Department of Biological Sciences & Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA 24061, USA.
Epigenomics. 2019 Dec;11(16):1827-1837. doi: 10.2217/epi-2019-0135. Epub 2019 Nov 22.
Aneuploidy (i.e., abnormal chromosome number) is the leading cause of miscarriage and congenital defects in humans. Moreover, aneuploidy is ubiquitous in cancer. The deleterious phenotypes associated with aneuploidy are likely a result of the imbalance in the levels of gene products derived from the additional chromosome(s). Here, we summarize the current knowledge on how the presence of extra chromosomes impacts gene expression. We describe studies that have found a strict correlation between gene dosage and transcript levels as wells as studies that have found a less stringent correlation, hinting at the possible existence of dosage compensation mechanisms. We conclude by peering into the epigenetic changes found in aneuploid cells and outlining current knowledge gaps and potential areas of future investigation.
非整倍体(即染色体数目异常)是人类流产和先天性缺陷的主要原因。此外,非整倍体在癌症中普遍存在。与非整倍体相关的有害表型可能是由于额外染色体(多个)上基因产物水平的失衡所致。在这里,我们总结了目前关于额外染色体的存在如何影响基因表达的知识。我们描述了发现基因剂量与转录水平之间存在严格相关性的研究,以及发现相关性较弱的研究,这表明可能存在剂量补偿机制。最后,我们着眼于非整倍体细胞中发现的表观遗传变化,并概述了当前的知识空白和未来可能的研究领域。