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A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell
The sense of smell helps us navigate the environment, but its molecular architecture and underlying logic remain understudied. The spatial location of odorant receptor genes (Olfrs) in the nose is thought to be independent of the structural diversity of the odorants they detect. Using spatial transc...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995392/ https://www.ncbi.nlm.nih.gov/pubmed/35320714 http://dx.doi.org/10.1016/j.celrep.2022.110547 |
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author | Ruiz Tejada Segura, Mayra L. Abou Moussa, Eman Garabello, Elisa Nakahara, Thiago S. Makhlouf, Melanie Mathew, Lisa S. Wang, Li Valle, Filippo Huang, Susie S.Y. Mainland, Joel D. Caselle, Michele Osella, Matteo Lorenz, Stephan Reisert, Johannes Logan, Darren W. Malnic, Bettina Scialdone, Antonio Saraiva, Luis R. |
author_facet | Ruiz Tejada Segura, Mayra L. Abou Moussa, Eman Garabello, Elisa Nakahara, Thiago S. Makhlouf, Melanie Mathew, Lisa S. Wang, Li Valle, Filippo Huang, Susie S.Y. Mainland, Joel D. Caselle, Michele Osella, Matteo Lorenz, Stephan Reisert, Johannes Logan, Darren W. Malnic, Bettina Scialdone, Antonio Saraiva, Luis R. |
author_sort | Ruiz Tejada Segura, Mayra L. |
collection | PubMed |
description | The sense of smell helps us navigate the environment, but its molecular architecture and underlying logic remain understudied. The spatial location of odorant receptor genes (Olfrs) in the nose is thought to be independent of the structural diversity of the odorants they detect. Using spatial transcriptomics, we create a genome-wide 3D atlas of the mouse olfactory mucosa (OM). Topographic maps of genes differentially expressed in space reveal that both Olfrs and non-Olfrs are distributed in a continuous and overlapping fashion over at least five broad zones in the OM. The spatial locations of Olfrs correlate with the mucus solubility of the odorants they recognize, providing direct evidence for the chromatographic theory of olfaction. This resource resolves the molecular architecture of the mouse OM and will inform future studies on mechanisms underlying Olfr gene choice, axonal pathfinding, patterning of the nervous system, and basic logic for the peripheral representation of smell. |
format | Online Article Text |
id | pubmed-8995392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-89953922022-04-11 A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell Ruiz Tejada Segura, Mayra L. Abou Moussa, Eman Garabello, Elisa Nakahara, Thiago S. Makhlouf, Melanie Mathew, Lisa S. Wang, Li Valle, Filippo Huang, Susie S.Y. Mainland, Joel D. Caselle, Michele Osella, Matteo Lorenz, Stephan Reisert, Johannes Logan, Darren W. Malnic, Bettina Scialdone, Antonio Saraiva, Luis R. Cell Rep Article The sense of smell helps us navigate the environment, but its molecular architecture and underlying logic remain understudied. The spatial location of odorant receptor genes (Olfrs) in the nose is thought to be independent of the structural diversity of the odorants they detect. Using spatial transcriptomics, we create a genome-wide 3D atlas of the mouse olfactory mucosa (OM). Topographic maps of genes differentially expressed in space reveal that both Olfrs and non-Olfrs are distributed in a continuous and overlapping fashion over at least five broad zones in the OM. The spatial locations of Olfrs correlate with the mucus solubility of the odorants they recognize, providing direct evidence for the chromatographic theory of olfaction. This resource resolves the molecular architecture of the mouse OM and will inform future studies on mechanisms underlying Olfr gene choice, axonal pathfinding, patterning of the nervous system, and basic logic for the peripheral representation of smell. 2022-03-22 /pmc/articles/PMC8995392/ /pubmed/35320714 http://dx.doi.org/10.1016/j.celrep.2022.110547 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Ruiz Tejada Segura, Mayra L. Abou Moussa, Eman Garabello, Elisa Nakahara, Thiago S. Makhlouf, Melanie Mathew, Lisa S. Wang, Li Valle, Filippo Huang, Susie S.Y. Mainland, Joel D. Caselle, Michele Osella, Matteo Lorenz, Stephan Reisert, Johannes Logan, Darren W. Malnic, Bettina Scialdone, Antonio Saraiva, Luis R. A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
title | A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
title_full | A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
title_fullStr | A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
title_full_unstemmed | A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
title_short | A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
title_sort | 3d transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995392/ https://www.ncbi.nlm.nih.gov/pubmed/35320714 http://dx.doi.org/10.1016/j.celrep.2022.110547 |
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