Mehta Ishita S, Figgitt Martin, Clements Craig S, Kill Ian R, Bridger Joanna M
Laboratory of Nuclear and Genomic Health, Centre for Cell and Chromosome Biology, Biosciences, School of Health Sciences and Social Care, Brunel University, West London, UB8 3PH, UK.
Ann N Y Acad Sci. 2007 Apr;1100:250-63. doi: 10.1196/annals.1395.027.
The organization of the genome within interphase nuclei, and how it interacts with nuclear structures is important for the regulation of nuclear functions. Many of the studies researching the importance of genome organization and nuclear structure are performed in young, proliferating, and often transformed cells. These studies do not reveal anything about the nucleus or genome in nonproliferating cells, which may be relevant for the regulation of both proliferation and replicative senescence. Here, we provide an overview of what is known about the genome and nuclear structure in senescent cells. We review the evidence that nuclear structures, such as the nuclear lamina, nucleoli, the nuclear matrix, nuclear bodies (such as promyelocytic leukemia bodies), and nuclear morphology all become altered within growth-arrested or senescent cells. Specific alterations to the genome in senescent cells, as compared to young proliferating cells, are described, including aneuploidy, chromatin modifications, chromosome positioning, relocation of heterochromatin, and changes to telomeres.
基因组在间期细胞核内的组织方式以及它如何与核结构相互作用对于核功能的调节至关重要。许多研究基因组组织和核结构重要性的实验是在年轻的、增殖的且通常是转化细胞中进行的。这些研究没有揭示任何关于非增殖细胞中细胞核或基因组的信息,而这些信息可能与增殖和复制性衰老的调节相关。在这里,我们概述了关于衰老细胞中基因组和核结构的已知情况。我们回顾了以下证据:核结构,如核纤层、核仁、核基质、核体(如早幼粒细胞白血病小体)以及核形态在生长停滞或衰老细胞中都会发生改变。与年轻的增殖细胞相比,衰老细胞中基因组的特定改变也被描述,包括非整倍体、染色质修饰、染色体定位、异染色质的重新定位以及端粒的变化。