Visualizing DNA folding and RNA in embryos at single-cell resolution

被引:0
|
作者
Leslie J. Mateo
Sedona E. Murphy
Antonina Hafner
Isaac S. Cinquini
Carly A. Walker
Alistair N. Boettiger
机构
[1] Stanford University,Department of Developmental Biology
[2] Stanford University,Department of Genetics
[3] Stanford University,Department of Computer Science
来源
Nature | 2019年 / 568卷
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摘要
The establishment of cell types during development requires precise interactions between genes and distal regulatory sequences. We have a limited understanding of how these interactions look in three dimensions, vary across cell types in complex tissue, and relate to transcription. Here we describe optical reconstruction of chromatin architecture (ORCA), a method that can trace the DNA path in single cells with nanoscale accuracy and genomic resolution reaching two kilobases. We used ORCA to study a Hox gene cluster in cryosectioned Drosophila embryos and labelled around 30 RNA species in parallel. We identified cell-type-specific physical borders between active and Polycomb-repressed DNA, and unexpected Polycomb-independent borders. Deletion of Polycomb-independent borders led to ectopic enhancer–promoter contacts, aberrant gene expression, and developmental defects. Together, these results illustrate an approach for high-resolution, single-cell DNA domain analysis in vivo, identify domain structures that change with cell identity, and show that border elements contribute to the formation of physical domains in Drosophila.
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页码:49 / 54
页数:5
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