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Cloning Full-Length, Cap-Trapper-Selected cDNAs by Using the Single-Strand Linker Ligation Method
Author(s) -
Yûkô Shibata,
Piero Carninci,
Akira Watahiki,
Toshiyuki Shiraki,
Hiroyuki Konno,
Masami Muramatsu,
Yoshihide Hayashizaki
Publication year - 2001
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/01306st01
Subject(s) - complementary dna , linker , dna ligase , ligation , microbiology and biotechnology , biology , cloning (programming) , dna , untranslated region , dna ligases , genetics , rna , gene , computer science , programming language , operating system
We have developed the single-strand linker ligation method (SSLLM), which uses DNA ligase to add a dsDNA linker to single-stranded (ss) full-length cDNA. The linkers have random 6-bp (dN6 or dGN5) 3' overhangs that can ligate to any cDNA sequence, thereby facilitating the production of cDNA libraries with titers exceeding 1 x 10(6) independent clones. We confirmed that the 5' ends of cDNA inserts cloned by using SSLLM are full-length and include the 5' untranslated regions. The great advantage of our method is that the elimination of the GC tail simplifies the sequencing and protein translation of the full-length clones. Further, our method tags ss cDNAs more efficiently than does the traditional RNA ligase reaction.

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