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可卡犬的遗传性XX性反转

Inherited XX sex reversal in the cocker spaniel dog.

作者信息

Selden J R, Moorhead P S, Koo G C, Wachtel S S, Haskins M E, Patterson D F

出版信息

Hum Genet. 1984;67(1):62-9. doi: 10.1007/BF00270560.

Abstract

Nine XX true hermaphrodites and two XX males were discovered in a family of American cocker spaniels. The true hermaphrodites were partially-masculinized females with ovotestes; the XX males had malformed male external genitalia and cryptorchid aspermatogenic testes. Wolffian and Mullerian duct derivatives were present in both true hermaphrodites and XX males. All four sires of sex-reversed dogs were normal XY males; five of the dams were anatomically normal females and one was an XX true hermaphrodite. A second true hermaphrodite reproduced as a female, producing anatomically normal offspring. All matings that produced sex-reversed offspring were consanguineous. Matings of the parents of sex-reversed cocker spaniels to normal beagles with no family history of intersexuality produced only normal offspring. Examination of G-banded karyotypes of the affected animals, their parents, and siblings, revealed no structural anomalies of the chromosomes that were consistently associated with sex-reversal. In assays for serologically-detectable H-Y antigen, the group of XX true hermaphrodites and the group of XX males had mean levels of the antigen not significantly different from that in normal male controls. Female parents of sex-reversed dogs and some of their female siblings were typed H-Y antigen positive, but the mean level of the antigen in this group was less than that of normal male controls. It is proposed that XX sex reversal in cocker spaniels is due to a mutant gene which when homozygous in females, results in a level of H-Y antigen similar to that found in normal males and the gonads develop as ovotestes or testes. When the gene is heterozygous in females, the level of serologically-detectable H-Y antigen is lower than that found in normal males and the gonads develop as normal ovaries. The persistence of Mullerian structures in the presence of testicular tissue suggests that Mullerian inhibiting substance is deficient or ineffective in its action in this condition.

摘要

在美国可卡犬的一个家族中发现了9只XX真两性畸形犬和2只XX雄性犬。真两性畸形犬是具有卵睾的部分男性化雌性;XX雄性犬有畸形的雄性外生殖器和隐睾无精子生成的睾丸。真两性畸形犬和XX雄性犬都有中肾管和副中肾管衍生物。所有性别反转犬的4只父犬都是正常的XY雄性;5只母犬在解剖学上是正常雌性,1只是XX真两性畸形犬。另一只真两性畸形犬以雌性身份繁殖,产下了解剖学上正常的后代。所有产生性别反转后代的交配都是近亲繁殖。将性别反转可卡犬的父母与无两性畸形家族史的正常比格犬交配,只产生了正常后代。对受影响动物及其父母和兄弟姐妹的G带核型进行检查,未发现与性别反转始终相关的染色体结构异常。在血清学可检测的H-Y抗原检测中,XX真两性畸形犬组和XX雄性犬组的抗原平均水平与正常雄性对照组无显著差异。性别反转犬的雌性父母及其一些雌性兄弟姐妹被检测为H-Y抗原阳性,但该组抗原的平均水平低于正常雄性对照组。有人提出,可卡犬的XX性别反转是由于一个突变基因,该基因在雌性中纯合时,会导致H-Y抗原水平与正常雄性相似,性腺发育为卵睾或睾丸。当该基因在雌性中杂合时,血清学可检测的H-Y抗原水平低于正常雄性,性腺发育为正常卵巢。在存在睾丸组织时副中肾管结构的持续存在表明,在此情况下副中肾管抑制物质缺乏或作用无效。

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