General Information
D. melanogaster
Reagent type
FlyBase ID
Created by
A set of transgenic RNAi constructs for expression of shRNA under UAS control, TRiP second generation (pVALIUM22).
    The TRiP-4 construct collection represents a second generation of TRiP lines. Each construct is designed to target the knockdown of a single gene during oogenesis using short hairpin RNA (shRNA).
    NOTE: Dataset members correspond to the amplicon sequence features; these can be used to retrieve associated constructs and stocks.
    Biosample Source
    Tissue isolated
    Other tissues studied
    Cell component
    Cell line
    Key genes
    Sample preparation
    Reagent Details
    Molecular Construct used
    Transgenic Construct used
    Transgenic animals were designed to carry a short hairpin RNA (shRNA) under UAS-GAL4 control. To design the shRNA for any given gene, sequence for all exons, or all exon portions common to all transcripts, were reverse complemented and all possible 21-bp subsequences were determined. Sequences with off-target matches of 16-bp or more were discarded. The remaining sequences were scored as per Vert et al., 2006 (PMID: 17137497). Top and bottom strand oligonucleotides for the top scoring sequence were cloned into pVALIUM22, which by virture of it's P-transposase core promoter, drives excellent knockdown in the germline but little in the soma. The hairpin-containing transgenes were inserted via site-specific recombination into genomic loci known to be optimal for expression, either the P{CaryP}attP2 or P{CaryP}attP40 target element.
    shRNA sequences were predicted for all annotated genes, the vast majority using 'designer of small interfering RNA' (DSIR, Vert et al., 2006, PMID: 17137497). To minimize off­target effects, shRNAs whose guide or passenger strands had complementary matches of 16 nucleotides or more to the fly transcriptome. Only shRNAs that lacked sequence complementarity to annotated microRNA ‘seed’ sequences were considered. A shRNA library representing 83,256 unique synthetic hairpins was synthesized on four custom 22K Agilent microarrays, with up to six shRNAs per gene. Synthetic hairpin constructs were then amplified and cloned into pVALIUM22. Hairpin constructs were based on the backbone of mir-1 with perfect complementarity between the guide and passenger strands, which favors loading onto AGO2 effector complexes. The attB sequence allowed for targeted phiC31-mediated integration at genomic attP landing sites
    Mode of Assay
    Data analysis
    Constructs of the TRiP-3 and TRiP-4 collections deliver a short hairpin RNA that is more effective at knockdown than the long hairpin RNAs used in the first generation TRiP-1 and TRiP-2 construct collections.
    The pVALIUM22-based constructs of the TRiP-4 collection give excellent and specific knockdown in the germline and have little effect in the soma, while the pVALIUM20-based constructs of the TRiP-3 collection give excellent knockdown in the soma and work well in the female germline.
    The second generation of shRNA-based RNAi constructs was developed because first generation, long dsRNA hairpin-based constructs are ineffective in gene knockdown during oogenesis.
    pVALIUM22-based shRNA constructs are not only more effective than pVALIUM20-based shRNA constructs for knockdown in the germline, but they are also strictly restricted to the female germline.
    In compari­son to long­ hairpin constructs, shRNA constructs are expected to be advantageous as they give rise to only two siRNA species, the guide and passenger strands. Nonetheless, off­target effects with shRNAs have been observed, and verification of phenotypes using independent shRNA constructs to the same gene is advised.
    Associated Data
    Associated features
    1,536 RNAi_reagent(s)
    Additional Information
    [TRiP Approach - 2nd generation](
    Synonyms and Secondary IDs (4)
    Reported As
    Symbol Synonym
    shRNAs expressed from Valium22
    Name Synonyms
    A set of transgenic RNAi constructs for expression of shRNA under UAS control, TRiP second generation (pVALIUM22).
    Secondary FlyBase IDs
      References (5)