Mouse models of aneuploidy to understand chromosome disorders.

Justin Tosh, Victor Tybulewicz, Elizabeth M C Fisher
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Abstract

An organism or cell carrying a number of chromosomes that is not a multiple of the haploid count is in a state of aneuploidy. This condition results in significant changes in the level of expression of genes that are gained or lost from the aneuploid chromosome(s) and most cases in humans are not compatible with life. However, a few aneuploidies can lead to live births, typically associated with deleterious phenotypes. We do not understand why phenotypes arise from aneuploid syndromes in humans. Animal models have the potential to provide great insight, but less than a handful of mouse models of aneuploidy have been made, and no ideal system exists in which to study the effects of aneuploidy per se versus those of raised gene dosage. Here, we give an overview of human aneuploid syndromes, the effects on physiology of having an altered number of chromosomes and we present the currently available mouse models of aneuploidy, focusing on models of trisomy 21 (which causes Down syndrome) because this is the most common, and therefore, the most studied autosomal aneuploidy. Finally, we discuss the potential role of carrying an extra chromosome on aneuploid phenotypes, independent of changes in gene dosage, and methods by which this could be investigated further.

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小鼠非整倍体模型了解染色体疾病。
携带非单倍体数倍染色体的生物体或细胞处于非整倍体状态。这种情况导致从非整倍体染色体获得或丢失的基因表达水平发生显著变化,并且大多数人类病例与生命不相容。然而,少数非整倍体可以导致活产,通常与有害表型相关。我们不明白为什么人类的非整倍体综合征会产生表型。动物模型有可能提供很好的见解,但已经建立的非整倍性小鼠模型屈指可数,并且不存在理想的系统来研究非整倍性本身与增加基因剂量的影响。在这里,我们概述了人类非整倍体综合征,染色体数量改变对生理的影响,并介绍了目前可用的小鼠非整倍体模型,重点关注21三体模型(导致唐氏综合症),因为这是最常见的,因此也是研究最多的常染色体非整倍体。最后,我们讨论了携带额外染色体对非整倍体表型的潜在作用,独立于基因剂量的变化,以及可以进一步研究的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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