FB2026_02 , released June 18, 2026
Clone: Dmel\RE58741
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General Information
Symbol
Dmel\RE58741
Species
D. melanogaster
Name
RE58741
FlyBase ID
FBcl0223699
Feature type
Computed gene(s)
 
Collection Status
BDGP
Known Problems
none
FlyBase assessment
  • Caution: This cDNA clone replaced by FI04457
Library
RE_cDNA
  • RE cap-trapped cDNA library of D. melanogaster, iso-1 strain, embryo (0-22 hr).
Strain
    Vector
    Tissue Source
    Stage
    Tissue/Position (including subcellular localization)
    Reference
    Sequence Data of the Insert
    Full Length Sequence
    Total bases
    4,046
    NCBI
    Full Length sequence dataSequence Downloader
    GGAGTGTTTTCTTCGCTCGGATTGATTAAGGGTCCAAAAACATTTTCGAGTAATCTGGGTCGCTTGCTAATTGGAAAACC
    ACTGATCTGAGTTAAGACATAAATGTTTGGACCGCTATTAAATGCAAGGATACGAAAATAGCAAGTAACATGGAAGCCGC
    ATCACCGAGGGAAACCCAGAAGAACCCGAATCCGATCGAGGCGCTGAGCAAAGATGAAATCATCAGCAAATACAAAGGCC
    TGCTCAACATCGCTAAAAAGGCGAAACAGGCAAAAGATGAACTCACCGAGGAAAATCACCGACTCAAGGATGCCCTTAAA
    CGGGCGGCGGAGAAGCAGAGCAGCCTGCCAGCCATGCAGGAAATGGTCCAGGACTTCACCGATAAGAACCTCATCCTCAC
    CGAGGAAGTGAATAATCTGAAACGAAAGACCAAAGAGGATGCCGATCGACTGACGCAATTCGAGATCGAGAACGAGAGCC
    TAAAGCGCCAACTTGGGCGACTGAGTGATGAATACGATGCCCTCCTTGCCAATGTGGATCGCATGGAAAAGGCTATGCAA
    CAGGTCAATGCTCTGGGTAACGAGCAGCGCAAGAATCTGGAACTTTTGGAAGTGGACATTGCCAAAATTAAGGAAGCGGA
    GGCGGAAAACGCTAGTCTTCGCCAGCAAGTCGCCACGATGGAAGAAGAGTCGAGTGTGCTGCAGCAAAAGTACCAAAACA
    TCAAGGAACTTAACTCTGAGCAACGCAAGAAGTTTAATTCTCTAAAGGACCGCTTCATTGATGTACACCGCAAGTTGAAG
    AACCTCAAGGAGTGCAAGTGCGTGCTGCTGGAAACGCAGCACGAGTACGCCGCATCCGTTTCCAAATGGCAGGTGGAGAT
    TATCAAAGCTTCGCAACTGTTGTGCGCAAAGATGGCATCCCTGCAGGCCGAGAATGAAAAACTGAAGCTGAACAATGGAA
    AGTCAGACAATAATCCTCAAACAATTGACACTGGAATTGACCGCAAGCGCTTACTGCAAAGAGTTCAGGAAATGGATCGG
    CTAGCCAAAATAGTGAAGCAGAAGCAAAAGAACCAAAGGAGCAATTTGAATGTGGAGTACCTACTTAAGAAGATAACCGC
    TCTCGAAGAGCTTGCAGTCATTATAAAGCAGCAGCATAGAATTGACAAGGAACAATTGATAAGTGTAACGAAGGAGCAGG
    AAAACACCAAAAATCACGCCAGGAACCTTAATGTAAGCTTATTCCAGACCAAGCTTGATCAAATGCAAAATCTGGTCAAA
    GTCATTGCAAAGGAGCGTGATAATCAGCAGAGGAAGTTGCAGGAGTTGGAAGCCATCTGCATAGAACTGCGCCAACACAA
    CGAGGATTTGCTTACGCGATACCACCTCAAGGAGCAAGAGCATGGAGAGTTGCTAACGGAGATGCGGGAACTGAACGAGG
    CGCTCAAAGGACGCGGTGATGCCATTTCACGCCTTCAAGAACAGCACGAAGCGGAGGTCAAGCGACAACGAGACTTGGAG
    GCTCAACTATCTAATAGTCAGCAGGCGGCGCAGGAGAAGTTACAGAAGATCAAACAACTCCAGAGCCGTGTTGAGGAATT
    GGAGCAGGCGAATGCTGATGCCCAGAGTGATGTTCTGTCGACATCCACAATATCACGAGCCGAAGAACTAAGCCGCCTGC
