Burdon T, Sankaran L, Wall R J, Spencer M, Hennighausen L
Laboratory of Biochemistry and Metabolism, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1991 Apr 15;266(11):6909-14.
Expression of the mouse whey acidic protein (WAP) gene is specific to the mammary gland, is induced several thousand-fold during pregnancy, and is under the control of steroid and peptide hormones. To study developmental regulation of the mouse WAP gene, a 7.2-kilobase (kb) WAP transgene, including 2.6 kb of 5'- and 1.6 kb of 3'-flanking sequences, was introduced into mice. Of the 13 lines of mice examined, 6 expressed the transgenes during lactation at levels between 3 and 54% of the endogenous gene. Although expression was dependent on the site of integration, the transgenes within a given locus were expressed in a copy number-dependent manner and were coordinately regulated. The WAP transgenes were expressed specifically in the mammary gland, but showed a deregulated pattern of expression during mammary development. In all six lines of mice, induction of the WAP transgenes during pregnancy preceded that of the endogenous gene. During lactation, expression in two lines increased coordinately with the endogenous gene, and in three other lines of mice, transgene expression decreased to a basal level. These data indicate that the 7.2-kb gene contains some but not all of the elements necessary for correct developmental regulation. At a functional level it appears as if a repressor element, which inactivates the endogenous gene until late pregnancy, and an element necessary for induction during lactation are absent from the transgene. Complementary results from developmental and hormone induction studies suggest that WAP gene expression during pregnancy and lactation is mediated by different mechanisms.
小鼠乳清酸性蛋白(WAP)基因的表达具有乳腺特异性,在孕期可被诱导数千倍,且受类固醇和肽类激素调控。为研究小鼠WAP基因的发育调控,将一个7.2千碱基(kb)的WAP转基因(包括2.6 kb的5'侧翼序列和1.6 kb的3'侧翼序列)导入小鼠体内。在所检测的13个小鼠品系中,有6个品系在泌乳期表达该转基因,表达水平为内源基因的3%至54%。尽管表达依赖于整合位点,但给定基因座内的转基因以拷贝数依赖的方式表达且受到协同调控。WAP转基因在乳腺中特异性表达,但在乳腺发育过程中表现出表达失调的模式。在所有6个小鼠品系中,孕期WAP转基因的诱导先于内源基因。在泌乳期,两个品系中的表达与内源基因协同增加,而在另外三个小鼠品系中,转基因表达降至基础水平。这些数据表明,7.2 kb的基因包含了正确发育调控所需的部分而非全部元件。在功能层面,转基因似乎缺少一种在妊娠晚期之前使内源基因失活的阻遏元件以及泌乳期诱导所需的元件。发育和激素诱导研究的互补结果表明,孕期和泌乳期WAP基因的表达由不同机制介导。