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All-viral tracing of monosynaptic inputs to single birthdate-defined neurons in the intact brain

View ORCID ProfileR Irene Jacobsen, View ORCID ProfileRajeevkumar R Nair, View ORCID ProfileHorst A Obenhaus, View ORCID ProfileFlavio Donato, View ORCID ProfileTorstein Slettmoen, View ORCID ProfileMay-Britt Moser, View ORCID ProfileEdvard I Moser
doi: https://doi.org/10.1101/2021.10.18.464781
R Irene Jacobsen
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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  • For correspondence: ragnhild.i.jacobsen@ntnu.no edvard.moser@ntnu.no
Rajeevkumar R Nair
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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Horst A Obenhaus
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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Flavio Donato
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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Torstein Slettmoen
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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May-Britt Moser
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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Edvard I Moser
Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU, Trondheim, 7030, Norway
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  • ORCID record for Edvard I Moser
  • For correspondence: ragnhild.i.jacobsen@ntnu.no edvard.moser@ntnu.no
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Summary

Neuronal firing patterns are the result of inputs converging onto single cells. Identifying these inputs, anatomically and functionally, is essential to understand how neurons integrate information. Single-cell electroporation of helper genes and subsequent local injection of recombinant rabies viruses enable precise mapping of inputs to individual cells in superficial layers of the intact cortex. However, access to neurons in deeper structures requires more invasive procedures, including removal of overlying tissue. We have developed a method that through a combination of virus injections allows us to target ≤4 hippocampal cells 48% of the time and a single cell 16% of the time in wildtype mice without the use of electroporation or tissue aspiration. We identify local and distant monosynaptic inputs that can be functionally characterised in vivo. By expanding the toolbox for monosynaptic circuit tracing, this method will help further our understanding of neuronal integration at the level of single cells.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Lead contact: Edvard I. Moser, edvard.moser{at}ntnu.no

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 October 19, 2021.
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All-viral tracing of monosynaptic inputs to single birthdate-defined neurons in the intact brain
R Irene Jacobsen, Rajeevkumar R Nair, Horst A Obenhaus, Flavio Donato, Torstein Slettmoen, May-Britt Moser, Edvard I Moser
bioRxiv 2021.10.18.464781; doi: https://doi.org/10.1101/2021.10.18.464781
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All-viral tracing of monosynaptic inputs to single birthdate-defined neurons in the intact brain
R Irene Jacobsen, Rajeevkumar R Nair, Horst A Obenhaus, Flavio Donato, Torstein Slettmoen, May-Britt Moser, Edvard I Moser
bioRxiv 2021.10.18.464781; doi: https://doi.org/10.1101/2021.10.18.464781

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