Abstract

Specific interactions of the genome with the nuclear lamina (NL) are thought to assist chromosome folding inside the nucleus and to contribute to the regulation of gene expression. High-resolution mapping has recently identified hundreds of large, sharply defined lamina-associated domains (LADs) in the human genome, and suggested that the insulator protein CTCF may help to demarcate these domains. Here, we report the detailed structure of LADs in Drosophila cells, and investigate the putative roles of five insulator proteins in LAD organization. We found that the Drosophila genome is also organized in discrete LADs, which are about five times smaller than human LADs but contain on average a similar number of genes. Systematic comparison to new and published insulator binding maps shows that only SU(HW) binds preferentially at LAD borders and at specific positions inside LADs, while GAF, CTCF, BEAF-32 and DWG are mostly absent from these regions. By knockdown and overexpression studies we demonstrate that SU(HW) weakens genome – NL interactions through a local antagonistic effect, but we did not obtain evidence that it is essential for border formation. Our results provide insights into the evolution of LAD organization and identify SU(HW) as a fine-tuner of genome – NL interactions.

Highlights

  • The nuclear lamina (NL), a dense fibrillar network covering the inside of the nuclear membrane in metazoan cells [reviewed in 1], is thought to represent a major structural element for the nuclear organization of the genome

  • Lamina Associated Domains (LADs) in the Drosophila genome A previous DamID study in Drosophila Kc cells identified hundreds of genes that associate with the NL [7]

  • Previous comparisons to fluoresence in situ hybridization data have indicated that DamID signals obtained with LAM can be interpreted as relative molecular contact frequencies between the NL and the probed genomic locus [7,8]

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Summary

Introduction

The nuclear lamina (NL), a dense fibrillar network covering the inside of the nuclear membrane in metazoan cells [reviewed in 1], is thought to represent a major structural element for the nuclear organization of the genome. Genome-wide mapping using the DamID technology [6] in Drosophila Kc cells demonstrated hundreds of genes to be in molecular contact with the NL [7] These genes are strongly repressed and lack active histone marks. Application of the same mapping technology at a higher resolution in human lung fibroblasts showed that NL interactions occur through large continuous genomic domains with sharply defined borders [8]. In these Lamina Associated Domains (LADs) gene expression is strongly repressed, RNA Polymerase II (RNApolII) and active histone marks are depleted, and repressive histone marks are enriched

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