Latter M R, Latter B D H, Wilkins J F, Windsor P A
NSW Agriculture, Agricultural Research and Advisory Station, Grafton, New South Wales.
Aust Vet J. 2006 Apr;84(4):122-8. doi: 10.1111/j.1751-0813.2006.tb13394.x.
To determine the mode of inheritance of congenital proportionate dwarfism in Angus and Angus crossbred cattle, initially detected in two commercial beef herds in northern New South Wales.
Matings of normal carrier sires to unrelated cows of diverse breeds, and of one carrier sire to his unaffected daughters. An unrelated Piedmontese bull was also mated to unaffected daughters of the carrier sires.
Two carrier Angus bulls and nine unaffected daughters, all of whom were completely indistinguishable from normal animals, were purchased for controlled breeding studies under known nutritional and disease conditions. Affected and carrier individuals were examined for the presence of obvious chromosomal abnormalities.
Angus dwarfism has been successfully reproduced under controlled experimental conditions over successive years using unrelated dams and is undoubtedly heritable. The high frequency of occurrence of affected individuals (23/61 = 0.38 +/- .06) among the progeny of matings of the Angus sires to unrelated females of diverse breeding is not compatible with recessive inheritance, because of the negligible frequency of proportionate dwarfism in the breeds of the dams. Both paternal and maternal transmission of the defect was demonstrated, so that imprinting in the strict sense of a gene that is only expressed when received from the male parent appears not to be involved. Tested individuals showed no evidence of gross chromosomal abnormality. Dominant autosomal inheritance with incomplete penetrance was indicated by the lack of expression of the defective gene in the two Angus sires and in three unaffected daughters who produced dwarf calves from matings to the Piedmontese bull.
The mode of inheritance is that of a single autosomal dominant gene with a penetrance coefficient of 0.75 +/- 0.12, estimated from the observed incidence of 23/61 affected offspring of the two carrier Angus bulls mated to unrelated dams. Simple genetic models involving either (i) an unstable mutant which changes at high frequency to the expressed dominant dwarfing allele during gametogenesis, or (ii) a dominant allele with penetrance determined by an unlinked modifying locus, are shown to be compatible with the experimental data. Both models indicate that penetrance of the dwarfing gene may possibly be higher in matings involving carrier daughters of the two Angus bulls.
确定最初在新南威尔士州北部两个商业肉牛群中发现的安格斯及安格斯杂交牛先天性匀称性侏儒症的遗传模式。
正常携带基因的公牛与不同品种的无亲缘关系母牛进行交配,以及一头携带基因的公牛与其未受影响的女儿进行交配。一头无亲缘关系的皮埃蒙特公牛也与携带基因公牛的未受影响女儿进行交配。
购买了两头携带基因的安格斯公牛和九头未受影响的女儿,所有这些牛与正常动物完全无法区分,用于在已知营养和疾病条件下进行的控制性繁殖研究。对受影响和携带基因的个体进行检查,看是否存在明显的染色体异常。
多年来,利用无亲缘关系的母本在控制性实验条件下成功繁殖出安格斯侏儒症,无疑具有遗传性。安格斯公牛与不同品种的无亲缘关系雌性交配产生的后代中,受影响个体的出现频率较高(23/61 = 0.38 ± 0.06),这与隐性遗传不相符,因为母本品种中匀称性侏儒症的发生频率可忽略不计。已证明缺陷可通过父系和母系传递,因此严格意义上仅在从父本遗传时才表达的基因印记似乎不涉及其中。受试个体未显示出明显染色体异常的证据。两个安格斯公牛以及三头未受影响的女儿(它们与皮埃蒙特公牛交配后产下侏儒小牛)中缺陷基因未表达,这表明存在具有不完全外显率的显性常染色体遗传。
遗传模式为单个常染色体显性基因,外显率系数为0.75 ± 0.12,这是根据两头携带基因的安格斯公牛与无亲缘关系母本交配产生的23/61受影响后代的观察发病率估算得出的。涉及以下两种情况的简单遗传模型:(i)一个不稳定的突变体,在配子发生过程中高频突变为表达的显性侏儒等位基因;或(ii)一个显性等位基因,其外显率由一个不连锁的修饰基因座决定,均与实验数据相符。两种模型均表明,在涉及两头安格斯公牛携带基因女儿的交配中,侏儒基因的外显率可能更高。