-first authors: these authors contributed equally to this work.


Molecular and Cellular Biology, May 2008, p. 3101-3113, Vol. 28, No. 10
0270-7306/08/$08.00+0     doi:10.1128/MCB.01858-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.




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