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PMID: 12592412 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Scanning the human genome with combinatorial transcription factor libraries.

Nature biotechnology ·Vol. 21 ·No. 3 ·2003-03-00 ·Pages 269-74

Blancafort P, Magnenat L, Barbas CF

Abstract

Despite the critical importance of transcription factors in mediating gene regulation, there exists no general, genome-wide tool that uses transcription factors to induce or silence a target gene or select for a particular phenotype. In the strategy described here, we prepared large combinatorial libraries of artificial transcription factors comprising three or six zinc-finger domains, and selected transcription factor-DNA interactions able to upregulate several genes in human cells. Selected transcription factors either induced the expression of an endothelial-specific differentiation marker, VE-cadherin, in non-endothelial cell lines or, when combined with a repression domain, knocked down expression. Potential binding sites for a number of these transcription factors were mapped along the promoter of CDH5, the gene encoding VE-cadherin. Transcription factor libraries represent a useful approach for studying and modulating gene function in cells and potentially in whole organisms.

MeSH Terms
Cell Line Combinatorial Chemistry Techniques/methods Gene Expression Profiling/methods Gene Expression Regulation/genetics,physiology Genome, Human Humans Kidney/embryology,metabolism,physiology Peptide Library Proteomics/methods Recombinant Proteins/genetics,metabolism Transcription Factors Transfection/methods Zinc Fingers/genetics
Chemicals
Peptide Library Recombinant Proteins Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Blancafort Pilar
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Magnenat Laurent
Barbas Carlos F
Article Info
Journal
Nature biotechnology
Abbr.
Nat Biotechnol
ISSN
1087-0156
Published
2003-03-00
Epub
2003-00-18
Pages
269-74
Language
English
Region
United States
NLM ID
9604648
Subset
IM
Grants
NCI NIH HHS · CA86258 · United States
NIDDK NIH HHS · DK61803 · United States
Corrections
CommentIn
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