ORF-FINDER: a vector for high-throughput gene identification

被引:312
作者
Rombel, IT
Sykes, KF
Rayner, S
Johnston, SA
机构
[1] SW Texas State Univ, Med Ctr, Ctr Biomed Invent, Dept Internal Med, Dallas, TX 75390 USA
[2] SW Texas State Univ, Med Ctr, Ctr Biomed Invent, Dept Biochem, Dallas, TX 75390 USA
关键词
open reading frame; open reading frame selection vector; functional genomic screen; expression library immunization; arasite;
D O I
10.1016/S0378-1119(01)00819-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have developed a simple and efficient system (ORF-FINDER) for selecting open reading frames (ORFs) from randomly fragmented genomic DNA fragments. The ORF-FINDER vectors are plasmids that contain a translational start site out of frame with respect to the gene for green fluorescent protein (GFP). Insertion of DNA fragments that bring the initiating ATG in frame with GFP and that contain no stop codons (that is, ORFs) results in the expression of ORF-GFP fusion proteins. In addition, we have developed software (GeneWorks and GenomeAnalyzer) to predict the optimal insert size for maximizing the number of gene-coding ORFs and minimizing unintentionally selected non-coding ORFs. To demonstrate the feasibility of using the ORF-FINDER system to screen genomes for ORFs, we cloned yeast genomic DNA and succeeded in enriching for ORFs by 25-fold. Furthermore, we have shown that the vector can effectively isolate ORFs from the more complex genomes of eukaryotic parasites. We envision that ORF-FINDER will have several applications including genome sequencing projects, gene building from oligonucleotides and construction of expression libraries enriched for ORFs. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
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