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RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis

SPT6 is a conserved elongation factor that is associated with phosphorylated RNA polymerase II (RNAPII) during transcription. Recent transcriptome analysis in yeast mutants revealed its potential role in the control of transcription initiation at genic promoters. However, the mechanism by which this...

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Autores principales: Chen, Chen, Shu, Jie, Li, Chenlong, Thapa, Raj K, Nguyen, Vi, Yu, Kangfu, Yuan, Ze-Chun, Kohalmi, Susanne E, Liu, Jun, Marsolais, Frédéric, Huang, Shangzhi, Cui, Yuhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648355/
https://www.ncbi.nlm.nih.gov/pubmed/31127286
http://dx.doi.org/10.1093/nar/gkz465
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author Chen, Chen
Shu, Jie
Li, Chenlong
Thapa, Raj K
Nguyen, Vi
Yu, Kangfu
Yuan, Ze-Chun
Kohalmi, Susanne E
Liu, Jun
Marsolais, Frédéric
Huang, Shangzhi
Cui, Yuhai
author_facet Chen, Chen
Shu, Jie
Li, Chenlong
Thapa, Raj K
Nguyen, Vi
Yu, Kangfu
Yuan, Ze-Chun
Kohalmi, Susanne E
Liu, Jun
Marsolais, Frédéric
Huang, Shangzhi
Cui, Yuhai
author_sort Chen, Chen
collection PubMed
description SPT6 is a conserved elongation factor that is associated with phosphorylated RNA polymerase II (RNAPII) during transcription. Recent transcriptome analysis in yeast mutants revealed its potential role in the control of transcription initiation at genic promoters. However, the mechanism by which this is achieved and how this is linked to elongation remains to be elucidated. Here, we present the genome-wide occupancy of Arabidopsis SPT6-like (SPT6L) and demonstrate its conserved role in facilitating RNAPII occupancy across transcribed genes. We also further demonstrate that SPT6L enrichment is unexpectedly shifted, from gene body to transcription start site (TSS), when its association with RNAPII is disrupted. Protein domains, required for proper function and enrichment of SPT6L on chromatin, are subsequently identified. Finally, our results suggest that recruitment of SPT6L at TSS is indispensable for its spreading along the gene body during transcription. These findings provide new insights into the mechanisms underlying SPT6L recruitment in transcription and shed light on the coordination between transcription initiation and elongation.
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spelling pubmed-66483552019-07-29 RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis Chen, Chen Shu, Jie Li, Chenlong Thapa, Raj K Nguyen, Vi Yu, Kangfu Yuan, Ze-Chun Kohalmi, Susanne E Liu, Jun Marsolais, Frédéric Huang, Shangzhi Cui, Yuhai Nucleic Acids Res Gene regulation, Chromatin and Epigenetics SPT6 is a conserved elongation factor that is associated with phosphorylated RNA polymerase II (RNAPII) during transcription. Recent transcriptome analysis in yeast mutants revealed its potential role in the control of transcription initiation at genic promoters. However, the mechanism by which this is achieved and how this is linked to elongation remains to be elucidated. Here, we present the genome-wide occupancy of Arabidopsis SPT6-like (SPT6L) and demonstrate its conserved role in facilitating RNAPII occupancy across transcribed genes. We also further demonstrate that SPT6L enrichment is unexpectedly shifted, from gene body to transcription start site (TSS), when its association with RNAPII is disrupted. Protein domains, required for proper function and enrichment of SPT6L on chromatin, are subsequently identified. Finally, our results suggest that recruitment of SPT6L at TSS is indispensable for its spreading along the gene body during transcription. These findings provide new insights into the mechanisms underlying SPT6L recruitment in transcription and shed light on the coordination between transcription initiation and elongation. Oxford University Press 2019-07-26 2019-05-25 /pmc/articles/PMC6648355/ /pubmed/31127286 http://dx.doi.org/10.1093/nar/gkz465 Text en © The Author(s) 2019. 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 Non-Commercial 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 Gene regulation, Chromatin and Epigenetics
Chen, Chen
Shu, Jie
Li, Chenlong
Thapa, Raj K
Nguyen, Vi
Yu, Kangfu
Yuan, Ze-Chun
Kohalmi, Susanne E
Liu, Jun
Marsolais, Frédéric
Huang, Shangzhi
Cui, Yuhai
RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis
title RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis
title_full RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis
title_fullStr RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis
title_full_unstemmed RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis
title_short RNA polymerase II-independent recruitment of SPT6L at transcription start sites in Arabidopsis
title_sort rna polymerase ii-independent recruitment of spt6l at transcription start sites in arabidopsis
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648355/
https://www.ncbi.nlm.nih.gov/pubmed/31127286
http://dx.doi.org/10.1093/nar/gkz465
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