Yeo Gene W, Xu Xiangdong, Liang Tiffany Y, Muotri Alysson R, Carson Christian T, Coufal Nicole G, Gage Fred H
Crick-Jacobs Center for Theoretical and Computational Biology, Salk Institute, La Jolla, California, USA.
PLoS Comput Biol. 2007 Oct;3(10):1951-67. doi: 10.1371/journal.pcbi.0030196. Epub 2007 Aug 24.
Human embryonic stem cells (hESCs) and neural progenitor (NP) cells are excellent models for recapitulating early neuronal development in vitro, and are key to establishing strategies for the treatment of degenerative disorders. While much effort had been undertaken to analyze transcriptional and epigenetic differences during the transition of hESC to NP, very little work has been performed to understand post-transcriptional changes during neuronal differentiation. Alternative RNA splicing (AS), a major form of post-transcriptional gene regulation, is important in mammalian development and neuronal function. Human ESC, hESC-derived NP, and human central nervous system stem cells were compared using Affymetrix exon arrays. We introduced an outlier detection approach, REAP (Regression-based Exon Array Protocol), to identify 1,737 internal exons that are predicted to undergo AS in NP compared to hESC. Experimental validation of REAP-predicted AS events indicated a threshold-dependent sensitivity ranging from 56% to 69%, at a specificity of 77% to 96%. REAP predictions significantly overlapped sets of alternative events identified using expressed sequence tags and evolutionarily conserved AS events. Our results also reveal that focusing on differentially expressed genes between hESC and NP will overlook 14% of potential AS genes. In addition, we found that REAP predictions are enriched in genes encoding serine/threonine kinase and helicase activities. An example is a REAP-predicted alternative exon in the SLK (serine/threonine kinase 2) gene that is differentially included in hESC, but skipped in NP as well as in other differentiated tissues. Lastly, comparative sequence analysis revealed conserved intronic cis-regulatory elements such as the FOX1/2 binding site GCAUG as being proximal to candidate AS exons, suggesting that FOX1/2 may participate in the regulation of AS in NP and hESC. In summary, a new methodology for exon array analysis was introduced, leading to new insights into the complexity of AS in human embryonic stem cells and their transition to neural stem cells.
人类胚胎干细胞(hESCs)和神经祖细胞(NP)是在体外重现早期神经元发育的优秀模型,也是建立退行性疾病治疗策略的关键。尽管人们已经付出很多努力来分析hESC向NP转变过程中的转录和表观遗传差异,但对于理解神经元分化过程中的转录后变化却鲜有研究。可变RNA剪接(AS)是转录后基因调控的主要形式,在哺乳动物发育和神经元功能中起着重要作用。我们使用Affymetrix外显子阵列对人类胚胎干细胞、hESC衍生的NP和人类中枢神经系统干细胞进行了比较。我们引入了一种异常值检测方法,即基于回归的外显子阵列协议(REAP),以识别与hESC相比预计在NP中发生AS的1737个内部外显子。对REAP预测的AS事件进行实验验证,结果表明在特异性为77%至96%的情况下,阈值依赖性灵敏度范围为56%至69%。REAP预测与使用表达序列标签鉴定的可变事件集以及进化保守的AS事件有显著重叠。我们的结果还表明,关注hESC和NP之间差异表达的基因会忽略14%的潜在AS基因。此外,我们发现REAP预测在编码丝氨酸/苏氨酸激酶和解旋酶活性的基因中富集。一个例子是REAP预测的SLK(丝氨酸/苏氨酸激酶2)基因中的一个可变外显子,它在hESC中差异包含,但在NP以及其他分化组织中被跳过。最后,比较序列分析揭示了保守的内含子顺式调控元件,如靠近候选AS外显子的FOX1/2结合位点GCAUG,这表明FOX1/2可能参与NP和hESC中AS的调控。总之,我们引入了一种新的外显子阵列分析方法,从而对人类胚胎干细胞中AS的复杂性及其向神经干细胞的转变有了新的认识。