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Repression by PRDM13 is critical for generating precision in neuronal identity
The mechanisms that activate some genes while silencing others are critical to ensure precision in lineage specification as multipotent progenitors become restricted in cell fate. During neurodevelopment, these mechanisms are required to generate the diversity of neuronal subtypes found in the nervo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576485/ https://www.ncbi.nlm.nih.gov/pubmed/28850031 http://dx.doi.org/10.7554/eLife.25787 |
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author | Mona, Bishakha Uruena, Ana Kollipara, Rahul K Ma, Zhenzhong Borromeo, Mark D Chang, Joshua C Johnson, Jane E |
author_facet | Mona, Bishakha Uruena, Ana Kollipara, Rahul K Ma, Zhenzhong Borromeo, Mark D Chang, Joshua C Johnson, Jane E |
author_sort | Mona, Bishakha |
collection | PubMed |
description | The mechanisms that activate some genes while silencing others are critical to ensure precision in lineage specification as multipotent progenitors become restricted in cell fate. During neurodevelopment, these mechanisms are required to generate the diversity of neuronal subtypes found in the nervous system. Here we report interactions between basic helix-loop-helix (bHLH) transcriptional activators and the transcriptional repressor PRDM13 that are critical for specifying dorsal spinal cord neurons. PRDM13 inhibits gene expression programs for excitatory neuronal lineages in the dorsal neural tube. Strikingly, PRDM13 also ensures a battery of ventral neural tube specification genes such as Olig1, Olig2 and Prdm12 are excluded dorsally. PRDM13 does this via recruitment to chromatin by multiple neural bHLH factors to restrict gene expression in specific neuronal lineages. Together these findings highlight the function of PRDM13 in repressing the activity of bHLH transcriptional activators that together are required to achieve precise neuronal specification during mouse development. |
format | Online Article Text |
id | pubmed-5576485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55764852017-08-31 Repression by PRDM13 is critical for generating precision in neuronal identity Mona, Bishakha Uruena, Ana Kollipara, Rahul K Ma, Zhenzhong Borromeo, Mark D Chang, Joshua C Johnson, Jane E eLife Developmental Biology The mechanisms that activate some genes while silencing others are critical to ensure precision in lineage specification as multipotent progenitors become restricted in cell fate. During neurodevelopment, these mechanisms are required to generate the diversity of neuronal subtypes found in the nervous system. Here we report interactions between basic helix-loop-helix (bHLH) transcriptional activators and the transcriptional repressor PRDM13 that are critical for specifying dorsal spinal cord neurons. PRDM13 inhibits gene expression programs for excitatory neuronal lineages in the dorsal neural tube. Strikingly, PRDM13 also ensures a battery of ventral neural tube specification genes such as Olig1, Olig2 and Prdm12 are excluded dorsally. PRDM13 does this via recruitment to chromatin by multiple neural bHLH factors to restrict gene expression in specific neuronal lineages. Together these findings highlight the function of PRDM13 in repressing the activity of bHLH transcriptional activators that together are required to achieve precise neuronal specification during mouse development. eLife Sciences Publications, Ltd 2017-08-29 /pmc/articles/PMC5576485/ /pubmed/28850031 http://dx.doi.org/10.7554/eLife.25787 Text en © 2017, Mona 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 | Developmental Biology Mona, Bishakha Uruena, Ana Kollipara, Rahul K Ma, Zhenzhong Borromeo, Mark D Chang, Joshua C Johnson, Jane E Repression by PRDM13 is critical for generating precision in neuronal identity |
title | Repression by PRDM13 is critical for generating precision in neuronal identity |
title_full | Repression by PRDM13 is critical for generating precision in neuronal identity |
title_fullStr | Repression by PRDM13 is critical for generating precision in neuronal identity |
title_full_unstemmed | Repression by PRDM13 is critical for generating precision in neuronal identity |
title_short | Repression by PRDM13 is critical for generating precision in neuronal identity |
title_sort | repression by prdm13 is critical for generating precision in neuronal identity |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576485/ https://www.ncbi.nlm.nih.gov/pubmed/28850031 http://dx.doi.org/10.7554/eLife.25787 |
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