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A recombinase-based palindrome generator capable of producing randomized shRNA libraries.
- Source :
-
Journal of biotechnology [J Biotechnol] 2009 Aug 20; Vol. 143 (2), pp. 79-84. Date of Electronic Publication: 2009 Jun 17. - Publication Year :
- 2009
-
Abstract
- Short hairpin RNA (shRNA)-expressing vectors have been shown stably to knock-down directed targets through RNA interference (RNAi). RNAi has emerged as a powerful tool for reverse genetic screens by assaying cellular phenotypes after exposure to libraries of pooled shRNAs directed against all or a subset of cellular mRNAs. Recently, noncoding RNAs have been recognized as major arbiters of cellular phenotypes. The scope and diversity of noncoding RNAs greatly enlarge the target pool for reversible genetic screens and underscore the desirability as screening tools of complex RNAi libraries, such as randomized RNAi libraries. We describe a novel approach to generate randomized shRNAs that takes advantage of a stable plasmid intermediate that arises in a FLP recombinase system. The ability of this system to generate randomized palindromes represents a new technology for shRNA generation including random shRNAs that cannot be produced synthetically. We describe this plasmid system and its use in generating randomized shRNAs from input 20-bp oligomers, and validate the functionality of a shRNA produced using this approach to knock-down estrogen receptor alpha expression.
- Subjects :
- Cloning, Molecular methods
DNA Nucleotidyltransferases metabolism
Estrogen Receptor alpha genetics
Estrogen Receptor alpha metabolism
Gene Library
RNA, Small Interfering metabolism
Reproducibility of Results
DNA Nucleotidyltransferases genetics
Gene Knockdown Techniques methods
Inverted Repeat Sequences
RNA, Small Interfering genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1873-4863
- Volume :
- 143
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- 19539675
- Full Text :
- https://doi.org/10.1016/j.jbiotec.2009.06.010