FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Clone: Dmel\RE08932
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General Information
Symbol
Dmel\RE08932
Species
D. melanogaster
Name
RE08932
FlyBase ID
FBcl0200316
Feature type
cDNA_clone
Computed gene(s)
Dmel\CG31259
 
Collection Status
DGC gold BDGP
Known Problems
none
FlyBase assessment
    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
      embryonic stage
      organism

      Comment: 0-22 hr AEL

      (Stapleton et al., 2002)
      Sequence Data of the Insert
      Full Length Sequence
      Total bases
      1,933
      NCBI
      AY071002
      Full Length sequence dataSequence Downloader
      TGGGACCGTACTTGGCCAAATCGGCAGTCAGTTGTATTTGATGGCCGACCAGGCCATAACGTGGTTTCCTAGTAGGAGAA
AATATTATTAAATAACCAACGTGCCATAACAACTAAATAAACAACCAATGCTAGTTCCTTGCTGAAGCTTGTCGTATTTT
TTAGTTGACATATATGCAGCTGAGACCAAGTGGATAACAAGCTGCAGCTGATTCGAGGAATGCCCAGCGTCATTTACTGC
GAATCGAGCAATTTGGATCATCGAATTTTTAACTGCATTCATTAGATTTTCAAGCTGAAATTACACTGGATTAATCGTAA
GTCCGGGAAATCGAGTTGAACTAGGCCATTGTGGACATTGCGTGCCACGTTCGAACTTTTGGCGATAAGCCCCTTCTCGA
TAAGCTTTATCATCCCCACGAAGCCAATTCGTTAATCGTCGACGGCGGAGCATAAGTCAATATTCAAAGTGGATCATGGG
CGCCCAAAGTAAACTGGCCGAGATAGCCTTGAACTGCACCTGCTATGAGTATCACCATCCGTGGACAAAGAGCTGTGCCT
GCGCTGCGGCAGGAATGATGATCTCTGAGATCCCTCCCAGTCTGCGCACCTACGCCACTGTATACGTGTTTGCTCTAATC
ATGCGAGGACGCATTCCATCGCTGAAGGATCTGAGACGCACTGCATCTGGAATCCTACAGTCGACAGCGTTTCTTTCGAT
GAATGGAGGCCTCTTTGTCTTTGCCGTGTGCTACTTGCGACAGATCTTGGGAGGATTCTACTTCGGCACAGTTGCTTGGC
TGCCCTCGTTTTTGGCCAGCTTTGCATGTCTTGCCTTCGAGCGTCCGGAACGCCGTGCTCCTCTCGCATTGTATGTGGCC
AATGTGGGTATCGAAACGCTGTGGAAGATGATGGAGGCACGAGGCTGGGTTCGATCCATTCCTAATGGACAGGTGTTCAT
CATGGGTGCAAGTGTGACCGCCTTGATGTATTTATATCGCGCCGGATTGCACAAGACAGTGGCCAAGGATCCGACGTTCA
AGGCTATTGCCCTGATCGTGGGCAAAGAGGACGAGGGTCCACTGAAGACACCGGTGGTCACCACCACGCAAAGCTCTCGC
CAGGCTCCCCTCAACTTCCAAAGCATTTCAGCCTACGTACAGCTCTATGACCGCATGCTGAAGGCCAAACATCCAAGTTG
TCCCCACAAGAGGGGCTGTGTTCCCTACGCCCTTATTGGAGGACTAAAGCCATTCCTGGGCGGTGTTGGCCTATCGGTGG
GTCTAAAGCTGCTGCTCAACATTCCCAAGATCTTTAAGTCTAAGATGCAGTGGCGCAAGCACATCTTCAACGGGGGATCC
TTGCAGTTGGGATTGGCGCTGGGCATCTTCTCATTTCTTTTCAAGTCGACTACCTGCGGACTGCGTCACACGTTTGGTTT
CGACAATGCTCTCTTCGCCATTCCGGCTGGCCTCATCGGATCGATTGGCTTCTTCCGTTTCCCGAACACCACGGTGGCCT
GTTATCTAATGTGGAAGTCCATGCATCTGCTCTACAACTGGGGCATCGCGGAGGGCAAGTTGCCCGAGGTGCCGCACTTT
GCGATGCTCATGTACGGATTCTTCACGGCCGTGCTCTTCCACTCGGCAATCCTGGAGGCTCGTTCCCTGCGGCCCAGCTA
CTACAAGTTCCTCATGGGCATCTCCGGAAATCGCATCAGTCGCTTTAATGTGAAGCCCTTCGAGGCTTACGGACTGAAGA
GCCAGGACCAGATCAACTATGTGATCAAGAAACTGGGCATCGACATGACCTCACCCTTCCCCCTTTACGCCCTGACTGTC
TAGATGGGTTTCCCCCATAACTTCGCATACCTACTGTACAGTAAAAAAAAAAAACAGAAACAATAAATGTGTAACACAAA
AAAAAAAAAAAAA
      Library Information (1)
      Library: RE_cDNA
      Description

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

      (Stapleton et al., 2002)
      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.

      (Stapleton et al., 2002)
      Comment
      Reported As
      Symbol Synonyms
      RE
      (Stapleton et al., 2002)
      RE EST
      (Stapleton et al., 2002)
      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)