Large-scale chromatin organisation in interphase, mitosis and meiosis

被引:10
|
作者
MacGregor, Isobel A. [1 ]
Adams, Ian R. [1 ]
Gilbert, Nick [1 ]
机构
[1] Univ Edinburgh, Western Gen Hosp, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Crewe Rd South, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
3D GENOME ARCHITECTURE; ZINC-FINGER PROTEINS; SYNAPTONEMAL COMPLEX; PSEUDOAUTOSOMAL REGION; MEIOTIC RECOMBINATION; COHESIN SMC1-BETA; CRYOELECTRON MICROSCOPY; MITOTIC PHOSPHORYLATION; MAMMALIAN GENOMES; HIGH-RESOLUTION;
D O I
10.1042/BCJ20180512
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The spatial configuration of chromatin is fundamental to ensure any given cell can fulfil its functional duties, from gene expression to specialised cellular division. Significant technological innovations have facilitated further insights into the structure, function and regulation of three-dimensional chromatin organisation. To date, the vast majority of investigations into chromatin organisation have been conducted in interphase and mitotic cells leaving meiotic chromatin relatively unexplored. In combination, cytological and genome-wide contact frequency analyses in mammalian germ cells have recently demonstrated that large-scale chromatin structures in meiotic prophase I are reminiscent of the sequential loop arrays found in mitotic cells, although interphase-like segmentation of transcriptionally active and inactive regions are also evident along the length of chromosomes. Here, we discuss the similarities and differences of such large-scale chromatin architecture, between interphase, mitotic and meiotic cells, as well as their functional relevance and the proposed modulatory mechanisms which underlie them.
引用
收藏
页码:2141 / 2156
页数:16
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