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首页> 外文期刊>PLoS Genetics >The Rose-comb Mutation in Chickens Constitutes a Structural Rearrangement Causing Both Altered Comb Morphology and Defective Sperm Motility
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The Rose-comb Mutation in Chickens Constitutes a Structural Rearrangement Causing Both Altered Comb Morphology and Defective Sperm Motility

机译:鸡的玫瑰梳状突变构成结构重排,导致梳状形态改变和精子活动力降低

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摘要

Rose-comb, a classical monogenic trait of chickens, is characterized by a drastically altered comb morphology compared to the single-combed wild-type. Here we show that Rose-comb is caused by a 7.4 Mb inversion on chromosome 7 and that a second Rose-comb allele arose by unequal crossing over between a Rose-comb and wild-type chromosome. The comb phenotype is caused by the relocalization of the MNR2 homeodomain protein gene leading to transient ectopic expression of MNR2 during comb development. We also provide a molecular explanation for the first example of epistatic interaction reported by Bateson and Punnett 104 years ago, namely that walnut-comb is caused by the combined effects of the Rose-comb and Pea-comb alleles. Transient ectopic expression of MNR2 and SOX5 (causing the Pea-comb phenotype) occurs in the same population of mesenchymal cells and with at least partially overlapping expression in individual cells in the comb primordium. Rose-comb has pleiotropic effects, as homozygosity in males has been associated with poor sperm motility. We postulate that this is caused by the disruption of the CCDC108 gene located at one of the inversion breakpoints. CCDC108 is a poorly characterized protein, but it contains a MSP (major sperm protein) domain and is expressed in testis. The study illustrates several characteristic features of the genetic diversity present in domestic animals, including the evolution of alleles by two or more consecutive mutations and the fact that structural changes have contributed to fast phenotypic evolution.
机译:玫瑰梳是鸡的经典单基因特征,其特征是与单梳野生型相比,梳形态发生了巨大变化。在这里,我们显示玫瑰梳是由7号染色体上的7.4 Mb倒位引起的,并且第二个玫瑰梳等位基因是由玫瑰梳和野生型染色体之间的不相等交叉产生的。梳状表型是由MNR2同源域蛋白基因的重新定位引起的,从而导致在梳状发育过程中MNR2的瞬时异位表达。我们还为Bateson和Punnett 104年前报道的上位相互作用的第一个例子提供了分子解释,即核桃梳是由玫瑰梳和豌豆梳等位基因的共同作用引起的。 MNR2和SOX5的瞬时异位表达(导致豌豆梳表型)发生在同一间充质细胞群体中,并且在梳原基中的单个细胞中表达至少部分重叠。玫瑰梳具有多效性,因为男性的纯合性与精子活力差有关。我们假设这是由于CCDC108基因位于一个反转断点之一的破坏引起的。 CCDC108是一种表征较差的蛋白质,但它包含MSP(主要精子蛋白质)结构域,并在睾丸中表达。该研究说明了家畜中遗传多样性的几个特征,包括两个或多个连续突变引起的等位基因进化,以及结构变化促进了快速表型进化的事实。

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