Construction of a human full-length cDNA bank

We aimed to construct a full-length cDNA bank from an entire set of human genes and to analyze the function of a protein encoded by each cDNA. To achieve this purpose, a multifunctional phagemid shuttle vector, pKAl, was constructed for preparing a high-quality cDNA library composed of full-length c...

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Veröffentlicht in:Gene 1994, Vol.150 (2), p.243-250
Hauptverfasser: Seishi, Kato, Shingo, Sekine, Su-Wan, Oh, Nam-Soon, Kim, Yuri, Umezawa, Naoto, Abe, Midori, Yokoyama-Kobayashi, Takashi, Aoki
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Sprache:eng
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Zusammenfassung:We aimed to construct a full-length cDNA bank from an entire set of human genes and to analyze the function of a protein encoded by each cDNA. To achieve this purpose, a multifunctional phagemid shuttle vector, pKAl, was constructed for preparing a high-quality cDNA library composed of full-length cDNA clones which can be sequenced and expressed in vitro and in mammalian cells without subcloning the cDNA fragment into other vectors. Using this as a vector primer, we have prepared a prototype of the bank composed of full-length cDNAs encoding 236 human proteins whose amino acid sequences are identical or similar to known proteins. Most cDNAs contain a putative cap site sequence, some of which show a pyrimidine-rich conserved sequence exhibiting polymorphism. It was confirmed that the vector permits efficient in vitro translation, expression in mammalian cells and the preparation of nested deletion mutants.
ISSN:0378-1119
1879-0038
DOI:10.1016/0378-1119(94)90433-2