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Transcriptional interference by antisense RNA is required for circadian clock function
Eukaryotic circadian oscillators consist of negative feedback loops that generate endogenous rhythmicities(1). Natural antisense RNAs are found in a wide range of eukaryotic organisms(2-5). Nevertheless, the physiological importance and mode of action of most antisense RNAs is not clear(6-9). freque...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214883/ https://www.ncbi.nlm.nih.gov/pubmed/25132551 http://dx.doi.org/10.1038/nature13671 |
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author | Xue, Zhihong Ye, Qiaohong Anson, Simon R Yang, Jichen Xiao, Guanghua Kowbel, David Glass, N. Louise Crosthwaite, Susan K. Liu, Yi |
author_facet | Xue, Zhihong Ye, Qiaohong Anson, Simon R Yang, Jichen Xiao, Guanghua Kowbel, David Glass, N. Louise Crosthwaite, Susan K. Liu, Yi |
author_sort | Xue, Zhihong |
collection | PubMed |
description | Eukaryotic circadian oscillators consist of negative feedback loops that generate endogenous rhythmicities(1). Natural antisense RNAs are found in a wide range of eukaryotic organisms(2-5). Nevertheless, the physiological importance and mode of action of most antisense RNAs is not clear(6-9). frequency (frq) encodes a component of the Neurospora core circadian negative feedback loop which was thought to generate sustained rhythmicity(10). Transcription of qrf, the long non-coding frq antisense RNA, is light induced, and its level oscillates in antiphase to frq sense RNA(3). Here we show that qrf transcription is regulated by both light-dependent and -independent mechanisms. Light-dependent qrf transcription represses frq expression and regulates clock resetting. qrf expression in the dark, on the other hand, is required for circadian rhythmicity. frq transcription also inhibits qrf expression and surprisingly, drives the antiphasic rhythm of qrf transcripts. The mutual inhibition of frq and qrf transcription thus forms a double negative feedback loop that is interlocked with the core feedback loop. Genetic and mathematical modeling analyses indicate that such an arrangement is required for robust and sustained circadian rhythmicity. Moreover, our results suggest that antisense transcription inhibits sense expression by mediating chromatin modifications and premature transcription termination. Together, our results established antisense transcription as an essential feature in a circadian system and shed light on the importance and mechanism of antisense action. |
format | Online Article Text |
id | pubmed-4214883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42148832015-04-30 Transcriptional interference by antisense RNA is required for circadian clock function Xue, Zhihong Ye, Qiaohong Anson, Simon R Yang, Jichen Xiao, Guanghua Kowbel, David Glass, N. Louise Crosthwaite, Susan K. Liu, Yi Nature Article Eukaryotic circadian oscillators consist of negative feedback loops that generate endogenous rhythmicities(1). Natural antisense RNAs are found in a wide range of eukaryotic organisms(2-5). Nevertheless, the physiological importance and mode of action of most antisense RNAs is not clear(6-9). frequency (frq) encodes a component of the Neurospora core circadian negative feedback loop which was thought to generate sustained rhythmicity(10). Transcription of qrf, the long non-coding frq antisense RNA, is light induced, and its level oscillates in antiphase to frq sense RNA(3). Here we show that qrf transcription is regulated by both light-dependent and -independent mechanisms. Light-dependent qrf transcription represses frq expression and regulates clock resetting. qrf expression in the dark, on the other hand, is required for circadian rhythmicity. frq transcription also inhibits qrf expression and surprisingly, drives the antiphasic rhythm of qrf transcripts. The mutual inhibition of frq and qrf transcription thus forms a double negative feedback loop that is interlocked with the core feedback loop. Genetic and mathematical modeling analyses indicate that such an arrangement is required for robust and sustained circadian rhythmicity. Moreover, our results suggest that antisense transcription inhibits sense expression by mediating chromatin modifications and premature transcription termination. Together, our results established antisense transcription as an essential feature in a circadian system and shed light on the importance and mechanism of antisense action. 2014-08-17 2014-10-30 /pmc/articles/PMC4214883/ /pubmed/25132551 http://dx.doi.org/10.1038/nature13671 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Xue, Zhihong Ye, Qiaohong Anson, Simon R Yang, Jichen Xiao, Guanghua Kowbel, David Glass, N. Louise Crosthwaite, Susan K. Liu, Yi Transcriptional interference by antisense RNA is required for circadian clock function |
title | Transcriptional interference by antisense RNA is required for circadian clock function |
title_full | Transcriptional interference by antisense RNA is required for circadian clock function |
title_fullStr | Transcriptional interference by antisense RNA is required for circadian clock function |
title_full_unstemmed | Transcriptional interference by antisense RNA is required for circadian clock function |
title_short | Transcriptional interference by antisense RNA is required for circadian clock function |
title_sort | transcriptional interference by antisense rna is required for circadian clock function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214883/ https://www.ncbi.nlm.nih.gov/pubmed/25132551 http://dx.doi.org/10.1038/nature13671 |
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