Cargando…
Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation
Recent transcriptional profiling technologies are uncovering previously-undefined cell populations and molecular markers at an unprecedented pace. While single cell RNA (scRNA) sequencing is an attractive approach for unbiased transcriptional profiling of all cell types, a complementary method to is...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901332/ https://www.ncbi.nlm.nih.gov/pubmed/31815670 http://dx.doi.org/10.7554/eLife.51452 |
_version_ | 1783477478561415168 |
---|---|
author | Amamoto, Ryoji Garcia, Mauricio D West, Emma R Choi, Jiho Lapan, Sylvain W Lane, Elizabeth A Perrimon, Norbert Cepko, Constance L |
author_facet | Amamoto, Ryoji Garcia, Mauricio D West, Emma R Choi, Jiho Lapan, Sylvain W Lane, Elizabeth A Perrimon, Norbert Cepko, Constance L |
author_sort | Amamoto, Ryoji |
collection | PubMed |
description | Recent transcriptional profiling technologies are uncovering previously-undefined cell populations and molecular markers at an unprecedented pace. While single cell RNA (scRNA) sequencing is an attractive approach for unbiased transcriptional profiling of all cell types, a complementary method to isolate and sequence specific cell populations from heterogeneous tissue remains challenging. Here, we developed Probe-Seq, which allows deep transcriptional profiling of specific cell types isolated using RNA as the defining feature. Dissociated cells are labeled using fluorescent in situ hybridization (FISH) for RNA, and then isolated by fluorescent activated cell sorting (FACS). We used Probe-Seq to purify and profile specific cell types from mouse, human, and chick retinas, as well as from Drosophila midguts. Probe-Seq is compatible with frozen nuclei, making cell types within archival tissue immediately accessible. As it can be multiplexed, combinations of markers can be used to create specificity. Multiplexing also allows for the isolation of multiple cell types from one cell preparation. Probe-Seq should enable RNA profiling of specific cell types from any organism. |
format | Online Article Text |
id | pubmed-6901332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69013322019-12-11 Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation Amamoto, Ryoji Garcia, Mauricio D West, Emma R Choi, Jiho Lapan, Sylvain W Lane, Elizabeth A Perrimon, Norbert Cepko, Constance L eLife Genetics and Genomics Recent transcriptional profiling technologies are uncovering previously-undefined cell populations and molecular markers at an unprecedented pace. While single cell RNA (scRNA) sequencing is an attractive approach for unbiased transcriptional profiling of all cell types, a complementary method to isolate and sequence specific cell populations from heterogeneous tissue remains challenging. Here, we developed Probe-Seq, which allows deep transcriptional profiling of specific cell types isolated using RNA as the defining feature. Dissociated cells are labeled using fluorescent in situ hybridization (FISH) for RNA, and then isolated by fluorescent activated cell sorting (FACS). We used Probe-Seq to purify and profile specific cell types from mouse, human, and chick retinas, as well as from Drosophila midguts. Probe-Seq is compatible with frozen nuclei, making cell types within archival tissue immediately accessible. As it can be multiplexed, combinations of markers can be used to create specificity. Multiplexing also allows for the isolation of multiple cell types from one cell preparation. Probe-Seq should enable RNA profiling of specific cell types from any organism. eLife Sciences Publications, Ltd 2019-12-09 /pmc/articles/PMC6901332/ /pubmed/31815670 http://dx.doi.org/10.7554/eLife.51452 Text en © 2019, Amamoto et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genetics and Genomics Amamoto, Ryoji Garcia, Mauricio D West, Emma R Choi, Jiho Lapan, Sylvain W Lane, Elizabeth A Perrimon, Norbert Cepko, Constance L Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation |
title | Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation |
title_full | Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation |
title_fullStr | Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation |
title_full_unstemmed | Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation |
title_short | Probe-Seq enables transcriptional profiling of specific cell types from heterogeneous tissue by RNA-based isolation |
title_sort | probe-seq enables transcriptional profiling of specific cell types from heterogeneous tissue by rna-based isolation |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901332/ https://www.ncbi.nlm.nih.gov/pubmed/31815670 http://dx.doi.org/10.7554/eLife.51452 |
work_keys_str_mv | AT amamotoryoji probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT garciamauriciod probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT westemmar probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT choijiho probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT lapansylvainw probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT laneelizabetha probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT perrimonnorbert probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation AT cepkoconstancel probeseqenablestranscriptionalprofilingofspecificcelltypesfromheterogeneoustissuebyrnabasedisolation |