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Haploinsufficiency and the sex chromosomes from yeasts to humans

机译:单倍剂量不足和从酵母到人类的性染色体

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Background Haploinsufficient (HI) genes are those for which a reduction in copy number in a diploid from two to one results in significantly reduced fitness. Haploinsufficiency is increasingly implicated in human disease, and so predicting this phenotype could provide insights into the genetic mechanisms behind many human diseases, including some cancers. Results In the present work we show that orthologues of Saccharomyces cerevisiae HI genes are preferentially retained across the kingdom Fungi, and that the HI genes of S. cerevisiae can be used to predict haploinsufficiency in humans. Our HI gene predictions confirm known associations between haploinsufficiency and genetic disease, and predict several further disorders in which the phenotype may be relevant. Haploinsufficiency is also clearly relevant to the gene-dosage imbalances inherent in eukaryotic sex-determination systems. In S. cerevisiae , HI genes are over-represented on chromosome III, the chromosome that determines yeast's mating type. This may be a device to select against the loss of one copy of chromosome III from a diploid. We found that orthologues of S. cerevisiae HI genes are also over-represented on the mating-type chromosomes of other yeasts and filamentous fungi. In animals with heterogametic sex determination, accumulation of HI genes on the sex chromosomes would compromise fitness in both sexes, given X chromosome inactivation in females. We found that orthologues of S. cerevisiae HI genes are significantly under-represented on the X chromosomes of mammals and of Caenorhabditis elegans . There is no X inactivation in Drosophila melanogaster (increased expression of X in the male is used instead) and, in this species, we found no depletion of orthologues to yeast HI genes on the sex chromosomes. Conclusion A special relationship between HI genes and the sex/mating-type chromosome extends from S. cerevisiae to Homo sapiens , with the microbe being a useful model for species throughout the evolutionary range. Furthermore, haploinsufficiency in yeast can predict the phenotype in higher organisms.
机译:背景单倍体不足(HI)基因是那些二倍体的拷贝数从2个减少到1个导致适应性显着降低的基因。单倍功能不足与人类疾病的关系日益密切,因此预测这种表型可以提供许多人类疾病(包括某些癌症)背后的遗传机制的见解。结果在目前的工作中,我们显示了酿酒酵母HI基因的直向同源物在真菌界中被优先保留,并且酿酒酵母的HI基因可用于预测人类的单倍体功能不足。我们的HI基因预测证实了单倍剂量不足与遗传疾病之间的已知关联,并预测了可能与表型有关的其他疾病。单倍剂量不足也与真核生物性别决定系统固有的基因剂量失衡有关。在酿酒酵母中,HI基因在染色体III(代表酵母交配类型的染色体)上过分代表。这可能是一种选择以防止二倍体丢失一个染色体III拷贝的设备。我们发现酿酒酵母HI基因的直向同源物在其他酵母和丝状真菌的交配型染色体上也被过度表达。在具有异配子性的动物中,鉴于雌性X染色体失活,性染色体上HI基因的积累会损害两性的适应性。我们发现,酿酒酵母HI基因的直向同源物在哺乳动物和秀丽隐杆线虫的X染色体上的表达明显不足。果蝇中没有X失活(取而代之的是使用男性中X的增加表达),在该物种中,我们没有发现直向同源物耗尽性染色体上的酵母HI基因。结论HI基因与性别/交配型染色体之间的特殊关系从啤酒酵母到智人,微生物是整个进化范围内物种的有用模型。此外,酵母中的单倍剂量不足可以预测高等生物中的表型。

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