大鼠OSP-1启动子克隆与表达检测

[目的]克隆大鼠卵巢特异性启动子(OSP-1)片段,并在细胞水平检测该启动子调控标记基因的组织特异性表达。[方法]参考已知大鼠OSP-1序列设计特异性引物,PCR扩增大鼠OSP-1启动子片段并与已公布的大鼠OSP-1序列进行比较。将OSP-1启动子定向克隆到去除CMV的pEGFP-N1载体,构建真核表达载体pOSP-1-EGFP-N1;重组质粒在脂质体LipofectamineTM2000介导下,分别转染水牛的颗粒细胞、乳腺上皮细胞和胎儿成纤维细胞,并于转染后12,24和48h在荧光显微镜下观察EGFP表达情况。[结果]OSP-1启动子扩增片段长480bp,与已公布的大鼠OSP-1序列的相似性达96%;应用启动子预测软件对所得序列分析表明,该扩增片段含有类似于TA-TAbox和CAATbox的核心启动顺式元件,并含有多个C/EBPbeta转录因子的结合位点;在颗粒细胞转染后12h可观测到绿色荧光表达,转染后24h荧光细胞增多,细胞形态均呈圆形、体积较大,48h荧光细胞数量骤减,且死细胞增多;在乳腺上皮细胞和胎儿成纤维细胞均未检测到EGFP基因表达。[结论]大鼠OSP-1启动子控制下的EGFP基因可在水牛颗粒细胞中特异表达,为构建水牛卵巢特异性表达转基因载体奠定了基础。

Algebraic Bethe Ansatz for the Osp(1|2) Model with Reflecting Boundaries

In the framework of graded quantum inverse scattering method, we obtain the eigenvalues and the eigenvectors of the Osp(l|2) model with reflecting boundary conditions in FBF background. The corresponding Bathe ansatz equations are obtained.

THE SUPER-BIHAMILTONIAN REDUCTION ON C~∞(S^1, OSP(1|2))

In this article, we will show that the super-bihamiltonian structures of the Kuper- KdV equation in [3], the Kuper-CH equation in [17, 18] and the super-HS equation in [11, 16, 19] can be obtained by applying a super-bihamiltonian reduction of different super-Poisson pairs defined on the loop algebra of osp（1｜2）.

OSP-1启动子在奶山羊卵巢颗粒细胞中的转录活性

采用大鼠OSP-1启动子替换掉pcDNA3.1(+)中的CMV启动子,在其下游插入EGFP基因片段,构建载体pOSP-1-EGFP,脂质体转染不同细胞,利用荧光检测、RT-PCR以及相对定量PCR鉴定该启动子启动基因表达的活性。结果表明,在卵巢颗粒细胞、人卵巢癌细胞系HO-8910中可看到有绿色荧光;OSP-1片段只在卵巢颗粒细胞和人卵巢癌细胞系HO-8910有表达,并在人卵巢癌细胞系HO-8910中表达量较高,但是两者之间差异不显著。说明OSP-1启动子可调控外源基因在奶山羊卵巢颗粒细胞中特异性的表达。

9J COEFFICIENTS OF THE LIE SUPERALGEBRA OSP(1,2)

For the Lie superalgebra OSP(1, 2), we have studied the couplings of two and three irreducible representations, and calculated and discussed the corresponding coupling coefficients, especially Racah coefficients.