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1.
Genome Res ; 13(10): 2325-32, 2003 Oct.
Article in English | MEDLINE | ID: mdl-12975310

ABSTRACT

RNA interference is a powerful tool for studying gene function and for drug target discovery in diverse organisms and cell types. In mammalian systems, small interfering RNAs (siRNAs), or DNA plasmids expressing these siRNAs, have been used to down-modulate gene expression. However, inefficient transfection protocols, in particular, for primary cell types, have hampered the use of these tools in disease-relevant cellular assays. To be able to use this technology for genome-wide function screening, a more robust transduction protocol, resulting in a longer duration of the knock-down effect, is required. Here, we describe the validation of adenoviral vectors that express hairpin RNAs that are further processed to siRNAs. Infection of cell lines, or primary human cells, with these viruses leads to an efficient, sequence-specific, and prolonged reduction of the corresponding target mRNA, resulting in a reduction of the encoded protein level in the cell. For knock-down of one of the targets, GalphaS, we have measured inhibition of ligand-dependent, G-protein-coupled signaling. It is expected that this technology will prove to be of great value in target validation and target discovery efforts.


Subject(s)
Adenoviridae/genetics , Genes/physiology , Genetic Vectors/biosynthesis , Genetic Vectors/physiology , RNA, Small Interfering/biosynthesis , RNA, Small Interfering/physiology , Adult , Arthritis, Rheumatoid/pathology , Cell Line , DNA, Viral/genetics , Endothelium, Vascular/chemistry , Endothelium, Vascular/cytology , Endothelium, Vascular/virology , Epidermal Cells , Fibroblasts/cytology , Fibroblasts/pathology , Fibroblasts/virology , Gene Expression Regulation/genetics , Genetic Vectors/chemistry , Genome, Human , Humans , Keratinocytes/chemistry , Keratinocytes/virology , Nucleic Acid Conformation , RNA, Small Interfering/chemistry , Structure-Activity Relationship , Synovial Membrane/pathology , Transfection , Umbilical Veins
2.
Nat Biotechnol ; 20(11): 1154-7, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12355097

ABSTRACT

With the publication of the sequence of the human genome, we are challenged to identify the functions of an estimated 70,000 human genes and the much larger number of proteins encoded by these genes. Of particular interest is the identification of gene products that play a role in human disease pathways, as these proteins include potential new targets that may lead to improved therapeutic strategies. This requires the direct measurement of gene function on a genomic scale in cell-based, functional assays. We have constructed and validated an individually arrayed, replication-defective adenoviral library harboring human cDNAs, termed PhenoSelect library. The adenoviral vector guarantees efficient transduction of diverse cell types, including primary cells. The arrayed format allows screening of this library in a variety of cellular assays in search for gene(s) that, by overexpression, induce a particular disease-related phenotype. The great majority of phenotypic assays, including morphological assays, can be screened with arrayed libraries. In contrast, pooled-library approaches often rely on phenotype-based isolation or selection of single cells by employing a flow cytometer or screening for cell survival. An arrayed placental PhenoSelect library was screened in cellular assays aimed at identifying regulators of osteogenesis, metastasis, and angiogenesis. This resulted in the identification of known regulators, as well as novel sequences that encode proteins hitherto not known to play a role in these pathways. These results establish the value of the PhenoSelect platform, in combination with cellular screens, for gene function discovery.


Subject(s)
Adenoviridae/genetics , Gene Expression Regulation, Viral , Gene Library , Genome, Human , Animals , Cell Line , Dogs , Epithelium/physiology , Epithelium/virology , Feasibility Studies , Female , HeLa Cells/physiology , HeLa Cells/virology , Humans , Kidney/physiology , Kidney/virology , Neovascularization, Physiologic/genetics , Oligonucleotide Array Sequence Analysis/methods , Osteoblasts/physiology , Osteoblasts/virology , Placenta/physiology , Placenta/virology , Pregnancy , Sequence Analysis, DNA/methods
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