Berger F G, Paigen K
Nature. 1979 Nov 15;282(5736):314-6. doi: 10.1038/282314a0.
Several higher organisms have been reported in which enzyme levels are determined genetically by sites located in close proximity to the corresponding structural genes. In several cases, these sites have been shown to act by controlling the rates of enzyme synthesis. Cis compared with trans action has been tested for those proximate regulatory sites controlling enzymes for which appropriate structural variants exist. The rate of synthesis of beta-galactosidase in mouse tissues is under the control of a regulatory locus; Bgl-s, that is tightly linked to the enzyme structural gene; we have tested the cis/trans nature of Bgl-s action by analysis of the electrophoretic mobility of the enzyme from animals heterozygous for the appropriate regulatory and structural alleles. Our results indicate that Bgl-s acts cis, controlling the expression of the structural gene located on the same chromosome.
据报道,几种高等生物中,酶水平由位于相应结构基因附近的位点通过遗传方式决定。在一些情况下,这些位点已被证明通过控制酶的合成速率来发挥作用。对于那些控制具有适当结构变体的酶的近端调控位点,已测试了顺式作用与反式作用。小鼠组织中β-半乳糖苷酶的合成速率受一个调控基因座Bgl-s的控制,该基因座与酶结构基因紧密连锁;我们通过分析来自具有适当调控和结构等位基因杂合子动物的酶的电泳迁移率,测试了Bgl-s作用的顺式/反式性质。我们的结果表明,Bgl-s以顺式方式起作用,控制位于同一条染色体上的结构基因的表达。