Chandler Christopher H
Department of Biological Sciences, State University of New York at Oswego, Oswego, New York.
Ann N Y Acad Sci. 2017 Feb;1389(1):37-51. doi: 10.1111/nyas.13307. Epub 2017 Jan 18.
In many species, sex is determined by sex chromosomes, and the sex-specific chromosome (Y or W) stops recombining until it degenerates and carries fewer genes than its recombining counterpart (X or Z). This creates an imbalance in the dosage of most sex-linked genes between males and females. Early work in model organisms demonstrated that X chromosomes in multiple groups independently evolved regulatory mechanisms maintaining balanced expression of X-linked genes. However, recent studies have shown that these dosage compensation mechanisms are far from universal. It remains unclear why dosage compensation mechanisms evolved in some groups of organisms and not others. Two factors have led to confusion in this area: first, different authors sometimes define dosage compensation in different ways; second, dosage compensation is sometimes viewed as an all-or-nothing phenomenon, even though it may vary across cell types, developmental stages, and different classes of genes. Here, I discuss current approaches to testing for sex chromosome dosage compensation and highlight patterns in the phylogenetic distribution of dosage compensation mechanisms and possible explanations for those patterns. I conclude by outlining how the presence of dosage compensation can be tested in nearly any nonmodel organism and provide some recommendations for future studies.
在许多物种中,性别由性染色体决定,而特定性别的染色体(Y或W)在退化之前停止重组,且携带的基因比其重组对应物(X或Z)少。这导致雄性和雌性之间大多数性连锁基因的剂量失衡。模式生物的早期研究表明,多个群体中的X染色体独立进化出调节机制,以维持X连锁基因的平衡表达。然而,最近的研究表明,这些剂量补偿机制远非普遍存在。目前尚不清楚为什么剂量补偿机制在某些生物群体中进化而在其他生物群体中没有。有两个因素导致了该领域的混乱:第一,不同作者有时以不同方式定义剂量补偿;第二,剂量补偿有时被视为一种非此即彼的现象,尽管它可能因细胞类型、发育阶段和不同类别的基因而有所不同。在这里,我讨论了当前检测性染色体剂量补偿的方法,强调了剂量补偿机制系统发育分布中的模式以及对这些模式的可能解释。最后,我概述了如何在几乎任何非模式生物中检测剂量补偿的存在,并为未来的研究提供了一些建议。