Kawasawa Yuka, McKenzie Louise M, Hill David P, Bono Hidemasa, Yanagisawa Masashi
Howard Hughes Medical Institute, Department of Molecular Genetics, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9050, USA.
Genome Res. 2003 Jun;13(6B):1466-77. doi: 10.1101/gr.1087603.
G protein-coupled receptors (GPCRs) comprise the largest family of receptor proteins in mammals and play important roles in many physiological and pathological processes. Gene expression of GPCRs is temporally and spatially regulated, and many splicing variants are also described. In many instances, different expression profiles of GPCR gene are accountable for the changes of its biological function. Therefore, it is intriguing to assess the complexity of the transcriptome of GPCRs in various mammalian organs. In this study, we took advantage of the FANTOM2 (Functional Annotation Meeting of Mouse cDNA 2) project, which aimed to collect full-length cDNAs inclusively from mouse tissues, and found 410 candidate GPCR cDNAs. Clustering of these clones into transcriptional units (TUs) reduced this number to 213. Out of these, 165 genes were represented within the known 308 GPCRs in the Mouse Genome Informatics (MGI) resource. The remaining 48 genes were new to mouse, and 14 of them had no clear mammalian ortholog. To dissect the detailed characteristics of each transcript, tissue distribution pattern and alternative splicing were also ascertained. We found many splicing variants of GPCRs that may have a relevance to disease occurrence. In addition, the difficulty in cloning tissue-specific and infrequently transcribed GPCRs is discussed further.
G蛋白偶联受体(GPCRs)是哺乳动物中最大的受体蛋白家族,在许多生理和病理过程中发挥着重要作用。GPCRs的基因表达在时间和空间上受到调控,并且还发现了许多剪接变体。在许多情况下,GPCR基因不同的表达谱决定了其生物学功能的变化。因此,评估各种哺乳动物器官中GPCRs转录组的复杂性很有意思。在本研究中,我们利用了FANTOM2(小鼠cDNA 2功能注释会议)项目,该项目旨在全面收集小鼠组织中的全长cDNA,并发现了410个候选GPCR cDNA。将这些克隆聚类为转录单元(TUs)后,数量减少到213个。其中,165个基因在小鼠基因组信息学(MGI)资源中已知的308个GPCRs中有所体现。其余48个基因对小鼠来说是新的,其中14个没有明确的哺乳动物直系同源基因。为了剖析每个转录本的详细特征,还确定了组织分布模式和可变剪接。我们发现了许多可能与疾病发生相关的GPCRs剪接变体。此外,还进一步讨论了克隆组织特异性和转录不频繁的GPCRs的困难。