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A meiosis-specific Spt5 homolog involved in non-coding transcription
Spt5 is a conserved and essential transcriptional regulator that binds directly to RNA polymerase and is involved in transcription elongation, polymerase pausing and various co-transcriptional processes. To investigate the role of Spt5 in non-coding transcription, we used the unicellular model Param...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416832/ https://www.ncbi.nlm.nih.gov/pubmed/28053118 http://dx.doi.org/10.1093/nar/gkw1318 |
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author | Gruchota, Julita Denby Wilkes, Cyril Arnaiz, Olivier Sperling, Linda Nowak, Jacek K. |
author_facet | Gruchota, Julita Denby Wilkes, Cyril Arnaiz, Olivier Sperling, Linda Nowak, Jacek K. |
author_sort | Gruchota, Julita |
collection | PubMed |
description | Spt5 is a conserved and essential transcriptional regulator that binds directly to RNA polymerase and is involved in transcription elongation, polymerase pausing and various co-transcriptional processes. To investigate the role of Spt5 in non-coding transcription, we used the unicellular model Paramecium tetraurelia. In this ciliate, development is controlled by epigenetic mechanisms that use different classes of non-coding RNAs to target DNA elimination. We identified two SPT5 genes. One (STP5v) is involved in vegetative growth, while the other (SPT5m) is essential for sexual reproduction. We focused our study on SPT5m, expressed at meiosis and associated with germline nuclei during sexual processes. Upon Spt5m depletion, we observed absence of scnRNAs, piRNA-like 25 nt small RNAs produced at meiosis. The scnRNAs are a temporal copy of the germline genome and play a key role in programming DNA elimination. Moreover, Spt5m depletion abolishes elimination of all germline-limited sequences, including sequences whose excision was previously shown to be scnRNA-independent. This suggests that in addition to scnRNA production, Spt5 is involved in setting some as yet uncharacterized epigenetic information at meiosis. Our study establishes that Spt5m is crucial for developmental genome rearrangements and necessary for scnRNA production. |
format | Online Article Text |
id | pubmed-5416832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54168322017-05-05 A meiosis-specific Spt5 homolog involved in non-coding transcription Gruchota, Julita Denby Wilkes, Cyril Arnaiz, Olivier Sperling, Linda Nowak, Jacek K. Nucleic Acids Res RNA Spt5 is a conserved and essential transcriptional regulator that binds directly to RNA polymerase and is involved in transcription elongation, polymerase pausing and various co-transcriptional processes. To investigate the role of Spt5 in non-coding transcription, we used the unicellular model Paramecium tetraurelia. In this ciliate, development is controlled by epigenetic mechanisms that use different classes of non-coding RNAs to target DNA elimination. We identified two SPT5 genes. One (STP5v) is involved in vegetative growth, while the other (SPT5m) is essential for sexual reproduction. We focused our study on SPT5m, expressed at meiosis and associated with germline nuclei during sexual processes. Upon Spt5m depletion, we observed absence of scnRNAs, piRNA-like 25 nt small RNAs produced at meiosis. The scnRNAs are a temporal copy of the germline genome and play a key role in programming DNA elimination. Moreover, Spt5m depletion abolishes elimination of all germline-limited sequences, including sequences whose excision was previously shown to be scnRNA-independent. This suggests that in addition to scnRNA production, Spt5 is involved in setting some as yet uncharacterized epigenetic information at meiosis. Our study establishes that Spt5m is crucial for developmental genome rearrangements and necessary for scnRNA production. Oxford University Press 2017-05-05 2017-01-02 /pmc/articles/PMC5416832/ /pubmed/28053118 http://dx.doi.org/10.1093/nar/gkw1318 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | RNA Gruchota, Julita Denby Wilkes, Cyril Arnaiz, Olivier Sperling, Linda Nowak, Jacek K. A meiosis-specific Spt5 homolog involved in non-coding transcription |
title | A meiosis-specific Spt5 homolog involved in non-coding transcription |
title_full | A meiosis-specific Spt5 homolog involved in non-coding transcription |
title_fullStr | A meiosis-specific Spt5 homolog involved in non-coding transcription |
title_full_unstemmed | A meiosis-specific Spt5 homolog involved in non-coding transcription |
title_short | A meiosis-specific Spt5 homolog involved in non-coding transcription |
title_sort | meiosis-specific spt5 homolog involved in non-coding transcription |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416832/ https://www.ncbi.nlm.nih.gov/pubmed/28053118 http://dx.doi.org/10.1093/nar/gkw1318 |
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