    GTGAACTGGACGAAGGCTACGAGGAGAAGTACCATAAGCTCAGAGCCATAGCTGCCAAGCTGAAAAAGAAACTGCAGGAG
    CAGACGCAGCAGCTGAATGAAATGGAACAGAGCGGTGCCCTAAAGGAGGAGTTGGAGGCAATCAAGTTGGCACAGGCCCA
    ACTGCAACAGGATTTAAATGCAGCTCGAGCTGAAAACCAGAAGCTAAAGTCCAAGGAGAAAGTAAAGCACTCCAGTGTCC
    TTAATTTGGAAATTGAAGCAGCTGAAAAATCCCTGAGCGAAGTTAGTGCGAAGCTGACAGCTAAGTCTAGCGAACTAGAA
    GCCGTTAAGGAATCACTGGCCAGCAAGGAAAACACCATCGTCCAGCTGCGCAAGGAGATCGCTATCCTAGAGGAGGCCAA
    AAACGGCGAAGCGGCCCACTCCCTAGAACTTAAGGAGCAGATTGATCGCATGCAGGTCCAGGTCAAAGACGCAGTTCACA
    GCAAGCAACAGGCGCTCACTCAGAACAAGGATTTGGAACATGGCGTTGAACAGGCCAAGCTCGAGGCGGAGCAATTGCGT
    CTCCAGCTGTCGGAGAGCGCCCAACAATACGAATCGAAGCTAAACACGGCCACCCAACAACTACTAAGCCAAACCCAGGA
    GCTGGAAATGCACCTGGCAGAGCAAAAGCGATTGGAGACGGCGCTTCGAAATGCGGAACGAGCTCTGGAGGACCTGCGAG
    TAGAGTACACCGAATACAAGTTGAAGGCACAGTCTGTGCTGCGCAAAAACCAAAATAAGGGCTCCAACCGCGAACAGGAG
    TTGGAAGAAGAGTTGGTTGCGCTTCGAGAGAGTGAACGCAATCTGCGCGCCAGCAACGATGGAAGAGCTGCCCGCCTGGC
    CCAGTTGGATAGTCAAATAGAGGAATTGCGACAGGATAACACTGATCTGCAAAAGCGTAGCAAAGAGCTCGTCTCTCTAG
    TTGACGAACTGCGTCAGCAAAACGACCTGCTGTCGCTAGAAAACCAACGCCAGTTGCAATTCCAACACGACCTGATGCAG
    CAGCATCGCCAGCAAGTTGATGAGCTGGACGCCGGGCACCAGTTGCAATTAACGCAGGTGCAGGAGCAACTGGAGGAAGC
    GCAAAAGATGCAAGCAAACGTCTCTCAGCATACCACTGCATCCGCCGCGAGCGTGGACACCAGTCCAGAGCAGGCAAAGA
    TCGATTACTTGCTTATGGACCACGAAACAGGCTTGGATGGCCACGCTGGAGACGTCTCTCTGGCCCAACTGGCTGCTCAG
    CGAAAGATATCTACTGCCTCGAGACGTTCCCACGACTTCATGCCGCTTGACGAGCTGCTCAACACATCAATGAACCAAAT
    AACCAGCGATACCGTGACTACCATCTCTAATTTCGGACGCAGCGTTTCGCAGCAGGAGGACGAGGAAGCGGAAATGGCCG
    CACGGGGAGACTTTTCCGTCCAAAGTGCCCAGCTTCAGGCCACAAAAGAACGCCTAAGCATCCAGGAAAGTCGTGTCAAG
    CACTTGACTGCCCTGTTGGCCGAAAACGAACAGGATTTGGCTAAACTGACCCAAATGAACGACATGCTCAAGGAAGAATT
    GCGCCGCCAAGAGCGCTCCGAGGAACGTGAACAACACATGCACAACTCCGAGTACTTGAAGAACGTCTTCTTAAAGTTCC
    TTACGTTAAACAATGTCGATGAGCGGCAGCGCTTGGTTCCCGTGCTAAATACCATTCTCCGCCTGAGTCGCAACGAAATG
    GAAATGCTGAACTGTGTGGCCAAGGGACAGAAAGTTTCTGCAGATGGTAGCAGTCGCAGCTGGACGGGATTCCTCACTGC
    GTGGAGTGGAGGAGGCAGTCCCAATAATAACAACTAGCGAACATCATAGGATATATAATATATAAATATTCGTCTTGTTG
    GATGCGGATAGTCGTCAGTCGTTGGGCAGTTGCATAGCATTCATTCTGTAAATCTTGTACAATTTCCCTTTTATATATAA
    TGTATTTTAAAATTGCTCGTTGCTGTTTGGCACATCGTACTTTGTACACTCTTGTAATTTGTCCACACCCGTTGTGTTGA
    GTGCCCTATACAGCACCACCGGCAATATGCGCGTTGTAGATTGAAGAAAGCCTTTGCATATATTTAAAAACAATGTTTTT
    CAATGGTTTGTTTAATTTGAAATTCTATTACCATATAGATCAGACTATAAATCAGATGCATTGTCTATAAATTAGTATTC
    CATTATTTGTATTGTATGTACTATATATAAATAGGATCGGTATTTATGCTTACATTTACACTTTTAAACGGTGTATATTG
    TTTACACACAATATAAAATATCATTAACATAAAAAAAAAAAAAAAA
    
