Systematic sequencing of cDNA clones using the transposon Tn5

被引:51
作者
Shevchenko, Y
Bouffard, GG
Butterfield, YSN
Blakesley, RW
Hartley, JL
Young, AC
Marra, MA
Jones, SJM
Touchman, JW
Green, ED
机构
[1] NIH, Intramural Sequencing Ctr, Gaithersburg, MD 20877 USA
[2] NHGRI, Genome Technol Branch, Bethesda, MD 20892 USA
[3] British Columbia Canc Agcy, Genome Sci Ctr, Vancouver, BC V5Z 4E6, Canada
[4] Invitrogen Corp, Rockville, MD 20850 USA
关键词
D O I
10.1093/nar/30.11.2469
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In parallel with the production of genomic sequence data, attention is being focused on the generation of comprehensive cDNA-sequence resources. Such efforts are increasingly emphasizing the production of high-accuracy sequence corresponding to the entire insert of cDNA clones, especially those presumed to reflect the full-length mRNA. The complete sequencing of cDNA clones on a large scale presents unique challenges because of the generally small, yet heterogeneous, sizes of the cloned inserts. We have developed a strategy for high-throughput sequencing of cDNA clones using the transposon Tn5. This approach has been tailored for implementation within an existing large-scale 'shotgun-style' sequencing program, although it could be readily adapted for use in virtually any sequencing environment. In addition, we have developed a modified version of our strategy that can be applied to cDNA clones with large cloning vectors, thereby overcoming a potential limitation of transposon-based approaches. Here we describe the details of our cDNA-sequencing pipeline, including a summary of the experience in sequencing more than 4200 cDNA clones to produce more than 8 million base pairs of high-accuracy cDNA sequence. These data provide both convincing evidence that the insertion of Tn5 into cDNA clones is sufficiently random for its effective use in large-scale cDNA sequencing as well as interesting insight about the sequence context preferred for insertion by Tn5.
引用
收藏
页码:2469 / 2477
页数:9
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