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Quantitative multiplexed imaging of chromatin ultrastructure with Decode-PAINT

View ORCID ProfileHiroshi M. Sasaki, Jocelyn Y. Kishi, Chao-ting Wu, View ORCID ProfileBrian J. Beliveau, View ORCID ProfilePeng Yin
doi: https://doi.org/10.1101/2022.08.01.502089
Hiroshi M. Sasaki
1Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA
2Department of Systems Biology, Harvard Medical School, Boston, MA
410x Genomics, Pleasanton, CA
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  • ORCID record for Hiroshi M. Sasaki
Jocelyn Y. Kishi
1Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA
2Department of Systems Biology, Harvard Medical School, Boston, MA
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Chao-ting Wu
1Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA
3Department of Genetics, Harvard Medical School, Boston, MA
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Brian J. Beliveau
1Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA
2Department of Systems Biology, Harvard Medical School, Boston, MA
5Department of Genome Sciences, University of Washington, Seattle, WA
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  • For correspondence: peng_yin@hms.harvard.edu
Peng Yin
1Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA
2Department of Systems Biology, Harvard Medical School, Boston, MA
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  • ORCID record for Peng Yin
  • For correspondence: peng_yin@hms.harvard.edu
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Abstract

Super-resolution chromatin imaging techniques are emerging as powerful tools for spatial genomics. However, it remains challenging to visualize the genome on the order of tens of nanometers, a scale that can reveal rich structural detail about the nuclear organization. Here we introduce Decode-PAINT, a multiplexed in situ method, which leverages rapid diffraction-limited pre-decoding and DNA-PAINT (DNA points accumulation for imaging nanoscale topography). Decode-PAINT visualizes multiple discrete genomic regions at a resolution close to the nucleosome scale with a simple and easy-to-implement optical setup, reduces total imaging time by omitting multiple rounds of single-molecule recording, and enables the interrogation of the ultrastructure of the targets with <12 nm lateral and <20 nm axial resolution. We showcase the ability of our approach to perform multiplexed, high-resolution profiling of chromatin structure by performing targeted imaging of nine regions of active and inactive X chromosomes in individual cells. In short, Decode-PAINT accelerates in situ structural genomics.

Competing Interest Statement

P.Y. is a cofounder of Ultivue, Inc., NuProbe Global, and Torus Biosystems, Inc. P.Y. holds patents on DNA-PAINT and SABER and related technologies, and is a co-founder and director of Ultivue, Inc., NuProbe Global, Torus Biosystems, Inc., 3EO Health, Spear Bio Inc, and Digital Biology Inc. J.Y.K. and B.J.B. hold patents on SABER.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted August 03, 2022.
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Quantitative multiplexed imaging of chromatin ultrastructure with Decode-PAINT
Hiroshi M. Sasaki, Jocelyn Y. Kishi, Chao-ting Wu, Brian J. Beliveau, Peng Yin
bioRxiv 2022.08.01.502089; doi: https://doi.org/10.1101/2022.08.01.502089
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Quantitative multiplexed imaging of chromatin ultrastructure with Decode-PAINT
Hiroshi M. Sasaki, Jocelyn Y. Kishi, Chao-ting Wu, Brian J. Beliveau, Peng Yin
bioRxiv 2022.08.01.502089; doi: https://doi.org/10.1101/2022.08.01.502089

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