FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Clone: Dmel\RE73180
Open Close
General Information
Symbol
Dmel\RE73180
Species
D. melanogaster
Name
RE73180
FlyBase ID
FBcl0230143
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
      2,169
      NCBI
      Full Length sequence dataSequence Downloader
      AGTGTCGATCGATAGTGTCAACTCTAGTCGGCCCACAGCGACGACGCCGCGTAAAATATTTTTGTTTCTCCGCATTCGTT
      GAAAAACAGCGACAATTGCTTGTTTTTATGTGTGGTGCGCGTCCCAGGCAAATGCAAACGAGTCCGCGACTTCAATTGCC
      GAACGCCTAACGCCACCGTGAATAGAAAATAATAGTGATGCGAAAGACCCGCTCTCAGACGGCTCGCACGCAGGCGGAAA
      ATGCCGCAACATCTTCGAGCCCCGGGCACCAGTCGACTTCGTCAGCGCCAATAGCAGTTAATCCCTTTGATTCCACCAAG
      TACAAGGAATGTGAGCAAATGGTGCAGATGCTTCGAGTGGTCGAGCTGCAAAAAATCCTGTCGTTTCTGAACATCTCATT
      CGCTGGACGAAAAACTGACCTGCAGAGCCGCATCCTCTCGTTCTTGCGCACCAACTTGGAACTGCTTGCCCCGAAGGTCC
      AGGAAGTCTACGCCCAGTCCGTGCAGGAACAAAACGCCACGCTGCAGTACATCGACCCAACCAGGATGTACTCGCACATC
      CAGCTGCCGCCCACCGTGCAGCCCAATCCCGTGGGCCTCGTGGGCAGCGGCCAAGGTGTGCAAGTGCCCGGCGGCCAGAT
      GAATGTGGTCGGCGGCGCACCCTTCCTCCACACACACAGCATCAACAGCCAGCTGCCTATTCACCCCGATGTGCGGCTGA
      AAAAGCTAGCCTTCTACGATGTACTCGGAACGCTAATTAAGCCTTCAACTCTGGTGCCACGCAACACTCAGCGCGTCCAA
      GAGGTGCCTTTCTACTTCACGCTCACGCCGCAGCAGGCCACCGAGATTGCCTCTAATCGCGACATTCGCAACAGCTCCAA
      GGTGGAGCACGCCATTCAGGTTCAACTGCGCTTTTGCCTGGTGGAGACTTCGTGCGACCAGGAGGACTGCTTCCCGCCGA
      ACGTAAACGTCAAAGTGAACAACAAACTCTGTCAGCTGCCTAATGTCATTCCTACAAACCGACCAAATGTGGAGCCCAAG
      CGTCCGCCGCGACCCGTTAATGTCACGTCCAATGTAAAGCTGTCGCCTACCGTCACCAACACCATAACGGTTCAGTGGTG
      TCCGGACTACACTCGTAGCTACTGTCTGGCCGTATACCTGGTAAAGAAGCTCACCTCAACACAGCTTTTGCAGCGAATGA
      AGACGAAGGGCGTAAAACCAGCGGACTACACGCGAGGCTTAATCAAAGAGAAGCTGACTGAGGATGCTGACTGCGAAATA
      GCCACCACTATGCTGAAGGTTTCCCTTAACTGCCCGTTGGGCAAGATGAAAATGTTGCTGCCTTGTCGAGCATCAACCTG
      CTCGCATCTGCAATGCTTCGATGCCAGTCTCTACCTGCAAATGAATGAGCGTAAGCCCACGTGGAACTGCCCTGTATGCG
      ACAAGCCGGCCATTTATGACAACCTGGTCATAGATGGCTACTTCCAGGAGGTGTTGGGCTCGTCGCTTCTAAAGAGTGAT
      GATACTGAGATTCAACTTCATCAGGATGGATCTTGGAGCACACCAGGACTACGGAGCGAGACGCAGATCCTTGATACGCC
      TTCAAAGCCCGCCCAAAAGGTTGAGGTTATATCGGATGACATAGAACTTATCTCGGATGACGCCAAGCCAGTAAAGAGGG
      ATTTGTCCCCAGCACAGGACGAACAGCCCACATCAACGTCAAACAGTGAAACTGTTGACCTAACGTTAAGCGATTCAGAC
      GACGACATGCCGCTGGCTAAGCGTCGTCCGCCCGCCAAGCAAGCCGTCGCCAGTTCCACGTCGAACGGCAGCGGTGGCGG
      CCAACGTGCCTATACCCCGGCACAGCAGCCCCAGCAATCCGGTGGTAATGTTTTTAAAAAACCTCAGAAAGCGGAGGAGC
      TTTACAAGCGTGTTCATTTAGGAGTTTGGCTGCGCCCACGAAAACCCAAGCCAGAGAGCTCAAGGCGCCCAAACGTCGGC
      TAAGCAAAGTTAATAGAGTATTTTTCGGTTTTATACCACCATTTGTCCTAATTCATTTTCAATGTATTTTCTGTTGTCAC
      CGAATCTAAATTATTTCACGATATGTACTCTTATTTTAAGTGATAATTTTAATAAATCATGCCAGTTTGTTAGAAAAAAA
      AAAAAAAAA
      
      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 ( 1 )
      Linkouts
      DGRC - Stock center for Drosophila cDNAs, vectors, and cell lines
      Synonyms and Secondary IDs (0)
      Reported As
      Symbol Synonym
      Secondary FlyBase IDs
        References (0)