    Library Information (1)
    Library: RE_cDNA
    Description

    Cloned cDNAs prepared from polyadenylated RNA isolated from 0-22-hr embryos.

    Sample preparation

    For the RE cDNA library, embryos at 0-22 hr AEL were collected from an isogenic y; cn bw sp (iso-1) strain.

    Protocol

    RNA was polyA+ selected twice (RNA made by L. Hong). cDNA was synthesized by priming with the oligo(dT) primer adapter (5'-GAGAGAGAGAGGATCCAATACTGGAGAGTTTTTTTTTTTTTTTTVN-3'). The first strand was synthesized in presence of trehalose, which increases the full-length cDNA synthesis (Carninci, P. et al. 1998. Proc. Natl. Acad. Sci. U.S.A. 95(2): 520-524; Carninci, P. et al. 1999. Methods Enzymol. 303: 19-44). Full-length cDNA was selected with the biotinylated cap-trapper (Carninci, P. et al. 1996. Genomics 37(3): 327-336). A linker was then ligated to the single-strand cDNA following the published protocol (Shibata, Y., et al. 2001. Biotechniques 30(6): 1250-1254). Subsequently, the cDNA was normalized by using RoT=1.0 as published (Carninci, P., et al. 2000. Genome Res. 10(10): 1617-1630). Second strand cDNA was primed with the (5'-AGAGAGAGAGCTCGAGCTCTAATAAGGTGACACTATAGAACCA-3') primer. After restriction digestion of the hemimethylated cDNA with BamHI and XhoI, the cDNA was cloned in the lambda FLC-I vector. Subsequently, the library was bulk-excised into pFLC-I plasmid as described (Carninci, P., et al. 2001. Genomics 77(1-2): 79-90). cDNAs were transformed into DH5-alpha TonA strain.

    Comment
    Reported As
    Symbol Synonyms
    RE_cDNA
    Riken embryo library
    References (3)
    Research paper (2)
    Hoskins et al., 2011, Genome Res. 21(2): 182--192
    Genome-wide analysis of promoter architecture in Drosophila melanogaster. [FBrf0213090]
    Stapleton et al., 2002, Genome Res. 12(8): 1294--1300
    The Drosophila Gene Collection: identification of putative full-length cDNAs for 70% of D. melanogaster genes. [FBrf0152058]
    Supplementary material (1)
    Hoskins et al., 2011, Genome Res. 21(2):
    Supplemental Material. [FBrf0213251]
    External Crossreferences and Linkouts ( 2 )
    Linkouts
    DGRC - Stock center for Drosophila cDNAs, vectors, and cell lines
    Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
    Synonyms and Secondary IDs (0)
    Reported As
    Symbol Synonym
    Secondary FlyBase IDs
      References (0)