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Genetic analysis of alpha-fetoprotein synthesis in mice.

机译:小鼠甲胎蛋白合成的遗传分析。

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The differential induction of alpha-fetoprotein (AFP) mRNA during liver regeneration in three inbred strains of mice was examined to determine the genetic and molecular bases for the differences in protein production. BALB/cJ, C3H/He, and C57BL/6 mice, previously identified as high, intermediate, and low AFP producers, respectively, were used. Liver AFP mRNA concentrations during normal development and after carbon tetrachloride administration were measured and shown to correlate exactly with the serum protein concentrations. By performing a series of genetic crosses, we identified two unlinked genetic loci that acted independently to affect the inducibility of AFP mRNA. The raf gene, previously identified by Olsson et al. (J. Exp. Med. 145:819-827, 1977), determines the adult basal level of AFP mRNA, and the Rif gene affects its inducibility during regeneration. By using a polymorphic restriction endonuclease site within the albumin-AFP structural gene region, we show that neither regulatory gene is closely linked to the structural genes. In addition, neither gene affects the concentration of albumin mRNA during development or liver regeneration.
机译:检查了三个自交系小鼠肝脏再生过程中甲胎蛋白(AFP)mRNA的差异诱导,以确定蛋白质生产差异的遗传和分子基础。使用先前分别确定为高,中和低AFP生产者的BALB / cJ,C3H / He和C57BL / 6小鼠。测量了正常发育过程中和四氯化碳给药后的肝AFP mRNA浓度,显示与血清蛋白浓度精确相关。通过执行一系列的遗传杂交,我们确定了两个独立的基因位点,它们独立发挥作用来影响AFP mRNA的诱导性。 raf基因,先前由Olsson等人鉴定。 (J. Exp。Med。145:819-827,1977),确定成人AFP mRNA的基础水平,而Rif基因在再生过程中会影响其诱导性。通过使用白蛋白-AFP结构基因区域内的多态性限制性内切核酸酶位点,我们表明这两个调节基因都没有与结构基因紧密相连。此外,这两个基因均不会影响发育或肝脏再生过程中白蛋白mRNA的浓度。

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