Robinson J L, Drabik M R, Dombrowski D B, Clark J H
Proc Natl Acad Sci U S A. 1983 Jan;80(2):321-3. doi: 10.1073/pnas.80.2.321.
Several dairy cows have been identified as partially deficient in UMP synthase. Although erythrocytes of normal cows contained 2.54 units of enzyme per ml, four cows were discovered with only 1.08 units per ml. Cows deficient in UMP synthase secreted milk with abnormally high levels of orotate, 300-1,000 micrograms of orotate per ml compared to 80 micrograms/ml for normal cows. The deficiency also was accompanied by a lactation-induced orotic aciduria. Although bovine urinary orotate was generally less than 10 micrograms/ml, the urine of the deficient cows, when lactating, contained 20-200 micrograms/ml. Their plasma orotate also was elevated. Genetic transmission of the condition was suggested by a common bull in the pedigrees of all deficient animals. Indeed, these cows, with half the normal level of UMP synthase, are probably heterozygotes with a 50% chance of passing the deficient allele to their progeny. For these putative heterozygotes, the condition is apparently benign because longevity and production were unaffected. However, the existence of a gene for UMP synthase deficiency in the dairy cow population poses a hazard with respect to the conception of homozygotic, deficient animals. These, in analogy with a comparable human condition, would be expected to exhibit high perinatal morbidity and mortality.
已鉴定出几头奶牛存在尿苷一磷酸合酶部分缺陷。正常奶牛的红细胞每毫升含有2.54单位的该酶,而发现有四头奶牛每毫升仅含1.08单位。尿苷一磷酸合酶缺陷的奶牛分泌的乳汁中乳清酸水平异常高,每毫升含300 - 1000微克乳清酸,而正常奶牛每毫升为80微克。这种缺陷还伴有泌乳诱导的乳清酸尿症。虽然牛尿液中的乳清酸一般低于每毫升10微克,但缺陷奶牛在泌乳时,尿液中含有每毫升20 - 200微克。它们的血浆乳清酸也有所升高。所有缺陷动物的系谱中都有一头共同的公牛,这表明该病症存在遗传传递。实际上,这些奶牛的尿苷一磷酸合酶水平为正常水平的一半,可能是杂合子,有50%的机会将缺陷等位基因传给后代。对于这些假定的杂合子来说,这种情况显然是良性的,因为寿命和生产未受影响。然而,奶牛群体中存在尿苷一磷酸合酶缺陷基因对纯合缺陷动物的受孕构成了风险。与类似的人类疾病情况类似,预计这些纯合缺陷动物会表现出高围产期发病率和死亡率。