Kung M H, Lee Y J, Hsu J T, Huang M C, Ju Y T
Department of Animal Science and Technology, National Taiwan University, Taipei 10673, Taiwan.
Institute of Microbiology and Immunology, Chung Shan Medical University, Taichung 40201, Taiwan.
J Dairy Sci. 2015 Jun;98(6):3859-75. doi: 10.3168/jds.2014-9054. Epub 2015 Apr 1.
Goat β-casein (CSN2) promoter has been extensively used to derive expression of recombinant therapeutic protein in transgenic goats; however, little direct evidence exists for signaling molecules and the cis-elements of goat CSN2 promoter in response to lactogenic hormone stimulation in goat mammary epithelial cells. Here, we use an immortalized caprine mammary epithelial cell line (CMC) to search for evidence of the above. Serial 5'-flanking regions deleted of promoter and intron 1 in goat CSN2 (-4,047 to +2,054) driven by firefly luciferase reporter gene were constructed and applied to measure promoter activity in CMC. The intron 1 region (+393 to +501) significantly decreased basal activity of the promoter. This finding contradicts other studies of the role of intron 1. The signal transducer and activator of transcription (STAT)5a played a significant role in activating promoter activity by prolactin stimulation. Hydrocortisone enhanced and prolonged the activity of STAT5a and promoter in CMC, but was independent of the glucocorticoid receptor response element. The minimum length of the CSN2 promoter segment in response to lactogenic stimulation was confirmed by 5' serial deletions. A cis-element located from -300 to -90 in proximal goat CSN2 promoter that is absent in bovine and human CSN2 promoter was newly identified. We demonstrated the presence of a STAT5a binding site (-102 to -82) and preservation of the guanosine nucleotide at position -90 based on responses to the presence of lactogenic hormone using internal deletions and point mutations of the predicted STAT5a binding site, and chromatin immunoprecipitation assay. Together, these findings demonstrate that the proximal -300 bp of goat CSN2 promoter containing the STAT5a binding site (-102 to -82) is the response element for lactogenic hormone stimulation. Additionally, intron 1 may be required for tissue or developmental stage-specific expression in mammary gland. The role of the far-distal regions of goat CSN2 promoter in high-level lactogenic hormone induction and specific expression require further examination.
山羊β-酪蛋白(CSN2)启动子已被广泛用于在转基因山羊中驱动重组治疗性蛋白的表达;然而,关于山羊乳腺上皮细胞中响应催乳激素刺激的信号分子和山羊CSN2启动子的顺式元件,几乎没有直接证据。在此,我们使用永生化的山羊乳腺上皮细胞系(CMC)来寻找上述证据。构建了由萤火虫荧光素酶报告基因驱动的山羊CSN2(-4,047至+2,054)中启动子和内含子1的5'侧翼区域连续缺失的序列,并应用于测量CMC中的启动子活性。内含子1区域(+393至+501)显著降低了启动子的基础活性。这一发现与其他关于内含子1作用的研究相矛盾。信号转导和转录激活因子(STAT)5a在催乳素刺激激活启动子活性中起重要作用。氢化可的松增强并延长了CMC中STAT5a和启动子的活性,但与糖皮质激素受体反应元件无关。通过5'连续缺失证实了响应催乳激素刺激的CSN2启动子片段的最小长度。新鉴定了山羊CSN2近端启动子中位于-300至-90的一个顺式元件,该元件在牛和人CSN2启动子中不存在。基于对预测的STAT5a结合位点的内部缺失和点突变以及染色质免疫沉淀分析对催乳激素存在的反应,我们证明了STAT5a结合位点(-102至-82)的存在以及-90位鸟苷核苷酸的保留。总之,这些发现表明,包含STAT5a结合位点(-102至-82)的山羊CSN2启动子近端-300 bp是催乳激素刺激的反应元件。此外,内含子1可能是乳腺组织或发育阶段特异性表达所必需的。山羊CSN2启动子远端区域在高水平催乳激素诱导和特异性表达中的作用需要进一步研究。