Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9137582 | Blood Cells, Molecules, and Diseases | 2005 | 9 Pages |
Abstract
Krüppel-like factors (KLFs) have been systematically screened as potential candidates to regulate human γ-globin gene expression through its CACCC element. Initially, 21 human proteins that have close sequence similarity to EKLF/KLF1, a known regulator of the human β-globin gene, were identified. The phylogenetic relationship of these 22 KLF/Sp1 proteins was determined. KLF2/LKLF, KLF3/BKLF, KLF4/GKLF, KLF5/IKLF, KLF8/BKLF3, KLF11/FKLF, KLF12/AP-2rep and KLF13/FKLF2 were chosen for functional screening. Semi-quantitative RT-PCR demonstrated that all eight of these candidates are present in human erythroid cell lines, and that the expression of the KLF2, 4, 5 and 12 mRNAs changed significantly upon erythroid differentiation. Each of the eight KLF mRNAs is expressed in mouse erythroid tissues, throughout development. UV cross-linking assays suggest that multiple erythroid proteins from human cell lines and chicken primary cells interact with the γ-globin CACCC element. In co-transfection assays in K562 cells, it was demonstrated that KLF2, 5 and 13 positively regulate, and KLF8 negatively regulates, the γ-globin gene through the CACCC promoter element. The data collectively suggest that multiple KLFs may participate in the regulation of γ-globin gene expression and that KLF2, 5, 8 and 13 are prime candidates for further study.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Molecular Biology
Authors
Ping Zhang, Priyadarshi Basu, Latasha C. Redmond, Pamela E. Morris, Jeremy W. Rupon, Gordon D. Ginder, Joyce A. Lloyd,