Bulfield G, Trent J
Biochem Genet. 1981 Feb;19(1-2):87-93. doi: 10.1007/BF00486139.
During a screening of inbred strains for enzyme variation in glycolysis, differences were found in glyceraldehyde phosphate dehydrogenase (GAPDH) activity between C57BL/6J and SM/J mice. Segregation analysis did not reveal unequivocal monogenic inheritance. Dialysis of hemolysates caused decay of enzyme activity, especially in C57BL animals, which could be prevented by the presence of NAD. This led to the finding that erythrocyte NAD levels were threefold higher in SM than C57BL animals and, although additively inherited, did not appear to be monogenic. This is comparable with but independent of the differences and effect of erythrocyte NADP levels on glucose-6 phosphate dehydrogenase activity reported by R. P. Erickson (1974) Biochem. Genet. 11:33] and emphasizes the range of mechanisms that can be involved in the genetic control of enzyme activity in mammalian systems.
在对近交系进行糖酵解酶变异筛查的过程中,发现C57BL/6J小鼠和SM/J小鼠之间的甘油醛磷酸脱氢酶(GAPDH)活性存在差异。分离分析未揭示明确的单基因遗传。溶血产物的透析导致酶活性衰减,尤其是在C57BL品系动物中,而NAD的存在可防止这种衰减。这一发现表明,SM品系动物红细胞中的NAD水平比C57BL品系动物高三倍,并且尽管呈加性遗传,但似乎并非单基因遗传。这与R.P.埃里克森(1974年,《生物化学遗传学》11:33)报道的红细胞NADP水平对葡萄糖-6-磷酸脱氢酶活性的差异及影响类似,但相互独立,强调了哺乳动物系统中酶活性遗传控制可能涉及的多种机制。