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DRUG-seq Provides Unbiased Biological Activity Readouts for Neuroscience Drug Discovery
[Image: see text] Unbiased transcriptomic RNA-seq data has provided deep insights into biological processes. However, its impact in drug discovery has been narrow given high costs and low throughput. Proof-of-concept studies with Digital RNA with pertUrbation of Genes (DRUG)-seq demonstrated the pot...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207813/ https://www.ncbi.nlm.nih.gov/pubmed/35508359 http://dx.doi.org/10.1021/acschembio.1c00920 |
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author | Li, Jingyao Ho, Daniel J. Henault, Martin Yang, Chian Neri, Marilisa Ge, Robin Renner, Steffen Mansur, Leandra Lindeman, Alicia Kelly, Brian Tumkaya, Tayfun Ke, Xiaoling Soler-Llavina, Gilberto Shanker, Gopi Russ, Carsten Hild, Marc Gubser Keller, Caroline Jenkins, Jeremy L. Worringer, Kathleen A. Sigoillot, Frederic D. Ihry, Robert J. |
author_facet | Li, Jingyao Ho, Daniel J. Henault, Martin Yang, Chian Neri, Marilisa Ge, Robin Renner, Steffen Mansur, Leandra Lindeman, Alicia Kelly, Brian Tumkaya, Tayfun Ke, Xiaoling Soler-Llavina, Gilberto Shanker, Gopi Russ, Carsten Hild, Marc Gubser Keller, Caroline Jenkins, Jeremy L. Worringer, Kathleen A. Sigoillot, Frederic D. Ihry, Robert J. |
author_sort | Li, Jingyao |
collection | PubMed |
description | [Image: see text] Unbiased transcriptomic RNA-seq data has provided deep insights into biological processes. However, its impact in drug discovery has been narrow given high costs and low throughput. Proof-of-concept studies with Digital RNA with pertUrbation of Genes (DRUG)-seq demonstrated the potential to address this gap. We extended the DRUG-seq platform by subjecting it to rigorous testing and by adding an open-source analysis pipeline. The results demonstrate high reproducibility and ability to resolve the mechanism(s) of action for a diverse set of compounds. Furthermore, we demonstrate how this data can be incorporated into a drug discovery project aiming to develop therapeutics for schizophrenia using human stem cell-derived neurons. We identified both an on-target activation signature, induced by a set of chemically distinct positive allosteric modulators of the N-methyl-d-aspartate (NMDA) receptor, and independent off-target effects. Overall, the protocol and open-source analysis pipeline are a step toward industrializing RNA-seq for high-complexity transcriptomics studies performed at a saturating scale. |
format | Online Article Text |
id | pubmed-9207813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92078132022-06-21 DRUG-seq Provides Unbiased Biological Activity Readouts for Neuroscience Drug Discovery Li, Jingyao Ho, Daniel J. Henault, Martin Yang, Chian Neri, Marilisa Ge, Robin Renner, Steffen Mansur, Leandra Lindeman, Alicia Kelly, Brian Tumkaya, Tayfun Ke, Xiaoling Soler-Llavina, Gilberto Shanker, Gopi Russ, Carsten Hild, Marc Gubser Keller, Caroline Jenkins, Jeremy L. Worringer, Kathleen A. Sigoillot, Frederic D. Ihry, Robert J. ACS Chem Biol [Image: see text] Unbiased transcriptomic RNA-seq data has provided deep insights into biological processes. However, its impact in drug discovery has been narrow given high costs and low throughput. Proof-of-concept studies with Digital RNA with pertUrbation of Genes (DRUG)-seq demonstrated the potential to address this gap. We extended the DRUG-seq platform by subjecting it to rigorous testing and by adding an open-source analysis pipeline. The results demonstrate high reproducibility and ability to resolve the mechanism(s) of action for a diverse set of compounds. Furthermore, we demonstrate how this data can be incorporated into a drug discovery project aiming to develop therapeutics for schizophrenia using human stem cell-derived neurons. We identified both an on-target activation signature, induced by a set of chemically distinct positive allosteric modulators of the N-methyl-d-aspartate (NMDA) receptor, and independent off-target effects. Overall, the protocol and open-source analysis pipeline are a step toward industrializing RNA-seq for high-complexity transcriptomics studies performed at a saturating scale. American Chemical Society 2022-05-04 2022-06-17 /pmc/articles/PMC9207813/ /pubmed/35508359 http://dx.doi.org/10.1021/acschembio.1c00920 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Li, Jingyao Ho, Daniel J. Henault, Martin Yang, Chian Neri, Marilisa Ge, Robin Renner, Steffen Mansur, Leandra Lindeman, Alicia Kelly, Brian Tumkaya, Tayfun Ke, Xiaoling Soler-Llavina, Gilberto Shanker, Gopi Russ, Carsten Hild, Marc Gubser Keller, Caroline Jenkins, Jeremy L. Worringer, Kathleen A. Sigoillot, Frederic D. Ihry, Robert J. DRUG-seq Provides Unbiased Biological Activity Readouts for Neuroscience Drug Discovery |
title | DRUG-seq Provides Unbiased Biological Activity Readouts
for Neuroscience Drug Discovery |
title_full | DRUG-seq Provides Unbiased Biological Activity Readouts
for Neuroscience Drug Discovery |
title_fullStr | DRUG-seq Provides Unbiased Biological Activity Readouts
for Neuroscience Drug Discovery |
title_full_unstemmed | DRUG-seq Provides Unbiased Biological Activity Readouts
for Neuroscience Drug Discovery |
title_short | DRUG-seq Provides Unbiased Biological Activity Readouts
for Neuroscience Drug Discovery |
title_sort | drug-seq provides unbiased biological activity readouts
for neuroscience drug discovery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207813/ https://www.ncbi.nlm.nih.gov/pubmed/35508359 http://dx.doi.org/10.1021/acschembio.1c00920 |
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