FB2026_02 , released June 18, 2026
Reference Report
Open Close
Reference
Citation
Zheng, X. (2019.3.1). Constructs and insertions from Xiangzhong Zheng. 
FlyBase ID
FBrf0241761
Publication Type
Personal communication to FlyBase
Abstract
PubMed ID
PubMed Central ID
Text of Personal Communication
The following information accompanied stocks donated to the Bloomington Drosophila Stock Center by Xiangzhong Zheng, Indiana University.
P{UAS-foxo.DeltaC.V5} The coding sequence of foxo lacking the C-terminal activation domain was fused in frame with V5 tag and inserted into the pP{UAST} vector. It expresses a dominant negative FOXO that binds to target DNA sequences but incapable of transcriptional activation of target genes under the control of UAS sequences.
P{UAS-foxo.dsRNA} An inverted repeat of foxo coding sequences (~500 bp) was inserted into the transformation vector pP{UAST}. It expresses a dsRNA against foxo under the control of UAS sequences.
P{foxo-GAL4} A 5000 bp promoter fragment of foxo was inserted into the transformation vector pP{PTGAL}. It expresses GAL4 under the control of foxo promoter sequences.
P{hs-HA.smt3} The coding sequence of smt3 with a HA tag at the N-terminus was inserted into the transformation vector pP{CaSpeR-hs}. It expresses HA-tagged SMT3 under the control of the hsp70 promoter sequence.
P{hs-smt3.HA} The coding sequence of smt3 with a HA tag at the C-terminus was inserted into the transformation vector pP{CaSpeR-hs}. It expresses HA-tagged SMT3 under the control of the hsp70 promoter sequence.
P{Cam.CGCGbox-luc2P} An enhancer (~ 125 bp) containing multimeric CGCG Box sequences (A/C/G)CGCG(G/T/C) of the Cam gene and the hsp70 basal promoter was placed upstream of the luciferase reporter gene luc2P and subcloned into the pP{CaSpeR-4} vector. It expresses a destabilized luciferase luc2P under the control of Cam CGCG Box sequences.
P{hs-Rheb} The coding sequence of Rheb was inserted into the transformation vector pP{CaSpeR-hs}. It expresses RHEB under the control of the hsp70 promoter sequence.
P{hs-Pten} The coding sequence of Pten was inserted into the transformation vector pP{CaSpeR-hs}. It expresses PTEN under the control of the hsp70 promoter sequence.
P{hs-AMPKalpha} The coding sequence of AMPKalpha was inserted into the transformation vector pP{CaSpeR-hs}. It expresses AMPKalpha under the control of the hsp70 promoter sequence.
P{UAS-gig.wiz} A fragment of the gig coding sequences (~500 bp) was inserted into the transformation vector pWIZ. It expresses a dsRNA against gig under the control of UAS sequences.
P{UAS-gig.DeltaGAP} The coding sequence of gig lacking the GAP domain was inserted into the transformation vector pP{UAST}. It expresses a dominant negative TSC2 capable of binding to TSC1 but lacks the GAP activity towards RHEB.
P{UAS-Pkc53E.RB} The coding sequence of Pkc53E RB isoform was inserted into the transformation vector pP{UAST}. It expresses PKC53E under the control of UAS sequences.
P{mir-275.mir-305} A genomic DNA fragment (~ 4 kb) containing mir-275 and mir-305 was inserted into the pP{CaSpeR-4} vector. It expresses mir-275 and mir-305 under the control of their own promoter sequence.
P{mir-275-GAL4} A genomic DNA fragment (~ 3.4 kb) containing the mir-275 promoter sequence was inserted into the transformation vector pP{PTGAL}. It expresses GAL4 under the control of mir-275 promoter sequence.
P{per.S820A.S822A} This construct was generated using a similar approach described in Garbe et al. (2013), PLoS Genet. 9(9): e1003749(FBrf0222889). The per promoter and coding sequence with the Ser820 and Ser822 codons mutated to Ala was inserted into the transformation vector pP{CaSpeR-4}. It expresses PER.S820A.S822A under the control of per promoter sequence.
P{per.S809A} This construct was generated using a similar approach described in Garbe et al. (2013), PLoS Genet. 9(9): e1003749(FBrf0222889). The per promoter and coding sequence with the Ser809 codon mutated to Ala was inserted into the transformation vector pP{CaSpeR-4}. It expresses PER.S809A under the control of per promoter sequence.
P{per.S820A} This construct was generated using a similar approach described in Garbe et al. (2013), PLoS Genet. 9(9): e1003749(FBrf0222889). The per promoter and coding sequence with the Ser820 codon mutated to Ala was inserted into the transformation vector pP{CaSpeR-4}. It expresses PER.S820A under the control of per promoter sequence.
