Differential regulation of the α-globin locus by Krüppel-like factor 3 in erythroid and non-erythroid cells.

Autor: Funnell, Alister P. W., Vernimmen, Douglas, Lim, Wooi F., Mak, Ka Sin, Wienert, Beeke, Martyn, Gabriella E., Artuz, Crisbel M., Burdach, Jon, Quinlan, Kate G. R., Higgs, Douglas R., Whitelaw, Emma, Pearson, Richard C. M., Crossley, Merlin
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Zdroj: BMC Molecular Biology; 2014, Vol. 15 Issue 1, p2-23, 22p, 1 Black and White Photograph, 5 Graphs
Abstrakt: Background Krüppel-like Factor 3 (KLF3) is a broadly expressed zinc-finger transcriptional repressor with diverse biological roles. During erythropoiesis, KLF3 acts as a feedback repressor of a set of genes that are activated by Krüppel-like Factor 1 (KLF1). Noting that KLF1 binds α- globin gene regulatory sequences during erythroid maturation, we sought to determine whether KLF3 also interacts with the α-globin locus to regulate transcription. Results We found that expression of a human transgenic α-globin reporter gene is markedly upregulated in fetal and adult erythroid cells of Klf3-/- mice. Inspection of the mouse and human α-globin promoters revealed a number of canonical KLF-binding sites, and indeed, KLF3 was shown to bind to these regions both in vitro and in vivo. Despite these observations, we did not detect an increase in endogenous murine α-globin expression in Klf3-/- erythroid tissue. However, examination of murine embryonic fibroblasts lacking KLF3 revealed significant de-repression of α-globin gene expression. This suggests that KLF3 may contribute to the silencing of the α-globin locus in non-erythroid tissue. Moreover, ChIP-Seq analysis of murine fibroblasts demonstrated that across the locus, KLF3 does not occupy the promoter regions of the α-globin genes in these cells, but rather, binds to upstream, DNase hypersensitive regulatory regions. Conclusions These findings reveal that the occupancy profile of KLF3 at the α-globin locus differs in erythroid and non-erythroid cells. In erythroid cells, KLF3 primarily binds to the promoters of the adult α-globin genes, but appears dispensable for normal transcriptional regulation. In non-erythroid cells, KLF3 distinctly binds to the HS-12 and HS-26 elements and plays a nonredundant, albeit modest, role in the silencing of α-globin expression. [ABSTRACT FROM AUTHOR]
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