Bernstine E G, Koh C, Lovelace C C
Proc Natl Acad Sci U S A. 1979 Dec;76(12):6539-41. doi: 10.1073/pnas.76.12.6539.
In a previous study [Bernstine, E.G. (1979) J. Biol. Chem. 254, 83-87] it was shown that inbred strains of mice fall into two classes based on the specific activity of mitochondrial malic enzyme [L-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating), EC 1.1.1.40] in brain. In this report we demonstrate differences between high- and low-activity strains in the development of enzyme activity levels in adult mice and show that the rate of enzyme synthesis quantitatively accounts for the inherited level of the brain enzyme. Genetic analysis has established that the locus controlling the amount of enzyme in brain (Mdr-1) is located on chromosome 7. Its linkage to Hbb and c places it in the same region of the chromosome as Mod-2, the structural gene for mitochondrial malic enzyme. By making use of deletions and a duplication that include Mod-2, evidence for cis action of Mdr-1 was obtained.
在之前的一项研究中[伯恩斯坦,E.G.(1979年)《生物化学杂志》254卷,第83 - 87页]表明,根据小鼠脑中线粒体苹果酸酶[L - 苹果酸:NADP⁺氧化还原酶(草酰乙酸脱羧),EC 1.1.1.40]的比活性,近交系小鼠可分为两类。在本报告中,我们展示了高活性和低活性品系成年小鼠中酶活性水平发展的差异,并表明酶合成速率在数量上决定了脑酶的遗传水平。遗传分析已确定,控制脑中酶量的基因座(Mdr - 1)位于7号染色体上。它与Hbb和c的连锁关系将其定位在与线粒体苹果酸酶的结构基因Mod - 2相同的染色体区域。通过利用包含Mod - 2的缺失和重复,获得了Mdr - 1顺式作用的证据。