Andresen E
Anim Blood Groups Biochem Genet. 1977;8(3):149-56. doi: 10.1111/j.1365-2052.1977.tb01639.x.
Congenital nonspherocytic haemolytic anaemia (HA) in dogs of the Basenji breed is inherited as a simple, autosomal recessive trait. Previous results of pyruvate kinase (PK) assays suggest a causal relationship between the anaemia and PK deficiency in erythrocytes. In the present investigation assays of this enzyme have been performed on haemolysates from 45 Basenji dogs, comprising 3 anaemic and 42 non-anaemic individuals of which 13 were known heterozygotes. The PK activity in haemolysates from the 42 non-anaemic dogs exhibited a bimodal distribution corresponding to the genotypic classes: heterozygotes and normal homozygotes. The results indicate that heterozygotes have a partial, detectable enzyme deficiency, not reflected in clinical disease, and thus give evidence of a gene dosage effect in agreement with observations in man. The proposed genotypes PK PK, PK pk and pk pk refer to normal homozygotes, heterozygotes, and anaemic individuals, respectively. The findings strengthen the genetic hypothesis of recessiveness of the anaemia by direct detection of heterozygosity of parents of affected individuals. Moreover, the results are of value in comparative studies and they have practical application in connection with eradication programmes.
巴辛吉犬种的先天性非球形细胞溶血性贫血(HA)作为一种简单的常染色体隐性性状遗传。先前丙酮酸激酶(PK)检测结果表明贫血与红细胞中PK缺乏之间存在因果关系。在本研究中,对45只巴辛吉犬的溶血产物进行了该酶的检测,其中包括3只贫血犬和42只非贫血犬,后者中有13只是已知的杂合子。42只非贫血犬溶血产物中的PK活性呈现出对应于基因型类别的双峰分布:杂合子和正常纯合子。结果表明,杂合子有部分可检测到的酶缺乏,但未在临床疾病中体现,从而为与人类观察结果一致的基因剂量效应提供了证据。提议的基因型PK PK、PK pk和pk pk分别指正常纯合子、杂合子和贫血个体。这些发现通过直接检测患病个体父母的杂合性,强化了贫血隐性遗传的基因假说。此外,这些结果在比较研究中有价值,并且在根除计划方面有实际应用。