Fu Yonggui, Ge Yutong, Sun Yu, Liang Jiahui, Wan Liang, Wu Xiaojian, Xu Anlong
Shenzhen Research Center of State Key Laboratory for Biocontrol, Research Institute of Sun Yat-sen University at Shenzhen, Shenzhen Virtual University Park, Hi-tech Industrial Park, Nanshan District, Shenzhen, 518057, P. R. China.
State Key Laboratory for Biocontrol, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, Department of Biochemistry, School of Life Sciences, Sun Yat-sen University, Higher Education Mega Center, Guangzhou, 510006, P. R. China.
PLoS One. 2015 Dec 28;10(12):e0145477. doi: 10.1371/journal.pone.0145477. eCollection 2015.
Gene transcribing with alternative polyadenylation (APA) sites leads to mRNA isoforms, which may encode different proteins or harbor different 3'UTRs. APA plays an important role in regulating gene expression network among various physiological processes, such as development, immune responses and cancer. Several methods of library construction for APA study have been developed to apply high-throughput sequencing. However, the requirement of high-input RNA and time-consuming nature of the current methods limited the studies of APA for the samples difficult to obtain. Here, we describe a new method based on our SAPAS in combining in vitro transcription (IVT) and magnetic beads purification. The new IVT-SAPAS provides a rapid and high-parallel procedure for APA library construction with low-input sample, which may be a new robust approach for studying APA.
具有可变聚腺苷酸化(APA)位点的基因转录会产生mRNA异构体,这些异构体可能编码不同的蛋白质或含有不同的3'非翻译区(3'UTR)。APA在调节各种生理过程(如发育、免疫反应和癌症)中的基因表达网络中起着重要作用。为了应用高通量测序,已经开发了几种用于APA研究的文库构建方法。然而,当前方法对高输入RNA的要求以及耗时的特性限制了对难以获得的样本进行APA研究。在此,我们描述了一种基于我们的SAPAS并结合体外转录(IVT)和磁珠纯化的新方法。新的IVT-SAPAS为低输入样本的APA文库构建提供了一种快速且高度并行的程序,这可能是研究APA的一种新的强大方法。