Jochheim Andrea, Cieslak Alexandra, Hillemann Tina, Cantz Tobias, Scharf Jennifer, Manns Michael P, Ott Michael
Hannover Medical School, Centre of Internal Medicine, Department of Gastroenterology, Hepatology and Endocrinology, Carl-Neubergstr 1, 30625 Hannover, Germany.
Differentiation. 2003 Jan;71(1):62-72. doi: 10.1046/j.1432-0436.2003.700606.x.
The development of a complex organ such as the liver relies on precise temporal and spatial gene expression patterns during ontogenesis. The unique adult phenotype is a result of a cascade of transcriptional events that finally trigger gene expression in a liver-specific fashion. Development in mice starts at embryonic stage E8.5-9.5 with the expression of several genes typically associated with liver tissue. While the role of some genes and their expression is well studied, little is known about the complex expression pattern changes during embryonic and fetal liver development. High-density oligonucleotide microarrays, which allow simultaneous expression analysis of 12,488 mouse mRNA transcripts and EST sequences, were used to study the gene expression profiles in day 7.5 embryonic tissue, in micro-dissected fetal liver tissue from day 11.5 and day 13.5 embryos, and in adult liver. In pairwise comparisons of all stages, a total of 4242 distinct genes or ESTs were found to be differentially regulated. Cross-comparisons of data from all stages detected the highest number of differentially regulated genes in E11.5 fetal liver tissue versus adult liver (3063 genes) and the lowest number in E11.5 versus E13.5 fetal liver tissue (517 genes). Using adult liver as reference tissue, 212 genes were regulated exclusively in E7.5 embryonic tissue, 303 genes in E11.5 and 198 in E13.5 fetal liver tissue. Expression profiles of the 31 genes with significant regulation at all stages as well as of a number of known developmentally regulated genes were compared with published results and interpreted. The gene expression profiles detected by microarray hybridization were independently confirmed for selected genes by quantitative RT-PCR. Our data presented here suggest that a relatively small number of stage-specific genes exist, which may be of particular importance for liver development, growth and differentiation. Furthermore, the microarray approach led to the identification of a number of genes, which have not yet been associated with liver organogenesis and maturation.
诸如肝脏这样的复杂器官的发育依赖于个体发育过程中精确的时空基因表达模式。独特的成年表型是一系列转录事件的结果,这些事件最终以肝脏特异性的方式触发基因表达。小鼠的发育始于胚胎阶段E8.5 - 9.5,此时一些通常与肝脏组织相关的基因开始表达。虽然一些基因的作用及其表达已得到充分研究,但对于胚胎和胎儿肝脏发育过程中复杂的表达模式变化却知之甚少。高密度寡核苷酸微阵列可同时对12488个小鼠mRNA转录本和EST序列进行表达分析,被用于研究第7.5天胚胎组织、第11.5天和第13.5天胚胎的显微切割胎儿肝脏组织以及成年肝脏中的基因表达谱。在所有阶段的成对比较中,共发现4242个不同的基因或ESTs受到差异调节。对所有阶段的数据进行交叉比较发现,E11.5胎儿肝脏组织与成年肝脏之间差异调节基因的数量最多(3063个基因),而E11.5与E13.5胎儿肝脏组织之间差异调节基因的数量最少(517个基因)。以成年肝脏作为参照组织,分别有212个基因仅在E7.5胚胎组织中受到调节,303个基因在E11.5中受到调节,198个基因在E13.5胎儿肝脏组织中受到调节。将在所有阶段均有显著调节的31个基因以及一些已知的发育调节基因的表达谱与已发表的结果进行比较并加以解读。通过微阵列杂交检测到的基因表达谱通过定量RT-PCR对选定基因进行了独立验证。我们在此展示的数据表明,存在相对少量的阶段特异性基因,它们可能对肝脏的发育、生长和分化尤为重要。此外,微阵列方法还导致鉴定出了一些尚未与肝脏器官发生和成熟相关联的基因。