Cargando…
C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool
C. elegans Notch signaling maintains a pool of germline stem cells within their single-celled mesenchymal niche. Here we investigate the Notch transcriptional response in germline stem cells using single-molecule fluorescence in situ hybridization coupled with automated, high-throughput quantitation...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094854/ https://www.ncbi.nlm.nih.gov/pubmed/27705743 http://dx.doi.org/10.7554/eLife.18370 |
_version_ | 1782465183705202688 |
---|---|
author | Lee, ChangHwan Sorensen, Erika B Lynch, Tina R Kimble, Judith |
author_facet | Lee, ChangHwan Sorensen, Erika B Lynch, Tina R Kimble, Judith |
author_sort | Lee, ChangHwan |
collection | PubMed |
description | C. elegans Notch signaling maintains a pool of germline stem cells within their single-celled mesenchymal niche. Here we investigate the Notch transcriptional response in germline stem cells using single-molecule fluorescence in situ hybridization coupled with automated, high-throughput quantitation. This approach allows us to distinguish Notch-dependent nascent transcripts in the nucleus from mature mRNAs in the cytoplasm. We find that Notch-dependent active transcription sites occur in a probabilistic fashion and, unexpectedly, do so in a steep gradient across the stem cell pool. Yet these graded nuclear sites create a nearly uniform field of mRNAs that extends beyond the region of transcriptional activation. Therefore, active transcription sites provide a precise view of where the Notch-dependent transcriptional complex is productively engaged. Our findings offer a new window into the Notch transcriptional response and demonstrate the importance of assaying nascent transcripts at active transcription sites as a readout for canonical signaling. DOI: http://dx.doi.org/10.7554/eLife.18370.001 |
format | Online Article Text |
id | pubmed-5094854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50948542016-11-04 C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool Lee, ChangHwan Sorensen, Erika B Lynch, Tina R Kimble, Judith eLife Cell Biology C. elegans Notch signaling maintains a pool of germline stem cells within their single-celled mesenchymal niche. Here we investigate the Notch transcriptional response in germline stem cells using single-molecule fluorescence in situ hybridization coupled with automated, high-throughput quantitation. This approach allows us to distinguish Notch-dependent nascent transcripts in the nucleus from mature mRNAs in the cytoplasm. We find that Notch-dependent active transcription sites occur in a probabilistic fashion and, unexpectedly, do so in a steep gradient across the stem cell pool. Yet these graded nuclear sites create a nearly uniform field of mRNAs that extends beyond the region of transcriptional activation. Therefore, active transcription sites provide a precise view of where the Notch-dependent transcriptional complex is productively engaged. Our findings offer a new window into the Notch transcriptional response and demonstrate the importance of assaying nascent transcripts at active transcription sites as a readout for canonical signaling. DOI: http://dx.doi.org/10.7554/eLife.18370.001 eLife Sciences Publications, Ltd 2016-10-05 /pmc/articles/PMC5094854/ /pubmed/27705743 http://dx.doi.org/10.7554/eLife.18370 Text en © 2016, Lee et al 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 | Cell Biology Lee, ChangHwan Sorensen, Erika B Lynch, Tina R Kimble, Judith C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
title | C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
title_full | C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
title_fullStr | C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
title_full_unstemmed | C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
title_short | C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
title_sort | c. elegans glp-1/notch activates transcription in a probability gradient across the germline stem cell pool |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094854/ https://www.ncbi.nlm.nih.gov/pubmed/27705743 http://dx.doi.org/10.7554/eLife.18370 |
work_keys_str_mv | AT leechanghwan celegansglp1notchactivatestranscriptioninaprobabilitygradientacrossthegermlinestemcellpool AT sorensenerikab celegansglp1notchactivatestranscriptioninaprobabilitygradientacrossthegermlinestemcellpool AT lynchtinar celegansglp1notchactivatestranscriptioninaprobabilitygradientacrossthegermlinestemcellpool AT kimblejudith celegansglp1notchactivatestranscriptioninaprobabilitygradientacrossthegermlinestemcellpool |