Balanced-size and long-size cloning of full-length, cap-trapped cDNAs into vectors of the novel λ-FLC family allows enhanced gene discovery rate and functional analysis

被引:58
作者
Carninci, P
Shibata, Y
Hayatsu, N
Itoh, M
Shiraki, T
Hirozane, T
Watahiki, A
Shibata, K
Konno, H
Muramatsu, M
Hayashizaki, Y
机构
[1] RIKEN Genom Sci Ctr, Genome Explorat Res Grp, Tsurumi Ku, Kanagawa 2300045, Japan
[2] RIKEN Tsukuba Inst, Genome Sci Lab, Tsukuba, Ibaraki 3050074, Japan
[3] Univ Tsukuba, Inst Basic Med Sci, Tsukuba, Ibaraki 3058577, Japan
关键词
full-length cDNA; cloning vector; function vector; normalization and subtraction; gene discovery;
D O I
10.1006/geno.2001.6601
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have developed a new class of cloning vectors: lambda -full-length cDNA (lambda -FLC) cloning vectors. These vectors can be bulk-excised for preparing full-length cDNA libraries in which a high proportion of the plasmids carry large inserts that can be transferred into other (for example, functional) vectors. Unlike other cloning vectors, lambda -FLC vectors accommodate a broad range of sizes of eukaryotic cDNA inserts because they contain "size balancers." Further, the main protocol we use for direct bulk excision of plasmids is mediated by a Cre-lox system and is apparently free of size bias. The average size of the inserts from excised plasmid cDNA libraries was 2.9 kb for standard and 6.9 kb for size-selected cDNA. The average insert size of the full-length cDNA libraries was correlated to the rate of new gene discovery, suggesting that effectively cloning rarely expressed mRNAs requires vectors that can accommodate large inserts from a variety of sources. Part of the vectors are also suitable for bulk transfer of inserts into various functional vectors.
引用
收藏
页码:79 / 90
页数:12
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