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The Drosophila Over Compensating Males Gene Genetically Inhibits Dosage Compensation in Males

机译:果蝇过度补偿男性基因遗传抑制男性剂量补偿。

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摘要

Male Drosophila are monosomic for the X chromosome, but survive due to dosage compensation. They use the Male Specific Lethal (MSL) complex composed of noncoding roX RNA and histone modifying enzymes to hypertranscribe most genes along the X ∼1.6–1.8 fold relative to each female allele. It is not known how the MSL complex achieves this precise adjustment to a large and diverse set of target genes. We carried out a genetic screen searching for novel factors that regulate dosage compensation in flies. This strategy generated thirty alleles in a previously uncharacterized gene, over compensating males (ocm) that antagonizes some aspect of MSL activity. The mutations were initially recovered because they derepressed an MSL-dependent eye color reporter. Null ocm mutations are lethal to both sexes early in development revealing an essential function. Combinations of hypomorphic ocm alleles display a male specific lethality similar to mutations in the classic msl genes, but ocm males die due to excessive, rather than lack of dosage compensation. Males that die due to very low MSL activity can be partially rescued by ocm mutations. Likewise, males that would die from ocm mutations can be rescued by reducing the dose of various msl and roX genes. ocm encodes a large nuclear protein that shares a novel cysteine rich motif with known transcription factors.
机译:雄性果蝇在X染色体上是单体的,但由于剂量补偿而存活。他们使用由非编码roX RNA和组蛋白修饰酶组成的雄性特异性致死(MSL)复合物,沿每个女性等位基因的X〜1.6-1.8倍超转录大多数基因。未知的是,MSL复合物如何实现对大量多样的靶基因的精确调节。我们进行了基因筛选,以寻找可调节果蝇剂量补偿的新因素。这种策略在先前无法鉴定的基因中产生了三十个等位基因,超过了补偿雄性(ocm)的能力,从而抵消了MSL活性的某些方面。这些突变最初被恢复,因为它们抑制了依赖MSL的眼睛颜色报告基因。无效的ocm突变在发育早期对男女都具有致命性,揭示了一种基本功能。亚型ocm等位基因的组合表现出类似于经典msl基因突变的男性特异性致死率,但ocm男性死于过量而不是缺乏剂量补偿。由于MSL活性极低而死亡的男性可以通过ocm突变部分挽救。同样,可以通过减少各种msl和roX基因的剂量来挽救因ocm突变而死亡的雄性。 ocm编码一种较大的核蛋白,该蛋白与已知的转录因子共享一个富含半胱氨酸的新颖基序。

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  • 总页数 10
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