Symula Derek J, Zhu Yiwen, Schimenti John C, Rubin Edward M
Genome Sciences Department, Lawrence Berkeley National Lab, Berkeley, California, 94720, USA.
Mamm Genome. 2004 Jan;15(1):1-13. doi: 10.1007/s00335-002-2228-x.
Expression profiling offers a potential high-throughput phenotype screen for mutant mouse embryonic stem (ES) cells. We have assessed the ability of expression arrays to distinguish among heterozygous mutant ES cell lines and to accurately reflect the normal function of the mutated genes. Two ES cell lines hemizygous for overlapping regions of mouse Chromosome (Chr) 5 differed substantially from the wildtype parental line and from each other. Expression differences included frequent downregulation of hemizygous genes and downstream effects on genes mapping to other chromosomes. Some genes were affected similarly in each deletion line, consistent with the overlap of the deletions. To determine whether such downstream effects reveal pathways impacted by a mutation, we examined ES cell lines heterozygous for mutations in either of two well-characterized genes. A heterozygous mutation in the gene encoding the cell cycle regulator, cyclin D kinase 4 ( Cdk4), affected expression of many genes involved in cell growth and proliferation. A heterozygous mutation in the ATP binding cassette transporter family A, member 1 ( Abca1) gene, altered genes associated with lipid homeostasis, the cytoskeleton, and vesicle trafficking. Heterozygous Abca1 mutation had similar effects in liver, indicating that ES cell expression profile reflects changes in fundamental processes relevant to mutant gene function in multiple cell types.
表达谱分析为突变小鼠胚胎干细胞(ES细胞)提供了一种潜在的高通量表型筛选方法。我们评估了表达阵列区分杂合突变ES细胞系以及准确反映突变基因正常功能的能力。两个小鼠5号染色体(Chr)重叠区域半合子的ES细胞系与野生型亲代细胞系以及彼此之间存在显著差异。表达差异包括半合子基因的频繁下调以及对映射到其他染色体上的基因的下游影响。在每个缺失系中,一些基因受到类似影响,这与缺失的重叠情况一致。为了确定这种下游效应是否揭示了受突变影响的途径,我们检查了两个特征明确的基因中任一基因发生突变的杂合ES细胞系。编码细胞周期调节因子细胞周期蛋白D激酶4(Cdk4)的基因中的杂合突变影响了许多参与细胞生长和增殖的基因的表达。ATP结合盒转运蛋白家族A成员1(Abca1)基因中的杂合突变改变了与脂质稳态、细胞骨架和囊泡运输相关的基因。杂合Abca1突变在肝脏中具有类似作用,表明ES细胞表达谱反映了多种细胞类型中与突变基因功能相关的基本过程的变化。