Cargando…
Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis
Recent studies implicate Poly (ADP-ribose) polymerase 1 (PARP1) in alternative splicing regulation, and PARP1 may be an RNA-binding protein. However, detailed knowledge of RNA targets and the RNA-binding region for PARP1 are unknown. Here we report the first global study of PARP1–RNA interactions us...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787697/ https://www.ncbi.nlm.nih.gov/pubmed/29387452 http://dx.doi.org/10.1038/celldisc.2017.43 |
_version_ | 1783295985267507200 |
---|---|
author | Melikishvili, Manana Chariker, Julia H Rouchka, Eric C Fondufe-Mittendorf, Yvonne N |
author_facet | Melikishvili, Manana Chariker, Julia H Rouchka, Eric C Fondufe-Mittendorf, Yvonne N |
author_sort | Melikishvili, Manana |
collection | PubMed |
description | Recent studies implicate Poly (ADP-ribose) polymerase 1 (PARP1) in alternative splicing regulation, and PARP1 may be an RNA-binding protein. However, detailed knowledge of RNA targets and the RNA-binding region for PARP1 are unknown. Here we report the first global study of PARP1–RNA interactions using PAR–CLIP in HeLa cells. We identified a largely overlapping set of 22 142 PARP1–RNA-binding peaks mapping to mRNAs, with 20 484 sites located in intronic regions. PARP1 preferentially bound RNA containing GC-rich sequences. Using a Bayesian model, we determined positional effects of PARP1 on regulated exon-skipping events: PARP1 binding upstream and downstream of the skipped exons generally promotes exon inclusion, whereas binding within the exon of interest and intronic regions closer to the skipped exon promotes exon skipping. Using truncation mutants, we show that removal of the Zn1Zn2 domain switches PARP1 from a DNA binder to an RNA binder. This study represents a first step into understanding the role of PARP1–RNA interaction. Continued identification and characterization of the functional interplay between PARPs and RNA may provide important insights into the role of PARPs in RNA regulation. |
format | Online Article Text |
id | pubmed-5787697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57876972018-01-31 Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis Melikishvili, Manana Chariker, Julia H Rouchka, Eric C Fondufe-Mittendorf, Yvonne N Cell Discov Article Recent studies implicate Poly (ADP-ribose) polymerase 1 (PARP1) in alternative splicing regulation, and PARP1 may be an RNA-binding protein. However, detailed knowledge of RNA targets and the RNA-binding region for PARP1 are unknown. Here we report the first global study of PARP1–RNA interactions using PAR–CLIP in HeLa cells. We identified a largely overlapping set of 22 142 PARP1–RNA-binding peaks mapping to mRNAs, with 20 484 sites located in intronic regions. PARP1 preferentially bound RNA containing GC-rich sequences. Using a Bayesian model, we determined positional effects of PARP1 on regulated exon-skipping events: PARP1 binding upstream and downstream of the skipped exons generally promotes exon inclusion, whereas binding within the exon of interest and intronic regions closer to the skipped exon promotes exon skipping. Using truncation mutants, we show that removal of the Zn1Zn2 domain switches PARP1 from a DNA binder to an RNA binder. This study represents a first step into understanding the role of PARP1–RNA interaction. Continued identification and characterization of the functional interplay between PARPs and RNA may provide important insights into the role of PARPs in RNA regulation. Nature Publishing Group 2017-11-28 /pmc/articles/PMC5787697/ /pubmed/29387452 http://dx.doi.org/10.1038/celldisc.2017.43 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Melikishvili, Manana Chariker, Julia H Rouchka, Eric C Fondufe-Mittendorf, Yvonne N Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis |
title | Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis |
title_full | Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis |
title_fullStr | Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis |
title_full_unstemmed | Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis |
title_short | Transcriptome-wide identification of the RNA-binding landscape of the chromatin-associated protein PARP1 reveals functions in RNA biogenesis |
title_sort | transcriptome-wide identification of the rna-binding landscape of the chromatin-associated protein parp1 reveals functions in rna biogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787697/ https://www.ncbi.nlm.nih.gov/pubmed/29387452 http://dx.doi.org/10.1038/celldisc.2017.43 |
work_keys_str_mv | AT melikishvilimanana transcriptomewideidentificationofthernabindinglandscapeofthechromatinassociatedproteinparp1revealsfunctionsinrnabiogenesis AT charikerjuliah transcriptomewideidentificationofthernabindinglandscapeofthechromatinassociatedproteinparp1revealsfunctionsinrnabiogenesis AT rouchkaericc transcriptomewideidentificationofthernabindinglandscapeofthechromatinassociatedproteinparp1revealsfunctionsinrnabiogenesis AT fondufemittendorfyvonnen transcriptomewideidentificationofthernabindinglandscapeofthechromatinassociatedproteinparp1revealsfunctionsinrnabiogenesis |