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基因剂量敏感性与人类遗传疾病

Gene Dosage Sensitivity and Human Genetic Diseases.

作者信息

Veitia Reiner A, Zschocke Johannes, Birchler James A

机构信息

Université de Paris Cité, Paris, France.

Université de Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

出版信息

J Inherit Metab Dis. 2025 Jul;48(4):e70058. doi: 10.1002/jimd.70058.

Abstract

Here we review the historical background and contemporary insights into genetic dominance, focusing on haploinsufficiency (HI), that is, when the function of only one allele of a gene is not enough to ensure a normal phenotype in a diploid organism. A related phenomenon is triplosensitivity, that is, pathogenic effects when there are three instead of two copies of some 'genes'. The importance of gene dosage issues was realized in humans when whole chromosomal abnormalities (aneuploidy) could be linked to clinical phenotypes such as Down, Edwards, and Patau syndromes. Subsequently, subtler chromosomal deletions and duplications have been shown to be responsible for many developmental syndromes. In several cases, a dosage-sensitive gene mapping to the relevant regions has been implicated as causal. We delve into the mechanisms of HI, especially due to direct protein insufficiency and subunit imbalances in the context of multi-subunit complexes. We show how the nonlinearity inherent to the relationship between genotype and phenotype is responsible for the dominance of the underlying genetic variants. We also explore why increased gene dosage can lead to abnormal phenotypes. Examples include trisomy or segmental genomic duplications in humans and oncogene amplification in cancers. Finally, we examine a few cases of genetic synergy, where the combined effect of two or more variants amplifies their individual effects, underlying a distinguishable phenotype. Further research is required to elucidate the dynamics of multicomponent interactions to unravel the mechanistic complexities of genetic dominance, inter-gene interactions, and their implications for disease.

摘要

在此,我们回顾遗传显性的历史背景和当代见解,重点关注单倍剂量不足(HI),即当基因的仅一个等位基因的功能不足以确保二倍体生物体中的正常表型时的情况。一种相关现象是三倍体敏感性,即当某些“基因”有三个而非两个拷贝时产生的致病效应。当全染色体异常(非整倍体)可与唐氏、爱德华兹和帕陶氏综合征等临床表型相关联时,人们认识到了基因剂量问题在人类中的重要性。随后,更细微的染色体缺失和重复已被证明是许多发育综合征的病因。在一些情况下,定位到相关区域的剂量敏感基因被认为是病因。我们深入探讨单倍剂量不足的机制,特别是由于多亚基复合物背景下直接的蛋白质不足和亚基失衡导致的情况。我们展示了基因型与表型之间关系固有的非线性如何导致潜在遗传变异的显性。我们还探讨了为什么基因剂量增加会导致异常表型。例子包括人类的三体或节段性基因组重复以及癌症中的癌基因扩增。最后,我们研究一些遗传协同作用的案例,其中两个或更多变异的联合效应放大了它们的个体效应,从而产生可区分的表型。需要进一步研究以阐明多组分相互作用的动态过程,从而揭示遗传显性、基因间相互作用的机制复杂性及其对疾病的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d75/12240611/d6a8b14b22cb/JIMD-48-0-g002.jpg

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