Phillips R L, Ernst R E, Brunk B, Ivanova N, Mahan M A, Deanehan J K, Moore K A, Overton G C, Lemischka I R
Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Science. 2000 Jun 2;288(5471):1635-40. doi: 10.1126/science.288.5471.1635.
Blood cell production originates from a rare population of multipotent, self-renewing stem cells. A genome-wide gene expression analysis was performed in order to define regulatory pathways in stem cells as well as their global genetic program. Subtracted complementary DNA libraries from highly purified murine fetal liver stem cells were analyzed with bioinformatic and array hybridization strategies. A large percentage of the several thousand gene products that have been characterized correspond to previously undescribed molecules with properties suggestive of regulatory functions. The complete data, available in a biological process-oriented database, represent the molecular phenotype of the hematopoietic stem cell.
血细胞生成源于一群罕见的多能、自我更新干细胞。为了确定干细胞中的调控途径及其整体遗传程序,进行了全基因组基因表达分析。采用生物信息学和阵列杂交策略,对来自高度纯化的小鼠胎儿肝脏干细胞的消减互补DNA文库进行了分析。已鉴定的数千种基因产物中,很大一部分对应于先前未描述的分子,这些分子具有提示调控功能的特性。完整的数据可在一个以生物过程为导向的数据库中获取,代表了造血干细胞的分子表型。