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本文引用的文献

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KLF8 transcription factor participates in oncogenic transformation.KLF8转录因子参与致癌转化。
Oncogene. 2007 Jan 18;26(3):456-61. doi: 10.1038/sj.onc.1209796. Epub 2006 Jul 10.
2
Alterations in expression and chromatin configuration of the alpha hemoglobin-stabilizing protein gene in erythroid Kruppel-like factor-deficient mice.红系 Kruppel 样因子缺陷小鼠中α血红蛋白稳定蛋白基因的表达及染色质构型改变
Mol Cell Biol. 2006 Jun;26(11):4368-77. doi: 10.1128/MCB.02216-05.
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Genome-wide analysis of mammalian promoter architecture and evolution.哺乳动物启动子结构与进化的全基因组分析。
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Sumoylation delimits KLF8 transcriptional activity associated with the cell cycle regulation.SUMO化作用限制了与细胞周期调控相关的KLF8转录活性。
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Human KLF17 is a new member of the Sp/KLF family of transcription factors.人类KLF17是转录因子Sp/KLF家族的新成员。
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A global role for EKLF in definitive and primitive erythropoiesis.EKLF在确定性和原始红细胞生成中的全局作用。
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Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.转录调控的多样化:人类基因假定替代启动子的大规模鉴定与表征
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High frequency of alternative first exons in erythroid genes suggests a critical role in regulating gene function.红细胞基因中高频出现的可变首个外显子表明其在调节基因功能方面发挥关键作用。
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Antisense transcription in the mammalian transcriptome.哺乳动物转录组中的反义转录
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红系Krüppel样因子直接激活红系细胞中的碱性Krüppel样因子基因。

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

作者信息

Funnell Alister P W, Maloney Christopher A, Thompson Lucinda J, Keys Janelle, Tallack Michael, Perkins Andrew C, Crossley Merlin

机构信息

School of Molecular and Microbial Biosciences, G08, University of Sydney, Sydney, NSW 2006, Australia.

出版信息

Mol Cell Biol. 2007 Apr;27(7):2777-90. doi: 10.1128/MCB.01658-06. Epub 2007 Feb 5.

DOI:10.1128/MCB.01658-06
PMID:17283065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1899893/
Abstract

The Sp/Krüppel-like factor (Sp/Klf) family is comprised of around 25 zinc finger transcription factors that recognize CACCC boxes and GC-rich elements. We have investigated basic Krüppel-like factor (Bklf/Klf3) and show that in erythroid tissues its expression is highly dependent on another family member, erythroid Krüppel-like factor (Eklf/Klf1). 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, 1a, 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.

摘要

Sp/Krüppel样因子(Sp/Klf)家族由大约25种锌指转录因子组成,这些因子可识别CACCC盒和富含GC的元件。我们研究了基础Krüppel样因子(Bklf/Klf3),发现其在红系组织中的表达高度依赖于另一个家族成员——红系Krüppel样因子(Eklf/Klf1)。我们观察到,在Eklf基因敲除小鼠胚胎的红系组织中,Bklf mRNA显著减少。我们发现Bklf主要由两个启动子驱动,一个是普遍活跃的富含GC的上游启动子1a,另一个是红系下游启动子1b。来自这两个启动子的转录本编码相同的蛋白质。有趣的是,在红系细胞中,普遍存在的启动子和红系启动子都依赖于Eklf。在瞬时分析中,Eklf也能激活这两个启动子。利用可诱导形式的Eklf进行的实验表明,在存在蛋白质合成抑制剂的情况下,内源性Bklf基因被激活。激活的动力学也与Bklf是Eklf的直接靶点一致。染色质免疫沉淀分析证实Eklf与Bklf的两个启动子都有关联。Eklf通常是转录激活因子,而Bklf则被认为是转录抑制因子。我们的结果支持了Sp/Klf家族在体内发生反馈交叉调节的假说。