Cheng L, Li L
Centers for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
Department of Medical and Molecular Genetics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
CPT Pharmacometrics Syst Pharmacol. 2016 Nov;5(11):588-598. doi: 10.1002/psp4.12107. Epub 2016 Oct 31.
The Library of Integrated Cellular Signatures (LINCS) project provides comprehensive transcriptome profiling of human cell lines before and after chemical and genetic perturbations. Its L1000 platform utilizes 978 landmark genes to infer the transcript levels of 14,292 genes computationally. Here we conducted the L1000 data quality control analysis by using MCF7, PC3, and A375 cell lines as representative examples. Before perturbations, a promising 80% correlation in transcriptome was observed between L1000- and Affymetrix HU133A-platforms. After library-based shRNA perturbations, a moderate 30% of differentially expressed genes overlapped between any two selected controls viral vectors using the L1000 platform. The mitogen-activated protein kinase, vascular endothelial growth factor, and T-cell receptor pathways were identified as the most significantly shared pathways between chemical and genetic perturbations in cancer cells. In conclusion, L1000 platform is reliable in assessing transcriptome before perturbation. Its response to perturbagens needs to be interpreted with caution. A quality control analysis pipeline of L1000 is recommended before addressing biological questions.
综合细胞信号库(LINCS)项目提供了化学和基因扰动前后人类细胞系的全面转录组分析。其L1000平台利用978个标志性基因通过计算推断14292个基因的转录水平。在此,我们以MCF7、PC3和A375细胞系为代表进行了L1000数据质量控制分析。在扰动之前,L1000平台与Affymetrix HU133A平台之间在转录组方面观察到有前景的80%的相关性。在基于文库的shRNA扰动之后,使用L1000平台时,任意两个选定的对照病毒载体之间有30%的中度差异表达基因重叠。丝裂原活化蛋白激酶、血管内皮生长因子和T细胞受体途径被确定为癌细胞化学和基因扰动之间最显著的共同途径。总之,L1000平台在评估扰动前的转录组方面是可靠的。其对扰动剂的反应需要谨慎解读。建议在解决生物学问题之前建立L1000的质量控制分析流程。