4.8 Article

Single-molecule super-resolution imaging of chromosomes and in situ haplotype visualization using Oligopaint FISH probes

Journal

NATURE COMMUNICATIONS
Volume 6, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms8147

Keywords

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Funding

  1. NIH/NIGMS [RO1GM61936, 5DP1GM106412]
  2. Harvard Medical School (HMS)
  3. NIH/NCI [F32CA157188]
  4. Centre National de la Recherche Scientifique
  5. Fulbright Visiting Scholar Program
  6. NIH [1DP2OD007292, 1R01EB018659, 5R21HD072481, 1DP2OD004641, RO1-GM090278]
  7. HHMI
  8. Damon Runyon Cancer Research Foundation
  9. ONR [N000141110914, N000141010827, N000141310593]
  10. NSF [CCF1054898, CCF1162459]
  11. Wyss Institute for Biologically Engineering
  12. Alexander von Humboldt-Foundation
  13. Division of Computing and Communication Foundations
  14. Direct For Computer & Info Scie & Enginr [1317694] Funding Source: National Science Foundation

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Fluorescence in situ hybridization (FISH) is a powerful single-cell technique for studying nuclear structure and organization. Here we report two advances in FISH-based imaging. We first describe the in situ visualization of single-copy regions of the genome using two single-molecule super-resolution methodologies. We then introduce a robust and reliable system that harnesses single-nucleotide polymorphisms (SNPs) to visually distinguish the maternal and paternal homologous chromosomes in mammalian and insect systems. Both of these new technologies are enabled by renewable, bioinformatically designed, oligonucleotide-based Oligopaint probes, which we augment with a strategy that uses secondary oligonucleotides (oligos) to produce and enhance fluorescent signals. These advances should substantially expand the capability to query parent-of-origin-specific chromosome positioning and gene expression on a cell-by-cell basis.

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