Brem G, Brenig B, Salmons B, Wolf E, Müller M, Erfle V, Günzburg W H, Dahme E
Lehrstuhl für Molekulare Tierzucht am Institut für Tierzucht und Tierhygiene, Ludwig-Maximilians-Universität München.
Tierarztl Prax. 1991 Aug;19(4):345-50.
Pronuclear microinjection was used to produce transgenic mice harboring gene constructs, in which 110 base pairs (WAP1) or 2.4 kilobases (WAP2) of the 5' flanking sequences of the whey acidic protein (WAP) gene were fused to human growth hormone (hGH)-coding sequences. Female WAP-hGH transgenic mice expressed the transgenes in the mammary gland, the expression of the WAP2-hGH transgene mirroring that of the endogenous WAP gene. When other organs were examined, high level expression of hGH was observed in the brains of WAP2-hGH transgenic mice. Using in situ hybridization and immunohistochemistry, hGH expression from the transgene was seen to occur specifically in Bergmann glia cells. While normally neither WAP nor hGH is expressed in this type of cell, it appears that a combination of the regulatory region of the WAP gene and the hGH structural gene results in a novel tissue specificity in Bergmann glia cells.
采用原核显微注射法制备携带基因构建体的转基因小鼠,其中乳清酸性蛋白(WAP)基因5'侧翼序列的110个碱基对(WAP1)或2.4千碱基(WAP2)与人生长激素(hGH)编码序列融合。雌性WAP-hGH转基因小鼠在乳腺中表达转基因,WAP2-hGH转基因的表达反映了内源性WAP基因的表达。当检查其他器官时,在WAP2-hGH转基因小鼠的大脑中观察到hGH的高水平表达。通过原位杂交和免疫组织化学方法,发现转基因的hGH表达特异性地发生在伯格曼胶质细胞中。虽然正常情况下WAP和hGH在这类细胞中均不表达,但似乎WAP基因的调控区域和hGH结构基因的组合导致了伯格曼胶质细胞中一种新的组织特异性。