Gene dosage effects: nonlinearities, genetic interactions, and dosage compensation

被引:101
作者
Veitia, Reiner A. [1 ,2 ]
Bottani, Samuel [2 ,3 ]
Birchler, James A. [4 ]
机构
[1] CNRS, Inst Jacques Monod, UMR7592, Paris, France
[2] Univ Paris 07, Univ Paris Diderot, Paris, France
[3] Univ Paris 07, Paris, France
[4] Univ Missouri, Div Biol Sci, Columbia, MO 65211 USA
关键词
aneuploidy; interactome; gene expression; whole genome duplication; copy number variants; dosage compensation; EXPRESSION; GENOME; DOMINANCE; MAIZE; MUTATIONS; SENSITIVITY; PERSPECTIVE; ANEUPLOIDY; COMPLEXES; NETWORK;
D O I
10.1016/j.tig.2013.04.004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
High-throughput genomic analyses have shown that many mutations, including loss-of-function (LOF) mutations, are present in diseased as well as in healthy individuals. Gene dosage effects due to deletions, duplications, and LOF mutations provide avenues to explore oligo- and multigenic inheritance. Here, we focus on several mechanisms that mediate gene dosage effects and analyze biochemical interactions among multiple gene products that are sources of nonlinear relations connecting genotypes and phenotypes. We also explore potential mechanisms that compensate for gene dosage effects. Understanding these issues is critical to understanding why an individual bearing a few damaging mutations can be severely diseased, whereas others harboring tens of potentially deleterious mutations can appear quite healthy.
引用
收藏
页码:385 / 393
页数:9
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