1. Chromosomes and Gene Expression

Super-resolution imaging of a 2.5 kb non-repetitive DNA in situ in the nuclear genome using molecular beacon probes

  1. Yanxiang Ni  Is a corresponding author
  2. Bo Cao
  3. Tszshan Ma
  4. Gang Niu
  5. Yingdong Huo
  6. Jiandong Huang
  7. Danni Chen
  8. Yi Liu
  9. Bin Yu
  10. Michael Qiwei Zhang  Is a corresponding author
  11. Hanben Niu  Is a corresponding author
  1. College of Optoelectronic Engineering, Shenzhen University, China
  2. Tsinghua University, China
  3. The University of Hong Kong, China
https://doi.org/10.7554/eLife.21660
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Cite this article
  1. Yanxiang Ni
  2. Bo Cao
  3. Tszshan Ma
  4. Gang Niu
  5. Yingdong Huo
  6. Jiandong Huang
  7. Danni Chen
  8. Yi Liu
  9. Bin Yu
  10. Michael Qiwei Zhang
  11. Hanben Niu
(2017)
Super-resolution imaging of a 2.5 kb non-repetitive DNA in situ in the nuclear genome using molecular beacon probes
eLife 6:e21660.
https://doi.org/10.7554/eLife.21660
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  3. Download .RIS

Abstract

High-resolution visualization of short non-repetitive DNA in situ in the nuclear genome is essential for studying looping interactions and chromatin organization in single cells. Recent advances in fluorescence in situ hybridization (FISH) using Oligopaints probes enabled super-resolution imaging of genomic domains with a resolution limit of 4.9 kb. To target shorter elements, we developed a simple FISH method that uses only molecular beacon (MB) probes to facilitate the probe-target binding, while minimizing non-specific fluorescence. We used three-dimensional stochastic optical reconstruction microscopy (3D-STORM) and optimized the imaging conditions to efficiently distinguish sparsely distributed Alexa-647 from background cellular autofluorescence. Utilizing 3D-STORM and 29-34 individual MB probes, we observed 3D fine-scale nanostructures of 2.5 kb integrated or endogenous unique DNA in situ in the human or mouse genome, respectively, demonstrating the capability of MB-based FISH in visualizing a so far shortest and non-repetitive genomic sequence in 3D at super-resolution.

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Article and author information

Author details

  1. Yanxiang Ni

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    For correspondence
    niyanxiang0000@gmail.com
    Competing interests
    The authors declare that no competing interests exist.

  2. Bo Cao

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    Competing interests
    The authors declare that no competing interests exist.

  3. Tszshan Ma

    MOE Key laboratory of Bioinformatics, Tsinghua University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.

  4. Gang Niu

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    Competing interests
    The authors declare that no competing interests exist.

  5. Yingdong Huo

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    Competing interests
    The authors declare that no competing interests exist.

  6. Jiandong Huang

    School of Biomedical Sciences, The University of Hong Kong, Hong Kong, China
    Competing interests
    The authors declare that no competing interests exist.

  7. Danni Chen

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    Competing interests
    The authors declare that no competing interests exist.

  8. Yi Liu

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    Competing interests
    The authors declare that no competing interests exist.

  9. Bin Yu

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    Competing interests
    The authors declare that no competing interests exist.

  10. Michael Qiwei Zhang

    MOE Key laboratory of Bioinformatics, Tsinghua University, Beijing, China
    For correspondence
    michaelzhang@tsinghua.edu.cn
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-7408-1830

  11. Hanben Niu

    Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China
    For correspondence
    hbniu@szu.edu.cn
    Competing interests
    The authors declare that no competing interests exist.

Funding

National Natural Science Foundation of China (61235012)

  • Hanben Niu

National Natural Science Foundation of China (61335001)

  • Michael Qiwei Zhang

Shenzhen Science and Technology Planning Project (JCYJ20150324141711698)

  • Michael Qiwei Zhang

National Natural Science Foundation of China (31401146)

  • Yanxiang Ni

National Natural Science Foundation of China (31361163004)

  • Michael Qiwei Zhang

National Natural Science Foundation of China (91019016)

  • Michael Qiwei Zhang

the National Basic Research Program of China (2012CB825802)

  • Hanben Niu

the Special-Funded Program on National Key Scientific Instruments and Equipment Development (2012YQ150092)

  • Hanben Niu

the National Key Basic Research Project (2012CB316503)

  • Michael Qiwei Zhang

the National Key Basic Research Program of China (2015CB352005)

  • Hanben Niu

National Natural Science Foundation of China (61178080)

  • Michael Qiwei Zhang

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Reviewing Editor

  1. Lothar Schermelleh, University of Oxford, United Kingdom

Version history

  1. Received: September 20, 2016
  2. Accepted: April 24, 2017
  3. Accepted Manuscript published: May 9, 2017 (version 1)
  4. Version of Record published: May 16, 2017 (version 2)

Copyright

© 2017, Ni et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

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  1. Yanxiang Ni
  2. Bo Cao
  3. Tszshan Ma
  4. Gang Niu
  5. Yingdong Huo
  6. Jiandong Huang
  7. Danni Chen
  8. Yi Liu
  9. Bin Yu
  10. Michael Qiwei Zhang
  11. Hanben Niu
(2017)
Super-resolution imaging of a 2.5 kb non-repetitive DNA in situ in the nuclear genome using molecular beacon probes
eLife 6:e21660.
https://doi.org/10.7554/eLife.21660

Share this article

https://doi.org/10.7554/eLife.21660

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