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肢体发育中 HoxD 染色质拓扑的前后差异。

Anterior-posterior differences in HoxD chromatin topology in limb development.

机构信息

MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Crewe Road, Edinburgh EH4 2XU, UK.

出版信息

Development. 2012 Sep;139(17):3157-67. doi: 10.1242/dev.081174.

DOI:10.1242/dev.081174
PMID:22872084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3413162/
Abstract

A late phase of HoxD activation is crucial for the patterning and growth of distal structures across the anterior-posterior (A-P) limb axis of mammals. Polycomb complexes and chromatin compaction have been shown to regulate Hox loci along the main body axis in embryonic development, but the extent to which they have a role in limb-specific HoxD expression, an evolutionary adaptation defined by the activity of distal enhancer elements that drive expression of 5' Hoxd genes, has yet to be fully elucidated. We reveal two levels of chromatin topology that differentiate distal limb A-P HoxD activity. Using both immortalised cell lines derived from posterior and anterior regions of distal E10.5 mouse limb buds, and analysis in E10.5 dissected limb buds themselves, we show that there is a loss of polycomb-catalysed H3K27me3 histone modification and a chromatin decompaction over HoxD in the distal posterior limb compared with anterior. Moreover, we show that the global control region (GCR) long-range enhancer spatially colocalises with the 5' HoxD genomic region specifically in the distal posterior limb. This is consistent with the formation of a chromatin loop between 5' HoxD and the GCR regulatory module at the time and place of distal limb bud development when the GCR participates in initiating Hoxd gene quantitative collinearity and Hoxd13 expression. This is the first example of A-P differences in chromatin compaction and chromatin looping in the development of the mammalian secondary body axis (limb).

摘要

HoxD 激活的晚期阶段对于哺乳动物前后(A-P)肢体轴上远端结构的模式形成和生长至关重要。多梳复合物和染色质紧缩已被证明可在胚胎发育过程中调节主身体轴上的 Hox 基因座,但它们在多大程度上参与了肢体特异性 HoxD 表达(通过驱动 5' Hoxd 基因表达的远端增强子元件的活性定义的进化适应)仍有待充分阐明。我们揭示了区分远端肢体 A-P HoxD 活性的两种染色质拓扑结构。我们使用源自远端 E10.5 小鼠肢芽后区和前区的永生化细胞系,以及对 E10.5 解剖肢芽本身的分析,表明与前区相比,远端后肢的多梳催化 H3K27me3 组蛋白修饰和染色质松解丢失。此外,我们表明全局控制区(GCR)长距离增强子在空间上与 5' HoxD 基因组区域特异性共定位在远端后肢。这与在远端肢芽发育时和在 GCR 参与启动 Hoxd 基因定量共线性和 Hoxd13 表达时,5' HoxD 和 GCR 调控模块之间形成染色质环是一致的。这是哺乳动物次生体轴(肢体)发育中染色质紧缩和染色质环形成的第一个 A-P 差异的例子。

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