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Nuclear RNA-seq of single neurons reveals molecular signatures of activation

Author

Listed:
  • Benjamin Lacar

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Sara B. Linker

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Baptiste N. Jaeger

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Suguna Rani Krishnaswami

    (J. Craig Venter Institute)

  • Jerika J. Barron

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Martijn J. E. Kelder

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Sarah L. Parylak

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Apuã C. M. Paquola

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Pratap Venepally

    (J. Craig Venter Institute)

  • Mark Novotny

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Carolyn O'Connor

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Conor Fitzpatrick

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Jennifer A. Erwin

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Jonathan Y. Hsu

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • David Husband

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Michael J. McConnell

    (University of Virginia School of Medicine)

  • Roger Lasken

    (J. Craig Venter Institute)

  • Fred H. Gage

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

Abstract

Single-cell sequencing methods have emerged as powerful tools for identification of heterogeneous cell types within defined brain regions. Application of single-cell techniques to study the transcriptome of activated neurons can offer insight into molecular dynamics associated with differential neuronal responses to a given experience. Through evaluation of common whole-cell and single-nuclei RNA-sequencing (snRNA-seq) methods, here we show that snRNA-seq faithfully recapitulates transcriptional patterns associated with experience-driven induction of activity, including immediate early genes (IEGs) such as Fos, Arc and Egr1. SnRNA-seq of mouse dentate granule cells reveals large-scale changes in the activated neuronal transcriptome after brief novel environment exposure, including induction of MAPK pathway genes. In addition, we observe a continuum of activation states, revealing a pseudotemporal pattern of activation from gene expression alone. In summary, snRNA-seq of activated neurons enables the examination of gene expression beyond IEGs, allowing for novel insights into neuronal activation patterns in vivo.

Suggested Citation

  • Benjamin Lacar & Sara B. Linker & Baptiste N. Jaeger & Suguna Rani Krishnaswami & Jerika J. Barron & Martijn J. E. Kelder & Sarah L. Parylak & Apuã C. M. Paquola & Pratap Venepally & Mark Novotny & Ca, 2016. "Nuclear RNA-seq of single neurons reveals molecular signatures of activation," Nature Communications, Nature, vol. 7(1), pages 1-13, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11022
    DOI: 10.1038/ncomms11022
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    Cited by:

    1. Marco D. Carpenter & Delaney K. Fischer & Shuo Zhang & Allison M. Bond & Kyle S. Czarnecki & Morgan T. Woolf & Hongjun Song & Elizabeth A. Heller, 2022. "Cell-type specific profiling of histone post-translational modifications in the adult mouse striatum," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Yann Vanrobaeys & Utsav Mukherjee & Lucy Langmack & Stacy E. Beyer & Ethan Bahl & Li-Chun Lin & Jacob J. Michaelson & Ted Abel & Snehajyoti Chatterjee, 2023. "Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    3. Ruth Styfhals & Grygoriy Zolotarov & Gert Hulselmans & Katina I. Spanier & Suresh Poovathingal & Ali M. Elagoz & Seppe Winter & Astrid Deryckere & Nikolaus Rajewsky & Giovanna Ponte & Graziano Fiorito, 2022. "Cell type diversity in a developing octopus brain," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    4. Kaya J. E. Matson & Daniel E. Russ & Claudia Kathe & Isabelle Hua & Dragan Maric & Yi Ding & Jonathan Krynitsky & Randall Pursley & Anupama Sathyamurthy & Jordan W. Squair & Boaz P. Levi & Gregoire Co, 2022. "Single cell atlas of spinal cord injury in mice reveals a pro-regenerative signature in spinocerebellar neurons," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    5. Zachary V. Johnson & Brianna E. Hegarty & George W. Gruenhagen & Tucker J. Lancaster & Patrick T. McGrath & Jeffrey T. Streelman, 2023. "Cellular profiling of a recently-evolved social behavior in cichlid fishes," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    6. Manvendra Singh & Ying Zhao & Vinicius Daguano Gastaldi & Sonja M. Wojcik & Yasmina Curto & Riki Kawaguchi & Ricardo M. Merino & Laura Fernandez Garcia-Agudo & Holger Taschenberger & Nils Brose & Dani, 2023. "Erythropoietin re-wires cognition-associated transcriptional networks," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    7. Vishnu Muraleedharan Saraswathy & Lili Zhou & Mayssa H. Mokalled, 2024. "Single-cell analysis of innate spinal cord regeneration identifies intersecting modes of neuronal repair," Nature Communications, Nature, vol. 15(1), pages 1-21, December.

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