Herbomel P
Département de Biologie Moléculaire, Institut Pasteur, Paris, France.
New Biol. 1990 Nov;2(11):937-45.
In higher eukaryotes, gene activation is accompanied by an increased sensitivity to DNaseI over a domain that extends beyond the limits of the gene itself, or of the gene cluster to which it belongs. This increased sensitivity probably reflects both the partial decondensation of chromatin and an increased communication with the outside of the nucleus. In addition, gene activation usually causes a coreplication domain that extends much beyond the decondensation domain to switch to an early replication time in S phase. This switch is produced, at least in some cases, by an early firing of origins of replication situated in flanking condensed chromatin. Some of the recently identified DNA domains that tether chromosomal loops to the nuclear matrix do represent the borders of decondensation domains. They may also constitute pausing sites for replication forks. The different replication times of successive 200- to 400-kb regions along the genome may have been the basis for the observed long-term differentiation of very large genomes in domains of different overall sequence composition (G:C content and distribution of short repeated motifs). Chromosomal bands represent a low resolution picture of this pattern. Just like gene methylation, differential replication timing and the consequent compositional differentiation of the genome have probably contributed to making the management of very large genomes workable.
在高等真核生物中,基因激活伴随着在一个超出基因本身或其所属基因簇界限的区域内对DNaseI敏感性的增加。这种敏感性增加可能既反映了染色质的部分解聚,也反映了与细胞核外部交流的增加。此外,基因激活通常会使一个延伸到解聚域之外的共复制域在S期切换到早期复制时间。这种切换至少在某些情况下是由位于侧翼凝聚染色质中的复制起点的早期启动产生的。最近确定的一些将染色体环系于核基质的DNA结构域确实代表了解聚域的边界。它们也可能构成复制叉的暂停位点。沿着基因组连续的200至400kb区域的不同复制时间可能是观察到的非常大的基因组在不同总体序列组成(G:C含量和短重复基序分布)的结构域中长期分化的基础。染色体带代表了这种模式的低分辨率图像。就像基因甲基化一样,差异复制时间以及随之而来的基因组组成分化可能有助于使非常大的基因组的管理变得可行。