Generation of transgenic drosophila expressing shRNAs in the miR-1 backbone

Chang, K., Marran, K., Valentine, A., Hannon, G. J. (2014) Generation of transgenic drosophila expressing shRNAs in the miR-1 backbone. Cold Spring Harbor Protocols, 2014 (5). pp. 501-509. ISSN 19403402

URL: https://www.scopus.com/inward/record.uri?eid=2-s2....
DOI: 10.1101/pdb.prot080762

Abstract

In Drosophila, long-term effects of RNA interference (RNAi) must be achieved by integrating into the genomea template fromwhich anRNAi trigger is transcribed by cellularRNApolymerases, generallyRNA polymerase II or III. With encoded triggers, not only can essentially permanent silencing be achieved, but control can also be exerted over the level of trigger expression, with a resulting variation in the degree to which the target is silenced. Knockdown can also be controlled in a temporal and cell-type-dependent fashionthroughtheuseofwell-establishedtransgenicmethodologiesandwell-testedpromoters.The forms of encoded triggers vary. Long double-stranded RNAs can be expressed as extended inverted repeats. The nearest equivalent of a small interfering RNA is an artificial microRNA (miRNA) or short hairpin RNA (shRNA),whereanaturalmiRNAbackbone(alsocalledascaffold) isremodeledtoproduceadifferent small RNA or a small inverted repeat (<30 nucleotides) is simply expressed. This protocol describes creation of transgenic Drosophila carrying shRNAinserts in a remodeled endogenousmiRNAbackbone.The protocol applies to the use of miRNA-based shRNAs, butmost of the vectors, principles of experimental design, and methods are also applicable to long inverted repeat transgenes.

Item Type: Paper
Subjects: bioinformatics > genomics and proteomics > genetics & nucleic acid processing > protein structure, function, modification > protein types > enzymes > RNA polymerase
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > genes, structure and function > gene expression
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > oligonucleotide
CSHL Authors:
Communities: CSHL labs > Chang lab
CSHL labs > Hannon lab
Depositing User: Adrian Gomez
Date: 2014
Date Deposited: 22 Nov 2019 20:03
Last Modified: 15 Nov 2023 17:07
PMCID: PMC4377507
Related URLs:
URI: https://repository.cshl.edu/id/eprint/38723

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