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果蝇中转录剪接的全局分析。

Global analysis of trans-splicing in Drosophila.

机构信息

Department of Genetics and Developmental Biology, University of Connecticut Stem Cell Institute, University of Connecticut Health Center, Farmington, CT 06030-3301, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Jul 20;107(29):12975-9. doi: 10.1073/pnas.1007586107. Epub 2010 Jul 1.

Abstract

Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and trans-splicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes.

摘要

前体信使 RNA(pre-mRNA)剪接可以将单个 pre-mRNA(顺式)或分离的 pre-mRNAs(反式)上的外显子连接起来。反式剪接在蛋白质编码外显子之间非常罕见,仅在两个果蝇基因中得到证实:mod(mdg4)和 lola。也有人认为,反式剪接是产生包含来自多个遥远基因组位点的序列的嵌合 RNA 产物的一种机制。由于大多数高通量方法无法区分顺式和反式剪接事件,因此任何生物体中蛋白质编码外显子之间反式剪接发生的程度尚不清楚。在这里,我们使用 mRNA 的配对末端深度测序来鉴定在果蝇种间杂种中经历反式剪接的基因。我们没有观察到可信的证据表明存在由来自远距离基因组位点转录的 RNA 反式剪接产生的嵌合 RNA。相反,我们的数据表明,实验假象是大多数(如果不是全部)明显的嵌合 RNA 产物的来源。然而,我们确实鉴定了 80 个似乎在同源等位基因之间经历反式剪接的基因,并可以根据其组织分为三类:(i)具有多个 3'末端外显子的基因,(ii)具有多个第一外显子的基因,和(iii)具有非常大内含子的基因,通常包含其他基因。我们的结果表明,在果蝇中,同源等位基因之间的反式剪接比以前认为的更为常见,并且可能有助于结构复杂基因的表达。

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Global analysis of trans-splicing in Drosophila.果蝇中转录剪接的全局分析。
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