Li Robert W, Meyer Matthew J, Van Tassell Curtis P, Sonstegard Tad S, Connor Erin E, Van Amburgh Michael E, Boisclair Yves R, Capuco Anthony V
Bovine Functional Genomics Laboratory, United States Department of Agriculture-Agricultural Research Service, Beltsville, Maryland 20705, USA.
Physiol Genomics. 2006 Oct 3;27(1):42-53. doi: 10.1152/physiolgenomics.00032.2006. Epub 2006 Jun 20.
Identification of estrogen-responsive genes is an essential step toward understanding mechanisms of estrogen action during mammary gland development. To identify these genes, 16 prepubertal heifers were used in a 2 x 2 factorial experiment, with ovarian status (intact or ovariectomized) as the first factor and estrogen treatment as the second (control or estradiol). Heifers were ovariectomized at approximately 4.5 mo of age, and estrogen treatments were initiated 1 mo later. After 3 days of treatment, gene expression was analyzed in the parenchyma and fat pad of the bovine mammary gland using a high-density oligonucleotide microarray. Oligonucelotide probes represented 40,808 tentative consensus sequences from TIGR Bos taurus Gene Index and 4,575 singleton expressed sequence tags derived from libraries of pooled mammary gland and gut tissues. Microarray data were analyzed by use of the SAS mixed procedure, with an experiment-wide permutation-based significance level of P < 0.1. Considerable differences in basal gene expression were noted between mammary parenchyma and fat pad. A total of 124 estrogen-responsive genes were identified, with most responding only in the parenchyma or the fat pad. The majority of genes identified were not previously reported to be estrogen responsive. These undoubtedly include genes that are regulated indirectly but also include known estrogen-targeted genes and novel genes with potential estrogen-responsive elements in their promoter regions. The distinctive expression patterns regulated by estrogen in parenchyma and fat pad shed light on the need for both tissues to obtain normal mammary development.
鉴定雌激素反应基因是了解雌激素在乳腺发育过程中作用机制的关键一步。为了鉴定这些基因,16头青春期前的小母牛被用于一项2×2析因实验,其中卵巢状态(完整或去卵巢)作为第一个因素,雌激素处理作为第二个因素(对照或雌二醇)。小母牛在约4.5月龄时进行去卵巢手术,1个月后开始雌激素处理。处理3天后,使用高密度寡核苷酸微阵列分析牛乳腺实质和脂肪垫中的基因表达。寡核苷酸探针代表来自TIGR牛基因索引的40,808个暂定一致性序列以及来自汇集的乳腺和肠道组织文库的4,575个单独特异性表达序列标签。微阵列数据通过SAS混合程序进行分析,全实验基于置换的显著性水平为P < 0.1。在乳腺实质和脂肪垫之间观察到基础基因表达存在显著差异。总共鉴定出124个雌激素反应基因,其中大多数仅在实质或脂肪垫中产生反应。所鉴定的大多数基因以前未被报道为雌激素反应性基因。这些基因无疑包括间接受调控的基因,但也包括已知的雌激素靶向基因以及在其启动子区域具有潜在雌激素反应元件的新基因。雌激素在实质和脂肪垫中调节的独特表达模式揭示了这两种组织对于获得正常乳腺发育的必要性。