Abstract
Mammalian interphase chromosomes interact with the nuclear lamina (NL) through hundreds of large lamina-associated domains (LADs). We report a method to map NL contacts genome-wide in single human cells. Analysis of nearly 400 maps reveals a core architecture consisting of gene-poor LADs that contact the NL with high cell-to-cell consistency, interspersed by LADs with more variable NL interactions. The variable contacts tend to be cell-type specific and are more sensitive to changes in genome ploidy than the consistent contacts. Single-cell maps indicate that NL contacts involve multivalent interactions over hundreds of kilobases. Moreover, we observe extensive intra-chromosomal coordination of NL contacts, even over tens of megabases. Such coordinated loci exhibit preferential interactions as detected by Hi-C. Finally, the consistency of NL contacts is inversely linked to gene activity in single cells and correlates positively with the heterochromatic histone modification H3K9me3. These results highlight fundamental principles of single-cell chromatin organization. VIDEO ABSTRACT.
| Original language | English |
|---|---|
| Pages (from-to) | 134-47 |
| Number of pages | 14 |
| Journal | Cell |
| Volume | 163 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 24 Sept 2015 |
Keywords
- Cell Line, Tumor
- Chromatin
- Chromosomes
- Genome-Wide Association Study
- Humans
- In Situ Hybridization, Fluorescence
- Interphase
- Nuclear Lamina
- Single-Cell Analysis
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