Osipovich Anna B, Singh Aparna, Ruley H Earl
Department of Microbiology and Immunology, Vanderbilt University, School of Medicine, Nashville, Tennessee 37232-2363, USA.
Genome Res. 2005 Mar;15(3):428-35. doi: 10.1101/gr.3258105.
Gene trap mutagenesis in mouse embryonic stem cells has been widely used for genome-wide studies of mammalian gene function. However, while large numbers of genes can be disrupted, individual mutations may suffer from limitations due to the structure and/or placement of targeting vector. To extend the utility of gene trap mutagenesis, replaceable 3' [or poly(A)] gene trap vectors were developed that permit sequences inserted in individual entrapment clones to be engineered by Cre-mediated recombination. 3' traps incorporating different drug resistance genes could be readily exchanged, simply by selecting for the drug-resistance gene of the replacement vector. By substituting different 3' traps, we show that otherwise identical fusion genes containing a large first exon (804 nt) are not expressed at appreciably lower levels than genes expressing small first exons (384 and 151 nt). Thus, size appears to have less effect on the expression and processing of first exons than has been reported for internal exons. Finally, a retroviral poly(A) trap (consisting of a RNA polymerase II promoter, a neomycin-resistance gene, and 5'-splice site) typically produced mutagenized clones in which vector sequences spliced to the 3'-terminal exons of cellular transcription units, suggesting strong selection for fusion transcripts that evade nonsense-mediated decay. The efficient exchange of poly(A) traps should greatly extend the utility of mutant libraries generated by gene entrapment and provides new strategies to study the rules that govern the expression of exons inserted throughout the genome.
基因捕获诱变在小鼠胚胎干细胞中已被广泛用于哺乳动物基因功能的全基因组研究。然而,虽然大量基因可被破坏,但由于靶向载体的结构和/或位置,个别突变可能存在局限性。为了扩展基因捕获诱变的效用,开发了可替换的3'[或聚(A)]基因捕获载体,其允许通过Cre介导的重组对插入单个捕获克隆中的序列进行工程改造。仅通过选择替换载体的耐药基因,就可以轻松交换包含不同耐药基因的3'捕获载体。通过替换不同的3'捕获载体,我们发现,否则相同的包含大的第一个外显子(804 nt)的融合基因的表达水平并不明显低于表达小的第一个外显子(384和151 nt)的基因。因此,大小对第一个外显子表达和加工的影响似乎比已报道的内部外显子要小。最后,逆转录病毒聚(A)捕获载体(由RNA聚合酶II启动子、新霉素抗性基因和5'剪接位点组成)通常产生诱变克隆,其中载体序列剪接到细胞转录单位的3'末端外显子,这表明对逃避无义介导衰变的融合转录本有强烈选择。聚(A)捕获载体的有效交换应极大地扩展通过基因捕获产生的突变体文库的效用,并为研究控制整个基因组中插入外显子表达的规则提供新策略。