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Engineering inducible biomolecular assemblies for genome imaging and manipulation in living cells

Author

Listed:
  • Qin Peng

    (University of California
    Institute of Systems and Physical Biology, Shenzhen Bay Laboratory)

  • Ziliang Huang

    (University of California)

  • Kun Sun

    (Institute of Cancer Research, Shenzhen Bay Laboratory)

  • Yahan Liu

    (University of California)

  • Chi Woo Yoon

    (University of California)

  • Reed E. S. Harrison

    (University of California)

  • Danielle L. Schmitt

    (University of California)

  • Linshan Zhu

    (University of California)

  • Yiqian Wu

    (University of California)

  • Ipek Tasan

    (University of Illinois at Urbana-Champaign)

  • Huimin Zhao

    (University of Illinois at Urbana-Champaign
    University of Illinois, Urbana-Champaign)

  • Jin Zhang

    (University of California)

  • Sheng Zhong

    (University of California)

  • Shu Chien

    (University of California
    University of California)

  • Yingxiao Wang

    (University of California)

Abstract

Genome architecture and organization play critical roles in cell life. However, it remains largely unknown how genomic loci are dynamically coordinated to regulate gene expression and determine cell fate at the single cell level. We have developed an inducible system which allows Simultaneous Imaging and Manipulation of genomic loci by Biomolecular Assemblies (SIMBA) in living cells. In SIMBA, the human heterochromatin protein 1α (HP1α) is fused to mCherry and FRB, which can be induced to form biomolecular assemblies (BAs) with FKBP-scFv, guided to specific genomic loci by a nuclease-defective Cas9 (dCas9) or a transcriptional factor (TF) carrying tandem repeats of SunTag. The induced BAs can not only enhance the imaging signals at target genomic loci using a single sgRNA, either at repetitive or non-repetitive sequences, but also recruit epigenetic modulators such as histone methyltransferase SUV39H1 to locally repress transcription. As such, SIMBA can be applied to simultaneously visualize and manipulate, in principle, any genomic locus with controllable timing in living cells.

Suggested Citation

  • Qin Peng & Ziliang Huang & Kun Sun & Yahan Liu & Chi Woo Yoon & Reed E. S. Harrison & Danielle L. Schmitt & Linshan Zhu & Yiqian Wu & Ipek Tasan & Huimin Zhao & Jin Zhang & Sheng Zhong & Shu Chien & Y, 2022. "Engineering inducible biomolecular assemblies for genome imaging and manipulation in living cells," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-35504-x
    DOI: 10.1038/s41467-022-35504-x
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    References listed on IDEAS

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    1. Yao-Cheng Lin & Morgane Boone & Leander Meuris & Irma Lemmens & Nadine Van Roy & Arne Soete & Joke Reumers & Matthieu Moisse & Stéphane Plaisance & Radoje Drmanac & Jason Chen & Frank Speleman & Dieth, 2014. "Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations," Nature Communications, Nature, vol. 5(1), pages 1-12, December.
    2. Yifeng Qi & Bin Zhang, 2021. "Chromatin network retards nucleoli coalescence," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    3. Silvana Konermann & Mark D. Brigham & Alexandro E. Trevino & Julia Joung & Omar O. Abudayyeh & Clea Barcena & Patrick D. Hsu & Naomi Habib & Jonathan S. Gootenberg & Hiroshi Nishimasu & Osamu Nureki &, 2015. "Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex," Nature, Nature, vol. 517(7536), pages 583-588, January.
    4. Baohui Chen & Wei Zou & Haiyue Xu & Ying Liang & Bo Huang, 2018. "Efficient labeling and imaging of protein-coding genes in living cells using CRISPR-Tag," Nature Communications, Nature, vol. 9(1), pages 1-9, December.
    5. Nicholas M. Kanaan & Chelsey Hamel & Tessa Grabinski & Benjamin Combs, 2020. "Liquid-liquid phase separation induces pathogenic tau conformations in vitro," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
    6. Peiwu Qin & Mahmut Parlak & Cem Kuscu & Jigar Bandaria & Mustafa Mir & Karol Szlachta & Ritambhara Singh & Xavier Darzacq & Ahmet Yildiz & Mazhar Adli, 2017. "Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9," Nature Communications, Nature, vol. 8(1), pages 1-10, April.
    7. Amy R. Strom & Alexander V. Emelyanov & Mustafa Mir & Dmitry V. Fyodorov & Xavier Darzacq & Gary H. Karpen, 2017. "Phase separation drives heterochromatin domain formation," Nature, Nature, vol. 547(7662), pages 241-245, July.
    8. Patricia A. Clow & Menghan Du & Nathaniel Jillette & Aziz Taghbalout & Jacqueline J. Zhu & Albert W. Cheng, 2022. "CRISPR-mediated multiplexed live cell imaging of nonrepetitive genomic loci with one guide RNA per locus," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
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