UR1196 Génomique et Physiologie de la Lactation, INRA, Domaine de Vilvert, F-78352, Jouy-en-Josas, France.
J Mammary Gland Biol Neoplasia. 2010 Mar;15(1):73-83. doi: 10.1007/s10911-010-9169-x. Epub 2010 Feb 10.
During the development of tissues, complex programs take place to reach terminally differentiated states with specific gene expression profiles. Epigenetic regulations such as histone modifications and chromatin condensation have been implicated in the short and long-term control of transcription. It has recently been shown that the 3D spatial organization of chromosomes in the nucleus also plays a role in genome function. Indeed, the eukaryotic interphase nucleus contains sub-domains that are characterized by their enrichment in specific factors such as RNA Polymerase II, splicing machineries or heterochromatin proteins which render portions of the genome differentially permissive to gene expression. The positioning of individual genes relative to these sub-domains is thought to participate in the control of gene expression as an epigenetic mechanism acting in the nuclear space. Here, we review what is known about the sub-nuclear organization of mammary epithelial cells in connection with gene expression and epigenetics. Throughout differentiation, global changes in nuclear architecture occur, notably with respect to heterochromatin distribution. The positions of mammary-specific genes relative to nuclear sub-compartments varies in response to hormonal stimulation. The contribution of tissue architecture to cell differentiation in the mammary gland is also seen at the level of nuclear organization, which is sensitive to microenvironmental stimuli such as extracellular matrix signaling. In addition, alterations in nuclear organization are concomitant with immortalization and carcinogenesis. Thus, the fate of cells appears to be controlled by complex pathways connecting external signal integration, gene expression, epigenetic modifications and chromatin organization in the nucleus.
在组织发育过程中,会发生复杂的程序以达到具有特定基因表达谱的终末分化状态。表观遗传调控,如组蛋白修饰和染色质凝聚,已被牵涉到转录的短期和长期控制中。最近已经表明,染色体在核中的 3D 空间组织也在基因组功能中起作用。事实上,真核细胞间期核包含亚域,其特征在于它们富含特定因子,如 RNA 聚合酶 II、剪接机制或异染色质蛋白,使基因组的部分区域对基因表达具有不同的许可性。相对于这些亚域的个别基因的定位被认为参与基因表达的控制,作为核空间中的一种表观遗传机制。在这里,我们回顾了与基因表达和表观遗传学有关的乳腺上皮细胞的亚核组织的已知情况。在整个分化过程中,核结构发生全局变化,特别是异染色质分布。乳腺特异性基因相对于核亚区的位置因激素刺激而变化。组织架构对乳腺中细胞分化的贡献也在核组织水平上可见,核组织对细胞外基质信号等微环境刺激敏感。此外,核组织的改变伴随着永生化和癌变。因此,细胞的命运似乎受到连接外部信号整合、基因表达、表观遗传修饰和核内染色质组织的复杂途径的控制。