Suzuki Yoshiharu, Nakayama Manabu
Laboratory of Pharmacogenomics, Graduate School of Pharmaceutical Sciences, Chiba University, 2-6-7, Kazusa-kamatari, Chiba 292-0818 Japan.
DNA Res. 2003 Dec 31;10(6):263-75. doi: 10.1093/dnares/10.6.263.
Strain-specific differences in gene expression have been observed among various inbred mouse strains. Two strains that are commonly used in gene-targeting research today are the 129 substrains, which are used to produce ES cell lines, and C57BL/6J, which is used for the extensive backcrosses required to produce isogenic knockout mice. When F2 nonisogenic littermates are assessed using DNA microarrays, one must determine whether the expression profiles obtained resulted either from specific alteration(s) induced by the targeted gene mutation or from gene expression differences related to the genetic background of the parent mouse strains. In the present study, we report the differential expression profile of genes expressed in neonatal brains and adult spleen and liver of 129X1/SvJ and C57BL/6J strains of mice. These comprehensive profiles were assessed using two types of Agilent Mouse Oligo Microarrays (development and standard) and were compiled into a publicly available database. Researchers can use this database to determine whether their microarray findings represent strain-specific differences in gene expression by comparing their data with those cataloged in our database. This database is useful for effectively analyzing DNA microarray data from nonisogenic littermates, and would help researchers avoid time-consuming backcrosses and confirmatory experiments requiring the use of many mice.
在各种近交系小鼠品系中已观察到基因表达的品系特异性差异。如今在基因靶向研究中常用的两个品系是用于产生胚胎干细胞系的129亚系,以及用于产生同基因敲除小鼠所需的广泛回交的C57BL/6J。当使用DNA微阵列评估F2非同源同窝仔时,必须确定获得的表达谱是由靶向基因突变诱导的特定改变导致的,还是由与亲本品系的遗传背景相关的基因表达差异导致的。在本研究中,我们报告了129X1/SvJ和C57BL/6J小鼠品系新生脑以及成年脾脏和肝脏中表达基因的差异表达谱。这些全面的谱图使用两种类型的安捷伦小鼠寡核苷酸微阵列(研发型和标准型)进行评估,并被汇编成一个公开可用的数据库。研究人员可以通过将他们的数据与我们数据库中编目的数据进行比较,使用这个数据库来确定他们的微阵列研究结果是否代表基因表达的品系特异性差异。这个数据库对于有效分析来自非同源同窝仔的DNA微阵列数据很有用,并且将帮助研究人员避免耗时的回交以及需要使用许多小鼠的验证实验。