FB2026_03 , released September 17, 2026
Clone: Dmel\RE13191
Open Close
General Information
Symbol
Dmel\RE13191
Species
D. melanogaster
Name
RE13191
FlyBase ID
FBcl0194570
Feature type
Computed gene(s)
 
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
      Sequence Data of the Insert
      Full Length Sequence
      Total bases
      1,942
      NCBI
      Full Length sequence dataSequence Downloader
      AGTAATGGCAACGCTGCCCGAAAGACCGAAATTACTTGGTTTTTATTTTGACAACAAATTGGATAAAATGAGTGGCTTGA
      AGGCGAAAAAATCCAGCAAGGGCGACCAAATCCCCAAGCCCATTAGCATTAAGAAGGAGAAGATCGAGGAGGAACGAAAG
      CTGCATCCCATGTCCCATTACATAGACGACCGCCTGGAATTGGTGAAACAGATATTTGGGACCTTAAAACCGAAAACCAT
      TTTGAACCTAGCCCCAGAGTTTCTAAAGAAAACGCCACTAGACGAAATCGAGGAACTTTGTCTGGAGGAGTTACTCTGCT
      TGTCTACGAAGCGGCTAAAATCCATAATAGAAAACACCAAATGTCCCACAGACACTGAAAGCTCCGAAGATTCCGATGTG
      GAGCACAAAGAAGAACACATCTCGCTAGAGGAGATATCATCCGACAGCGACATCGGAGGTCAGGAATCCCGAAAAACCAA
      GAAGAAGCTTAGATCCAAGAAAACGAACAATGGGAATGAAAACAAAGAGTCGGGTGGTCAAATGAGCGTGCTGGAACTGT
      TGGAACTTCAGGCACGTGCCAGGGCCATCCGCTCCCAACTGGCAATGGAGCCAATCACCAAAATAGAGGTCAAGTCAGAT
      GATGATATTGACGAAGTACCAGTGGAGAAAGTACAGCGAAAGGAAAAGGATAAACGCAGCACTAAAAAAACGGATTCGAG
      CAAGCGCAAATCGCAGGAATCAGCTAGACCAACATCTCCATCCCAGCCTGATAGCAGCAGCAAGGAGCAGGAAGCGCCCC
      GCAAAAGAATCAAGATCAAAAGAAACTATAGGCGGACTTCAAAGTCGCCAGAAAAGGAAGTCAAACCTCCAACATCTACT
      ACTTCATCCGAAACTTTGGTTGCATCTAACGATTTAAACAAACTGCCACGTTCCAAATCACGTTCAGCCTCACCAGATGT
      GATACCTATACAAACGGAACCCGAAACACTGCTGATCAGCGACAGTACGGATGATGAGGCCACCAAAAAGAAGACAACTG
      AAACAACTACAACTAAGCAAGTCGAATCGGACCCACCAGCCCCAGTCGTTGAGAGCGAGCCAGAGGAGGGAGAAGTGCGC
      GATGAACCCGAAGAGCCAGCTAAGGTAGTTGACCCAGCCAATCCAGATGAGCCAACAGAGTCAGAAGCAGCAGCTATTTC
      GAAAGAACTGGAAAGTAATAAGCCAGAAGTATCGGATACGTCTGATAAGCTAGATAAAACAGGGGATAAGGAACCACCGT
      CGGAAGAAGCTCTCCCAGCTAATCCCCCTGCAGAGCCAAAGAAGCCGAGTGCAGCCGAGCCAACTGCCCTTGACGACGAA
      GATCAAAACGACGACGTCATTTCAATAGGTGGGGATCTAGAAATGATTGAGGAAATGACGAAGGATGACGATTCACCTTG
      GGTAAGCATTAAAAGCGAGAAAAAGGAGAAGATGCAGGATCCTGAGGAACTGGACAACGATGTCATATCCCTGGACACAA
      GCGAGGATGAACGCGACAAACTACAGCAGGCAGACTCCGAGTCCTGGCGTTCACGCTACATGAAGAGCTCCAAGGTCAGC
      CAGGTGCTGGCCGAATCGCGTTTGGGAAAACGCGTCCGTGACAAGCTCAAGAAATCGAAGCGCACCAAAGTCACCGCCGG
      CGAGGAGCAGGCCAAGGTTGAAAAGCCGGATTCATTTACTTCCAAGCATGAAGACGGATCCATAGAGCAATACCAGGAGC
      TTCTGCAGCACCGACAGCGTAAAACTTCAAACAGTAGCAAGGGGGATAAATAAGTTTAGCCGCTAAGGGCGGGATTTATT
      GAAAAGTCGCGTACTGACGCACGGCCCTAGTTTATATGGCATATAAAAAGTCAAATAAAAATTTGCTGTCCTCGGGGGCG
      GAAGGCCAAAAAAAAAAAAAAA
      
      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)