Erythroid Kruppel-like factor directly activates the basic Kruppel-like factor gene in erythroid cells

被引:73
|
作者
Funnell, Alister P. W.
Maloney, Christopher A.
Thompson, Lucinda J.
Keys, Janelle
Tallack, Michael
Perkins, Andrew C.
Crossley, Merlin
机构
[1] Univ Sydney, Merlin Crossley Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4067, Australia
关键词
D O I
10.1128/MCB.01658-06
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Sp/Kriippel-like factor (Sp/KIf) family is comprised of around 25 zinc finger transcription factors that recognize CACCC boxes and GC-rich elements. We have investigated basic Kruppel-like factor (Bklf/Klf3) and show that in erythroid tissues its expression is highly dependent on another family member, erythroid Kruppel-like factor (Eklf/Kif1). We observe that Bklf mRNA is significantly reduced in erythroid tissues from Eklf-null murine embryos. We find that Bklf is driven primarily by two promoters, a ubiquitously active GC-rich upstream promoter, la, and an erythroid downstream promoter, 1b. Transcripts from the two promoters encode identical proteins. Interestingly, both the ubiquitous and the erythroid promoter are dependent on Eklf in erythroid cells. Eklf also activates both promoters in transient assays. Experiments utilizing an inducible form of Eklf demonstrate activation of the endogenous Bklf gene in the presence of an inhibitor of protein synthesis. The kinetics of activation are also consistent with Bklf being a direct Eklf target. Chromatin immunoprecipitation assays confirm that Eklf associates with both Bklf promoters. Eklf is typically an activator of transcription, whereas Bklf is noted as a repressor. Our results support the hypothesis that feedback cross-regulation occurs within the Sp/Klf family in vivo.
引用
收藏
页码:2777 / 2790
页数:14
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