Rijnkels M, Kooiman P M, Krimpenfort P J, de Boer H A, Pieper F R
Medical Biotechnology Department, Leiden Institute of Chemistry, Leiden University, The Netherlands.
Biochem J. 1995 Nov 1;311 ( Pt 3)(Pt 3):929-37. doi: 10.1042/bj3110929.
To identify cis-acting regulatory elements involved in the regulation of expression of the casein genes, the bovine beta-, alpha s2- and kappa-casein genes were isolated from cosmid libraries and introduced into the murine germline. Bovine casein expression was analysed at the RNA and protein level. The bovine beta-casein gene, including 16 kb of 5'- and 8 kb of 3'-flanking region, appeared to be expressed in all 12 transgenic mouse lines analysed. In 50% of these lines expression levels in milk exceeded 1 mg/ml. Three lines displayed expression levels comparable with or well above (20 mg/ml) the beta-casein levels in bovine milk. Transgene expression was restricted to the mammary gland. Strong induction of expression occurred at parturition and thus resembled the bovine rather than the murine pattern. In spite of this high-level tissue-specific and developmentally regulated expression, beta-casein expression levels were integration-site-dependent, suggesting that not all elements involved in regulation of expression were included in this beta-casein clone. Neither the bovine alpha s2- nor the kappa-casein gene, including 8 kb and 5 kb of 5'- and 1.5 kb and 19 kb of 3'-flanking sequences respectively, were properly expressed in transgenic mice. However, they were transcribed in stably transfected mouse mammary epithelial cells. This indicates that regulatory elements required for high-level, mammary gland-specific expression are not present in the alpha s2- and kappa-casein clones used in this study and are probably located elsewhere in the casein gene locus.
为了鉴定参与酪蛋白基因表达调控的顺式作用调控元件,从黏粒文库中分离出牛β-、αs2-和κ-酪蛋白基因,并将其导入小鼠种系。在RNA和蛋白质水平上分析了牛酪蛋白的表达。包含16 kb的5'侧翼区和8 kb的3'侧翼区的牛β-酪蛋白基因,在分析的所有12个转基因小鼠品系中似乎都有表达。在其中50%的品系中,乳汁中的表达水平超过1 mg/ml。三个品系的表达水平与牛乳中的β-酪蛋白水平相当或远高于(20 mg/ml)。转基因表达仅限于乳腺。在分娩时出现了强烈的表达诱导,因此类似于牛而不是小鼠的模式。尽管有这种高水平的组织特异性和发育调控表达,但β-酪蛋白的表达水平仍依赖于整合位点,这表明参与表达调控并非所有元件都包含在这个β-酪蛋白克隆中。包含分别8 kb和5 kb的5'侧翼序列以及1.5 kb和19 kb的3'侧翼序列的牛αs2-和κ-酪蛋白基因,在转基因小鼠中均未正确表达。然而,它们在稳定转染的小鼠乳腺上皮细胞中被转录。这表明在本研究中使用的αs2-和κ-酪蛋白克隆中不存在高水平乳腺特异性表达所需的调控元件,这些元件可能位于酪蛋白基因座的其他位置。