Kouadjo Kouame E, Nishida Yuichiro, Cadrin-Girard Jean F, Yoshioka Mayumi, St-Amand Jonny
Functional Genomics Laboratory, Molecular Endocrinology and Oncology Research Center, Laval University Medical Center, Department of Anatomy and Physiology, Laval University, Québec, Canada.
BMC Genomics. 2007 May 22;8:127. doi: 10.1186/1471-2164-8-127.
This study aims to characterize the housekeeping and tissue-specific genes in 15 mouse tissues by using the serial analysis of gene expression (SAGE) strategy which indicates the relative level of expression for each transcript matched to the tag.
Here, we identified constantly expressed housekeeping genes, such as eukaryotic translation elongation factor 2, which is expressed in all tissues without significant difference in expression levels. Moreover, most of these genes were not regulated by experimental conditions such as steroid hormones, adrenalectomy and gonadectomy. In addition, we report previously postulated housekeeping genes such as peptidyl-prolyl cis-trans isomerase A, glyceraldehyde-3-phosphate dehydrogenase and beta-actin, which are expressed in all the tissues, but with significant difference in their expression levels. We have also identified genes uniquely detected in each of the 15 tissues and other tissues from public databases.
These identified housekeeping genes could represent appropriate controls for RT-PCR and northern blot when comparing the expression levels of genes in several tissues. The results reveal several tissue-specific genes highly expressed in testis and pituitary gland. Furthermore, the main function of tissue-specific genes expressed in liver, lung and bone is the cell defence, whereas several keratins involved in cell structure function are exclusively detected in skin and vagina. The results from this study can be used for example to target a tissue for agent delivering by using the promoter of tissue-specific genes. Moreover, this study could be used as basis for further researches on physiology and pathology of these tissues.
本研究旨在通过使用基因表达序列分析(SAGE)策略来表征15种小鼠组织中的管家基因和组织特异性基因,该策略可表明与标签匹配的每个转录本的相对表达水平。
在此,我们鉴定出持续表达的管家基因,如真核翻译延伸因子2,它在所有组织中均有表达,且表达水平无显著差异。此外,这些基因中的大多数不受类固醇激素、肾上腺切除术和性腺切除术等实验条件的调控。另外,我们报告了先前假定的管家基因,如肽基脯氨酰顺反异构酶A、甘油醛-3-磷酸脱氢酶和β-肌动蛋白,它们在所有组织中均有表达,但表达水平存在显著差异。我们还从公共数据库中鉴定出了在15种组织中的每一种以及其他组织中独特检测到的基因。
在比较多个组织中基因的表达水平时,这些鉴定出的管家基因可作为逆转录聚合酶链反应(RT-PCR)和Northern印迹的合适对照。结果揭示了在睾丸和垂体中高表达的几种组织特异性基因。此外,在肝脏、肺和骨骼中表达的组织特异性基因的主要功能是细胞防御,而参与细胞结构功能的几种角蛋白仅在皮肤和阴道中检测到。本研究的结果可用于例如通过使用组织特异性基因的启动子来靶向组织进行药物递送。此外,本研究可为这些组织的生理学和病理学的进一步研究提供基础。