%0 Journal Article %T 水牛<i>STAT</i>5<i>a</i>和<i>STAT</i>5<i>b</i>基因启动子克隆及其活性分析<br>Cloning and Activity Analysis of Buffalo <i>STAT</i>5<i>a</i> and <i>STAT</i>5<i>b</i> Promoters %A 李胜 %A 黄时海 %A 张艳 %A 石德顺 %A 李湘萍< %A br> %A LI Sheng %A HUANG Shi-hai %A ZHANG Yan %A SHI De-shun %A LI Xiang-ping %J 西南大学学报(自然科学版) %D 2018 %R 10.13718/j.cnki.xdzk.2018.01.001 %X 为了解转录激活与信号转导因子5(STAT5)在水牛乳腺发育及泌乳生理中的功能，对水牛<i>STAT</i>5<i>a</i>和<i>STAT</i>5<i>b</i>基因的5′调控区启动子序列进行了克隆，并比较其活性.根据GenBank已公布的牛<i>STAT</i>5<i>a</i>和<i>STAT</i>5<i>b</i>基因序列设计特异性引物，以广西本地水牛乳腺组织基因组DNA为模板，通过PCR法分别扩增不同长度<i>STAT</i>5<i>a</i>和<i>STAT</i>5<i>b</i>基因启动子片段并进行生物信息学分析.结果表明：克隆得到的水牛<i>STAT</i>5<i>a</i>基因启动子片段(P1和P2)大小是500 bp，700 bp，<i>STAT</i>5<i>b</i>基因启动子片段(P3，P4和P5)大小是500 bp，800 bp，1 500 bp.在线分析结果显示，仅P2片段中存在高甲基化位点，且富含SP1，AP2等转录因子结合位点.将构建的不同长度启动子片段分别连入pGL3-Basic载体，分别转染水牛乳腺上皮细胞，检测荧光素酶表达水平.与未转染组相比，P1~P5质粒转染组的荧光素酶比值均显著提高(<i>p</i>＜0.05)；添加5 mg/mL质量浓度催乳素(PRL)处理乳腺上皮细胞，P3质粒转染组的荧光素酶比值显著高于其他各组(<i>p</i>＜0.05).以上结果表明，水牛<i>STAT</i>5<i>a</i>和<i>STAT</i>5<i>b</i>基因启动子活性均受到PRL调节，两者表达水平在水牛乳腺上皮细胞中不同，且<i>STAT</i>5<i>b</i>基因表达受PRL调控更为明显.<br>In order to understand the role of transcriptional activation and signal transduction factor 5 (STAT5) protein in the development of the mammary gland and lactation in buffalo, we cloned and analyzed the promoter sequences of 5'regulatory region of <i>STAT</i>5<i>a</i> and <i>STAT</i>5<i>b</i> genes and compared their activity. We designed specific primers according to the <i>STAT</i>5<i>a</i> and <i>STAT</i>5<i>b</i> gene sequences published in GenBank, used the mammary gland tissue genomic DNA of Guangxi local buffaloes as a template, amplified the promoter fragments of <i>STAT</i>5<i>a</i> and <i>STAT</i>5<i>b</i> genes by PCR, and made bioinformatics analysis of them. The size of the promoter fragments (P1 and P2) of the buffalo <i>STAT</i>5<i>a</i> gene was shown to be 500 bp and 700 bp, and the size of the promoter fragments (P3, P4 and P5) of the <i>STAT</i>5<i>b</i> gene was 500 bp, 800 bp and 1500 bp, respectively. The results of on-line analysis showed that there were hypermethylation sites in P2 fragment, which were also rich in transcription factor binding sites such as SP1 and AP2. The promoter fragments were inserted into pGL3-Basic vector, and transfected into buffalo mammary epithelial cells respectively. Detection of the expression level of luciferase showed that the ratio of luciferase in P1~P5 plasmid transfected group was significantly %K 水牛 %K < %K i> %K STAT< %K /i> %K 5< %K i> %K a< %K /i> %K < %K i> %K STAT< %K /i> %K 5< %K i> %K b< %K /i> %K 启动子 %K PRL %K 活性< %K br> %K buffalo %K < %K i> %K STAT< %K /i> %K 5< %K i> %K a< %K /i> %K < %K i> %K STAT< %K /i> %K 5< %K i> %K b< %K /i> %K promoter %K PRL (prolactin) %K activity %U http://xbgjxt.swu.edu.cn/jsuns/html/jsuns/2018/1/201801001.htm