GCTTTTCTTTCCTAGCCACGACGAGGTCGACAGCATGAGTTCTCTAAAGCTCCAGAAGAGGCTCGCAGCCTCCGTGCTGC GATGCGGCAAGAAGAAGGTCTGGTTGGATCCCAATGAAATCAACGAGATCGCTAACACAAACTCGCGTCAGAACATTCGC AAGCTTATCAAGGATGGTCTGATCATCAAGAAGCCCGTCGTGGTCCACTCCCGTTACCGTGTGCGCAAAAACACCGAGGC CCGCCGCAAGGGACGTCACTGCGGATTCGGAAAGCGTAAGGGTACTGCGAACGCCCGCATGCCTACCAAGCTGCTGTGGA TGCAGCGCCAGCGCGTTCTGCGCCGCCTGTTGAAGAAGTACCGCGACAGCAAGAAGATTGACAGGCACCTGTACCACGAC CTGTACATGAAGTGCAAGGGTAACGTATTCAAGAACAAGCGCGTCCTCATGGAGTACATCCACAAGAAGAAGGCTGAGAA GCAGCGCAGCAAGATGCTGGCTGATCAGGCCGAGGCTCGCCGACAGAAGGTGCGTGAGGCCCGCAAGCGCCGAGAGGAGC GTATTGCCACCACAGAGCAGGAGCTCATCGCCCTGCATGCTAAGGAGGACGAGATCGCTGCCAAGGCCGCCACCGCGGGT CACTAAGCAGTCCGACCTCGCTAGTCGAGGAACTCCATATTG
Cloned cDNAs prepared from polyadenylated RNA isolated from adult heads.
For the RH cDNA library, adult heads were collected from an isogenic y; cn bw sp (iso-1) strain.
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., Genomics 37: 327-336). A linker was then ligated to the single-strand cDNA following the published protocol (Shibata, Y., et al., Biotechniques, in press). Subsequently, the cDNA was normalized by using RoT=1.0 as published (Carninci, P., et al., Genome Res. 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, thecDNA was cloned in the lambda FLC-I vector. Subsequently, the library was bulk-excised into pFLC-I plasmid as described (Carninci, P., et al., Genomics, 2001, 77:79-90 ). cDNAs were transformed into DH5-alpha TonA strain.