Howard Hughes Medical Institute; Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Nat Rev Genet. 2017 Jun;18(6):377-389. doi: 10.1038/nrg.2017.17. Epub 2017 May 8.
Extensive 3D folding is required to package a genome into the tiny nuclear space, and this packaging must be compatible with proper gene expression. Thus, in the well-hierarchized nucleus, chromosomes occupy discrete territories and adopt specific 3D organizational structures that facilitate interactions between regulatory elements for gene expression. The mammalian X chromosome exemplifies this structure-function relationship. Recent studies have shown that, upon X-chromosome inactivation, active and inactive X chromosomes localize to different subnuclear positions and adopt distinct chromosomal architectures that reflect their activity states. Here, we review the roles of long non-coding RNAs, chromosomal organizational structures and the subnuclear localization of chromosomes as they relate to X-linked gene expression.
广泛的 3D 折叠是将基因组包装到微小的核空间中所必需的,这种包装必须与适当的基因表达兼容。因此,在高度分层的细胞核中,染色体占据离散的区域,并采用特定的 3D 组织结构,促进基因表达调控元件之间的相互作用。哺乳动物 X 染色体就是这种结构-功能关系的一个例子。最近的研究表明,在 X 染色体失活后,活性和非活性 X 染色体定位于不同的亚核位置,并采用不同的染色体结构,反映它们的活性状态。在这里,我们回顾了长非编码 RNA、染色体组织结构以及染色体的亚核定位在 X 连锁基因表达中的作用。