Molecular Cancer Biology Program, Duke University Medical Center, Durham, North Carolina 27710, USA.
RNA. 2012 Aug;18(8):1435-45. doi: 10.1261/rna.033621.112. Epub 2012 Jun 26.
The key postulate that one gene encodes one protein has been overhauled with the discovery that one gene can generate multiple RNA transcripts through alternative mRNA processing. In this study, we describe SplicerEX, a novel and uniquely motivated algorithm designed for experimental biologists that (1) detects widespread changes in mRNA isoforms from both conventional and splice sensitive microarray data, (2) automatically categorizes mechanistic changes in mRNA processing, and (3) mitigates known technological artifacts of exon array-based detection of alternative splicing resulting from 5' and 3' signal attenuation, background detection limits, and saturation of probe set signal intensity. In this study, we used SplicerEX to compare conventional and exon-based Affymetrix microarray data in a model of EBV transformation of primary human B cells. We demonstrated superior detection of 3'-located changes in mRNA processing by the Affymetrix U133 GeneChip relative to the Human Exon Array. SplicerEX-identified exon-level changes in the EBV infection model were confirmed by RT-PCR and revealed a novel set of EBV-regulated mRNA isoform changes in caspases 6, 7, and 8. Finally, SplicerEX as compared with MiDAS analysis of publicly available microarray data provided more efficiently categorized mRNA isoform changes with a significantly higher proportion of hits supported by previously annotated alternative processing events. Therefore, SplicerEX provides an important tool for the biologist interested in studying changes in mRNA isoform usage from conventional or splice-sensitive microarray platforms, especially considering the expansive amount of archival microarray data generated over the past decade. SplicerEX is freely available upon request.
一个基因编码一种蛋白质的关键假设已经被推翻,因为人们发现一个基因可以通过选择性的 mRNA 加工生成多个 RNA 转录本。在这项研究中,我们描述了 SplicerEX,这是一种新颖的、专门为实验生物学家设计的算法,它 (1) 从常规和拼接敏感的微阵列数据中检测 mRNA 异构体的广泛变化,(2) 自动分类 mRNA 处理的机制变化,以及 (3) 减轻基于外显子阵列的替代拼接检测中已知的技术伪影,这些伪影是由 5'和 3'信号衰减、背景检测限和探针集信号强度饱和引起的。在这项研究中,我们使用 SplicerEX 比较了 EBV 转化原代人 B 细胞的模型中的常规和基于外显子的 Affymetrix 微阵列数据。我们证明了 Affymetrix U133 GeneChip 在检测 mRNA 加工 3' 位置的变化方面优于 Human Exon Array。SplicerEX 鉴定的 EBV 感染模型中外显子水平的变化通过 RT-PCR 得到了证实,并揭示了一组新的 EBV 调节的 caspase 6、7 和 8 的 mRNA 异构体变化。最后,与 MiDAS 对公共微阵列数据的分析相比,SplicerEX 提供了更有效地分类 mRNA 异构体变化的方法,并且有更高比例的命中得到了先前注释的替代处理事件的支持。因此,SplicerEX 为有兴趣从常规或拼接敏感的微阵列平台研究 mRNA 异构体使用变化的生物学家提供了一个重要的工具,尤其是考虑到过去十年中生成的大量存档微阵列数据。SplicerEX 可根据要求免费提供。