Gutiérrez A, Meade H M, Ditullio P, Pollock D, Harvey M, Jiménez-Flores R, Anderson G B, Murray J D, Medrano J F
Department of Animal Science, University of California, Davis 95616-8521, USA.
Transgenic Res. 1996 Jul;5(4):271-9. doi: 10.1007/BF01972881.
Transgenic mice were produced by microinjection of a DNA construct composed of the bovine kappa-casein (kappa-CN) cDNA under the control of the goat beta-CN 5' promoter elements and 3' flanking regions into pronuclear-stage embryos. The gene construct targeted the expression of bovine kappa-CN RNA to the mammary gland and secretion of bovine kappa-CN in the milk. In the three lines studied (BC-7, BC-31 and BC-67) the transgene was stably integrated and propagated as a Mendelian locus. Expression of the bovine protein in lactating mice from the three transgenic lines was demonstrated by northern and western blots. In ten different tissues analysed by northern blotting, expression was confined to the mammary gland of lactating transgenic mice from line BC-7, with low-level expression also observed in the salivary gland of lines BC-31 and BC-67. Transgene expression in the mammary gland paralleled normal casein gene expression during lactation and was not observed in virgin females. The level of bovine kappa-CN mRNA expression on day 10 of lactation in hemizygous transgenic females in relation to endogenous mRNA of whey acid protein (WAP) gene expression was 14%, 69%, and 127% in lines BC-7, BC-31 and BC-67, respectively. No association between transgene copy number and expression was observed. The bovine kappa-CN concentration in milk on day 10 of lactation ranged from 0.94 to 3.85 mg of protein per ml of milk. The bovine kappa-CN expressed in mouse milk had the same molecular mass and immunoactivity with polyclonal antibodies as did kappa-CN from bovine milk. A high degree of variation in the production of bovine kappa-CN within each of the transgenic lines was observed.
通过将由山羊β-酪蛋白5'启动子元件和3'侧翼区域控制的牛κ-酪蛋白(κ-CN)cDNA组成的DNA构建体显微注射到原核期胚胎中,产生了转基因小鼠。该基因构建体将牛κ-CN RNA的表达靶向乳腺,并使牛κ-CN分泌到乳汁中。在所研究的三个品系(BC-7、BC-31和BC-67)中,转基因作为孟德尔位点稳定整合并遗传。通过Northern印迹和Western印迹证实了三个转基因品系的泌乳小鼠中牛蛋白的表达。在通过Northern印迹分析的十种不同组织中,表达仅限于BC-7品系泌乳转基因小鼠的乳腺,在BC-31和BC-67品系的唾液腺中也观察到低水平表达。乳腺中的转基因表达与泌乳期间正常酪蛋白基因表达平行,在未生育的雌性小鼠中未观察到。在半合子转基因雌性小鼠泌乳第10天,相对于乳清酸性蛋白(WAP)基因表达的内源性mRNA,牛κ-CN mRNA表达水平在BC-7、BC-31和BC-67品系中分别为14%、69%和127%。未观察到转基因拷贝数与表达之间的关联。泌乳第10天牛奶中牛κ-CN的浓度范围为每毫升牛奶0.94至3.85毫克蛋白质。小鼠乳汁中表达的牛κ-CN与来自牛奶的κ-CN具有相同的分子量和与多克隆抗体的免疫活性。在每个转基因品系中观察到牛κ-CN产量的高度差异。