Watson C J, Gordon K E, Robertson M, Clark A J
AFRC Institute of Animal Physiology and Genetics Research, Edinburgh Research Station, Roslin, Midlothian, UK.
Nucleic Acids Res. 1991 Dec 11;19(23):6603-10. doi: 10.1093/nar/19.23.6603.
The minimal 5' regulatory region of the sheep beta-lactoglobulin gene (BLG), as defined in transgenic mice, was used to identify nuclear factors which may be involved in milk protein gene expression in the lactating mammary gland. This 406bp promoter region was dissected into short, overlapping, double-stranded oligonucleotides to facilitate identification of the bound proteins. A variety of sites, for both known and previously undescribed DNA-binding proteins, are occupied in vitro. Some of these factors were investigated in detail. Two forms of nuclear factor I (NFI), which have different recognition site affinities, are present in nuclear extracts from lactating mammary gland and bind to at least 5 sites in this BLG control element. In addition, a factor (milk protein binding factor, MPBF) which is specific to extracts from both mouse and sheep lactating mammary gland binds to 3 BLG promoter sites and may be a milk protein gene transcription factor.
在转基因小鼠中定义的绵羊β-乳球蛋白基因(BLG)的最小5'调控区,被用于鉴定可能参与泌乳乳腺中乳蛋白基因表达的核因子。这个406bp的启动子区域被切割成短的、重叠的双链寡核苷酸,以方便鉴定结合的蛋白质。在体外,已知和先前未描述的DNA结合蛋白的多种位点都被占据。其中一些因子被详细研究。两种具有不同识别位点亲和力的核因子I(NFI)形式存在于泌乳乳腺的核提取物中,并与这个BLG控制元件中的至少5个位点结合。此外,一种对小鼠和绵羊泌乳乳腺提取物都特异的因子(乳蛋白结合因子,MPBF)与3个BLG启动子位点结合,可能是一种乳蛋白基因转录因子。