Identification of the DNA sequence that interacts with the gut-enriched Kruppel-like factor

被引:163
作者
Shields, JM
Yang, VW
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1093/nar/26.3.796
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 gut-enriched Kruppel-like factor (GKLF) is a recently identified eukaryotic transcription factor that contains three C2H2 zinc fingers. The amino acid sequence of the zinc finger portion of GKLF is closely related to several Kruppel proteins, including the lung Kruppel-like factor (LKLF), the erythroid Kruppel-like factor (EKLF) and the basic transcription clement binding protein 2 (BTEB2). The DNA sequence to which GKLF binds has not been definitively established. In the present study we determined the DNA binding sequence of GKLF using highly purified recombinant GKLF in a target detection assay of an oligonucleotide library consisting of random sequences, Upon repeated rounds of selection and subsequent characterization of the selected sequences by base-specific mutagenesis a DNA with the sequence 5'-(G)/(G)(A)/(A)GG(C)/(T)G(C)/(T)-3' was found to contain the minimal essential binding site for GKLF. This sequence is present in the promoters of two previously characterized genes: the CACCC element of the beta-globin gene, which interacts with EKLF, and the basic transcription element (BTE) of the CYP1A1 gene, which interacts with Sp1 and several Sp1-like transcription factors. Moreover, the selected GKLF binding sequence was capable of mediating transactivation of a linked reporter gene by GKLF in co-transfection experiments. Our results establish GKLF as a sequence-specific transcription factor likely involved in regulation of expression of endogenous genes.
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页码:796 / 802
页数:7
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