Neutralizing the function of a β-globin–associated cis-regulatory DNA element using an artificial zinc finger DNA-binding domain

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 109; no. 44; pp. 17948 - 17953
• Main Authors: Barrow, Joeva J, Masannat, Jude, Bungert, Jörg
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 30.10.2012; National Acad Sciences
• Subjects: adults; Animals; Antibodies; beta-Globins - physiology; Binding Sites; Biological Sciences; Cell Line; Cell lines; Chromatin Immunoprecipitation; DNA; DNA - metabolism; DNA-binding proteins; Electrophoretic Mobility Shift Assay; Embryos; Erythroid cells; Gene expression; Genes; Genetic vectors; genetically modified organisms; loci; Mice; Mice, Transgenic; Microscopy, Fluorescence; neutralization; nucleotide sequences; Oligonucleotides; Polymerase Chain Reaction; transcription factors; Zinc; zinc finger motif; Zinc Fingers
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1207677109

Gene expression is primarily regulated by cis -regulatory DNA elements and trans -interacting proteins. Transcription factors bind in a DNA sequence–specific manner and recruit activities that modulate the association and activity of transcription complexes at specific genes. Often, transcription factors belong to families of related proteins that interact with similar DNA sequences. Furthermore, genes are regulated by multiple, sometimes redundant, cis -regulatory elements. Thus, the analysis of the role of a specific DNA regulatory sequence and the interacting proteins in the context of intact cells is challenging. In this study, we designed and functionally characterized an artificial DNA-binding domain that neutralizes the function of a cis -regulatory DNA element associated with adult β-globin gene expression. The zinc finger DNA-binding domain (ZF-DBD), comprising six ZFs, interacted specifically with a CACCC site located 90 bp upstream of the transcription start site (–90 β-ZF-DBD), which is normally occupied by KLF1, a major regulator of adult β-globin gene expression. Stable expression of the –90 β-ZF-DBD in mouse erythroleukemia cells reduced the binding of KLF1 with the β-globin gene, but not with locus control region element HS2, and led to reduced transcription. Transient transgenic embryos expressing the –90 β-ZF-DBD developed normally but revealed reduced expression of the adult β-globin gene. These results demonstrate that artificial DNA-binding proteins lacking effector domains are useful tools for studying and modulating the function of cis -regulatory DNA elements.