Bono Hidemasa, Yagi Ken, Kasukawa Takeya, Nikaido Itoshi, Tominaga Naoko, Miki Rika, Mizuno Yosuke, Tomaru Yasuhiro, Goto Hitoshi, Nitanda Hiroyuki, Shimizu Daisuke, Makino Hirochika, Morita Tomoyuki, Fujiyama Junshin, Sakai Takehito, Shimoji Takashi, Hume David A, Hayashizaki Yoshihide, Okazaki Yasushi
Laboratory for Genome Exploration Research Group, RIKEN Genomic Sciences Center (GSC), RIKEN Yokohama Institute, Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.
Genome Res. 2003 Jun;13(6B):1318-23. doi: 10.1101/gr.1075103.
The number of known mRNA transcripts in the mouse has been greatly expanded by the RIKEN Mouse Gene Encyclopedia project. Validation of their reproducible expression in a tissue is an important contribution to the study of functional genomics. In this report, we determine the expression profile of 57,931 clones on 20 mouse tissues using cDNA microarrays. Of these 57,931 clones, 22,928 clones correspond to the FANTOM2 clone set. The set represents 20,234 transcriptional units (TUs) out of 33,409 TUs in the FANTOM2 set. We identified 7206 separate clones that satisfied stringent criteria for tissue-specific expression. Gene Ontology terms were assigned for these 7206 clones, and the proportion of 'molecular function' ontology for each tissue-specific clone was examined. These data will provide insights into the function of each tissue. Tissue-specific gene expression profiles obtained using our cDNA microarrays were also compared with the data extracted from the GNF Expression Atlas based on Affymetrix microarrays. One major outcome of the RIKEN transcriptome analysis is the identification of numerous nonprotein-coding mRNAs. The expression profile was also used to obtain evidence of expression for putative noncoding RNAs. In addition, 1926 clones (70%) of 2768 clones that were categorized as "unknown EST," and 1969 (58%) clones of 3388 clones that were categorized as "unclassifiable" were also shown to be reproducibly expressed.
日本理化学研究所的小鼠基因百科全书项目极大地扩充了已知的小鼠mRNA转录本数量。验证它们在组织中的可重复表达是对功能基因组学研究的一项重要贡献。在本报告中,我们使用cDNA微阵列确定了20种小鼠组织中57,931个克隆的表达谱。在这57,931个克隆中,22,928个克隆对应于FANTOM2克隆集。该集合代表了FANTOM2集合中33,409个转录单元(TU)中的20,234个转录单元。我们鉴定出7206个满足组织特异性表达严格标准的独立克隆。为这7206个克隆分配了基因本体论术语,并检查了每个组织特异性克隆的“分子功能”本体论比例。这些数据将为各组织的功能提供见解。我们还将使用cDNA微阵列获得的组织特异性基因表达谱与基于Affymetrix微阵列从GNF表达图谱中提取的数据进行了比较。日本理化学研究所转录组分析的一个主要成果是鉴定出大量非蛋白质编码mRNA。该表达谱还用于获得假定非编码RNA的表达证据。此外,被归类为“未知EST”的2768个克隆中的1926个(70%)以及被归类为“无法分类”的3388个克隆中的1969个(58%)也被证明是可重复表达的。