Transcription levels of a long noncoding RNA orchestrate opposing regulatory and cell fate outcomes in yeast
ABSTRACT Many long noncoding RNAs (lncRNAs) act in cis through transcription-coupled chromatin alterations that drive changes in local gene expression. How some cis-acting lncRNAs promote and others repress gene expression remains poorly understood. Here we report that in S. cerevisiae transcription levels of the lncRNA IRT2, located upstream in the promoter of the inducer of meiosis gene, regulate opposing chromatin and transcription states. Low IRT2 transcription displays enhancer RNA-like features. At these levels, IRT2 promotes histone exchange delivering acetylated histone H3 lysine 56 to chromatin thereby facilitating recruitment of a transcription factor and consequently activating transcription. Conversely, increasing IRT2 transcription enhances chromatin assembly and transcriptional repression. The opposing functions of IRT2 direct a regulatory circuit, which ensures that cells expressing opposite, but not one of either, mating-type loci enter meiosis. Our data demonstrate that the transcription levels of an lncRNA are key to controlling gene expression and cell fate outcomes..
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Preprint| Erscheinungsjahr: |
2021 |
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| Erschienen: |
2021 |
| Enthalten in: |
bioRxiv.org - (2021) vom: 15. Dez. Zur Gesamtaufnahme - year:2021 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Moretto, Fabien [VerfasserIn] |
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| doi: |
10.1101/2019.12.24.887935 |
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| PPN (Katalog-ID): |
XBI000688320 |
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| 245 | 1 | 0 | |a Transcription levels of a long noncoding RNA orchestrate opposing regulatory and cell fate outcomes in yeast |
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| 520 | |a ABSTRACT Many long noncoding RNAs (lncRNAs) act in cis through transcription-coupled chromatin alterations that drive changes in local gene expression. How some cis-acting lncRNAs promote and others repress gene expression remains poorly understood. Here we report that in S. cerevisiae transcription levels of the lncRNA IRT2, located upstream in the promoter of the inducer of meiosis gene, regulate opposing chromatin and transcription states. Low IRT2 transcription displays enhancer RNA-like features. At these levels, IRT2 promotes histone exchange delivering acetylated histone H3 lysine 56 to chromatin thereby facilitating recruitment of a transcription factor and consequently activating transcription. Conversely, increasing IRT2 transcription enhances chromatin assembly and transcriptional repression. The opposing functions of IRT2 direct a regulatory circuit, which ensures that cells expressing opposite, but not one of either, mating-type loci enter meiosis. Our data demonstrate that the transcription levels of an lncRNA are key to controlling gene expression and cell fate outcomes. | ||
| 700 | 1 | |a Wood, N. Ezgi |e verfasserin |4 aut | |
| 700 | 1 | |a Chia, Minghao |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Cai |e verfasserin |4 aut | |
| 700 | 1 | |a Luscombe, Nicholas M. |e verfasserin |4 aut | |
| 700 | 1 | |a van Werven, Folkert J. |e verfasserin |4 aut | |
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