P{UAS-Txl.C33S} The coding sequence with the Cys33 codon mutated to Ser was inserted into the transformation vector pP{UAST}. It expresses TXL.C33S under the control of UAS sequences.
P{UAS-Txl.C36S} The coding sequence with the Cys36 codon mutated to Ser was inserted into the transformation vector pP{UAST}. It expresses TXL.C36S under the control of UAS sequences.
P{UAS-Txl.V5} The coding sequence of Txl with the V5 tag in frame at the C-terminus was inserted into the transformation vector pP{UAST}. It expresses V5-tagged TXL under the control of UAS sequences.
P{UAS-Txl} The coding sequence of Txl was inserted into the transformation vector pP{UAST}. It expresses TXL under the control of UAS sequences.
P{UAS-MagR.DM} The coding sequence of MagR from Drosophila melanogaster was inserted into the transformation vector pP{UAST}. It expresses MagR.DM under the control of UAS sequences.
P{UAS-MagR.DP} The coding sequence of MagR from the monarch butterfly (Danaus plexippus) was inserted into the transformation vector pP{UAST}. It expresses MagR.DP under the control of UAS sequences.
P{UAS-foxo.DeltaC.V5}1 is an X chromosome insertion, homozygous viable and fertile.
P{UAS-foxo.DeltaC.V5}3 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-foxo.dsRNA}3 is a third chromosome insertion, homozygous viable and fertile.
P{foxo-GAL4}9A1 is an X chromosome insertion, homozygous viable and fertile.
P{hs-HA.smt3}2 is a second chromosome insertion, homozygous viable and fertile.
P{hs-HA.smt3}3 is a third chromosome insertion, homozygous viable and fertile.
P{hs-smt3.HA}2 is a second chromosome insertion, homozygous viable and fertile.
P{hs-HA.smt3}1 is an X chromosome insertion, homozygous viable and fertile.
P{Cam.CGCGbox-luc2P}2 is a second chromosome insertion, homozygous viable and fertile.
P{hs-Rheb}9 is a second chromosome insertion, homozygous viable and fertile.
P{hs-Pten}3C1 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-gig.wiz}2C1 is a second chromosome insertion, homozygous viable and fertile.
P{UAS-gig.wiz}3A1 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-gig.DeltaGAP}1-10 is a second chromosome insertion, homozygous viable and fertile.
P{hs-AMPKalpha}2 is a second chromosome insertion, homozygous viable and fertile.
P{hs-AMPKalpha}3 is a third chromosome insertion.
P{UAS-Pkc53E.RB}3 is a third chromosome insertion.
P{mir-275.mir-305}1 is an X chromosome insertion, homozygous viable and fertile.
P{per.S820A.S822A}3 is a third chromosome insertion, homozygous viable and fertile.
P{per.S809A}2 is a second chromosome insertion, homozygous viable and fertile.
P{per.S820A}2A1 is a second chromosome insertion, homozygous viable and fertile.
P{mir-275-GAL4}3 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-Txl.C33S}6 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-Txl.C36S}2 is a third chromosome insertion.
P{UAS-Txl.C36S}1 is a second chromosome insertion, homozygous viable and fertile.
P{UAS-Txl.C33S}2 is a second chromosome insertion.
P{UAS-Txl.V5}1B1 is an X chromosome insertion, homozygous viable and fertile.
P{UAS-Txl.V5}3B1 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-Txl}3A1 is a third chromosome insertion, homozygous viable and fertile.
P{UAS-Txl}2A1 is a second chromosome insertion, homozygous viable and fertile.
P{UAS-MagR.DM}5 is a third chromosome insertion.
P{UAS-MagR.DP}2 is a second chromosome insertion.
P{UAS-MagR.DP}6 is a third chromosome insertion.
TxlDelta255 The coding sequence of Txl was deleted through imprecise excision of P{EPgy2}CG10576EY07625. It is a null allele.
CG12795Delta118 The coding sequence of CG12795 was deleted through imprecise excision of P{EPgy2}CG12795EY03155. It is a null allele. CG12795 is a homolog of aip-1 in C.elegans.
Pkc53EDelta28 The coding sequence of Pkc53E was deleted through imprecise excision of P{EPgy2}Pkc53EEY14093. It is a null allele.
DOI
Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Abbreviation
    Title
    ISBN/ISSN
    Data From Reference
    Alleles (27)
    Genes (18)
    Natural transposons (1)
    Insertions (36)
    Experimental Tools (6)
    Transgenic Constructs (23)