Zeindl-Eberhart E, Grohé G, Klose J
Institut für Humangenetik, Freie Universität Berlin, Federal Republic of Germany.
Hum Genet. 1987 Dec;77(4):371-8. doi: 10.1007/BF00291429.
Proteins were extracted from liver, brain, and skin of 6-day-old mice with trisomy (Ts) 19 and fractionated into solubilized cell proteins and structure-bound cell proteins. The proteins were separated by two-dimensional electrophoresis, and protein patterns were compared in the combinations Ts/normal and normal/normal. Analysis of the protein patterns revealed protein spots (variants) with densities higher (h-type) or lower (l-type) in trisomies than in normal mice. Some of these variants were found in all Ts individuals investigated for a particular protein class. These variants, termed regular Ts-variants, constituted 0.8%-1.6% of the total number of spots. The proteins of the regular Ts variants were in most cases organ-nonspecific. However, in almost all cases a given quantitative variation was expressed in only one of the three organs investigated. To explain our results, we have presented models for the control of protein levels on the basis of gene regulation. New aspects in the conception of studies on trisomies in man could be gained.
从19号三体(Ts)6日龄小鼠的肝脏、大脑和皮肤中提取蛋白质,并将其分离为可溶性细胞蛋白和结构结合细胞蛋白。通过二维电泳分离蛋白质,并比较Ts/正常和正常/正常组合中的蛋白质图谱。蛋白质图谱分析显示,三体小鼠中密度高于(h型)或低于(l型)正常小鼠的蛋白质斑点(变体)。在针对特定蛋白质类别研究的所有Ts个体中都发现了其中一些变体。这些变体被称为常规Ts变体,占斑点总数的0.8%-1.6%。常规Ts变体的蛋白质在大多数情况下是非器官特异性的。然而,几乎在所有情况下,给定的定量变化仅在三个研究器官中的一个中表达。为了解释我们的结果,我们基于基因调控提出了蛋白质水平控制模型。可以获得关于人类三体研究概念的新观点。