Cloning the cDNA for a New Human Zinc Finger Protein Defines a Group of Closely Related Krüppel-like Transcription Factors
We have identified a novel zinc finger protein that has been named ubiquitous Krüppel-like factor (UKLF) based on structural considerations and the pattern of gene expression. UKLF was isolated by the polymerase chain reaction approach using degenerate oligonucleotides corresponding to the DNA-bind...
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Published in | The Journal of biological chemistry Vol. 273; no. 43; p. 28229 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
American Society for Biochemistry and Molecular Biology
23.10.1998
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Online Access | Get full text |
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Summary: | We have identified a novel zinc finger protein that has been named ubiquitous Krüppel-like factor (UKLF) based on structural
considerations and the pattern of gene expression. UKLF was isolated by the polymerase chain reaction approach using degenerate
oligonucleotides corresponding to the DNA-binding domain of erythroid Krüppel-like factor (EKLF) and cDNA prepared from human
vascular endothelial cells. The carboxyl-terminal portion of UKLF contains three zinc fingers of the Cys 2 -His 2 type and binds in vitro to the CACCC motif of the β-globin promoter and to the Sp1 recognition sequence. The amino-terminal portion of UKLF consists
of a hydrophobic region rich in serines and a negatively charged segment with several glutamic acid residues. The first 47
amino acids of the acidic region are nearly identical to the amino-terminal portion of another Krüppel-like factor, the so-called
core promoter-binding protein (CPBP) or Zf9. Like CPBP/Zf9, UKLF can function as a transcription activator in co-transfection
assays. However, this activity is lost when the highly conserved amino-terminal segment is deleted. These findings indicate
that UKLF and CPBP/Zf9 represent a distinct subgroup of closely related Krüppel-like activators of transcription. Mapping
of the UKLF gene to chromosome 2 suggested that UKLF and CPBP/Zf9 translocated to different chromosomes following duplication
from an ancestral gene. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.273.43.28229 |