Kawaji Hideya, Severin Jessica, Lizio Marina, Forrest Alistair R R, van Nimwegen Erik, Rehli Michael, Schroder Kate, Irvine Katharine, Suzuki Harukazu, Carninci Piero, Hayashizaki Yoshihide, Daub Carsten O
RIKEN Omics Science Center, RIKEN Yokohama Institute, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama City, Kanagawa 230-0045, Japan.
Nucleic Acids Res. 2011 Jan;39(Database issue):D856-60. doi: 10.1093/nar/gkq1112. Epub 2010 Nov 12.
The international Functional Annotation Of the Mammalian Genomes 4 (FANTOM4) research collaboration set out to better understand the transcriptional network that regulates macrophage differentiation and to uncover novel components of the transcriptome employing a series of high-throughput experiments. The primary and unique technique is cap analysis of gene expression (CAGE), sequencing mRNA 5'-ends with a second-generation sequencer to quantify promoter activities even in the absence of gene annotation. Additional genome-wide experiments complement the setup including short RNA sequencing, microarray gene expression profiling on large-scale perturbation experiments and ChIP-chip for epigenetic marks and transcription factors. All the experiments are performed in a differentiation time course of the THP-1 human leukemic cell line. Furthermore, we performed a large-scale mammalian two-hybrid (M2H) assay between transcription factors and monitored their expression profile across human and mouse tissues with qRT-PCR to address combinatorial effects of regulation by transcription factors. These interdependent data have been analyzed individually and in combination with each other and are published in related but distinct papers. We provide all data together with systematic annotation in an integrated view as resource for the scientific community (http://fantom.gsc.riken.jp/4/). Additionally, we assembled a rich set of derived analysis results including published predicted and validated regulatory interactions. Here we introduce the resource and its update after the initial release.
国际哺乳动物基因组功能注释4(FANTOM4)研究合作旨在通过一系列高通量实验更好地理解调节巨噬细胞分化的转录网络,并发现转录组的新成分。主要且独特的技术是基因表达帽分析(CAGE),即使用第二代测序仪对mRNA的5'端进行测序,即使在没有基因注释的情况下也能定量启动子活性。其他全基因组实验对该设置进行补充,包括短RNA测序、大规模扰动实验的微阵列基因表达谱分析以及用于表观遗传标记和转录因子的芯片免疫沉淀分析(ChIP-chip)。所有实验均在THP-1人白血病细胞系的分化时间进程中进行。此外,我们在转录因子之间进行了大规模的哺乳动物双杂交(M2H)分析,并用qRT-PCR监测它们在人和小鼠组织中的表达谱,以研究转录因子调控的组合效应。这些相互依赖的数据已分别进行分析,并相互结合,发表在相关但不同的论文中。我们将所有数据与系统注释一起以综合视图提供,作为科学界的资源(http://fantom.gsc.riken.jp/4/)。此外,我们汇总了一组丰富的衍生分析结果,包括已发表的预测和验证的调控相互作用。在此我们介绍该资源及其初始发布后的更新情况。