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The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly
Paraspeckles (PS) are nuclear structures scaffolded by the long noncoding RNA NEAT1 and protein components such as NONO and SFPQ. We previously found that the upregulation of RNA N6-methyl-adenosine (m(6)A) demethylase ALKBH5 facilitates hypoxia-induced paraspeckle assembly through erasing m(6)A mar...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Biochemistry and Molecular Biology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457456/ https://www.ncbi.nlm.nih.gov/pubmed/37474102 http://dx.doi.org/10.1016/j.jbc.2023.105071 |
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author | Qin, Xiaoyang Long, Yan Bai, Xue Cao, Lei Yan, Han Zhang, Kai Wang, Bo Wu, Xudong |
author_facet | Qin, Xiaoyang Long, Yan Bai, Xue Cao, Lei Yan, Han Zhang, Kai Wang, Bo Wu, Xudong |
author_sort | Qin, Xiaoyang |
collection | PubMed |
description | Paraspeckles (PS) are nuclear structures scaffolded by the long noncoding RNA NEAT1 and protein components such as NONO and SFPQ. We previously found that the upregulation of RNA N6-methyl-adenosine (m(6)A) demethylase ALKBH5 facilitates hypoxia-induced paraspeckle assembly through erasing m(6)A marks on NEAT1, thus stabilizing it. However, it remains unclear how these processes are spatiotemporally coordinated. Here we discover that ALKBH5 specifically binds to proteins in PS and forms phase-separated droplets that are incorporated into PS through its C-terminal intrinsically disordered region (cIDR). Upon exposure to hypoxia, rapid ALKBH5 condensation in PS induces m(6)A demethylation of NEAT1, which further facilitates PS formation before the upregulation of ALKBH5 expression. In cells expressing ALKBH5 lacking cIDR, PS fail to be formed in response to hypoxia, accompanied with insufficient m(6)A demethylation of NEAT1 and its destabilization. We also demonstrate that ALKBH5-cIDR is indispensable for hypoxia-induced effects such as cancer cell invasion. Therefore, our study has identified the role of ALKBH5 in phase separation as the molecular basis of the positive feedback loop for PS formation between ALKBH5 incorporation into PS and NEAT1 stabilization. |
format | Online Article Text |
id | pubmed-10457456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-104574562023-08-27 The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly Qin, Xiaoyang Long, Yan Bai, Xue Cao, Lei Yan, Han Zhang, Kai Wang, Bo Wu, Xudong J Biol Chem Research Article Paraspeckles (PS) are nuclear structures scaffolded by the long noncoding RNA NEAT1 and protein components such as NONO and SFPQ. We previously found that the upregulation of RNA N6-methyl-adenosine (m(6)A) demethylase ALKBH5 facilitates hypoxia-induced paraspeckle assembly through erasing m(6)A marks on NEAT1, thus stabilizing it. However, it remains unclear how these processes are spatiotemporally coordinated. Here we discover that ALKBH5 specifically binds to proteins in PS and forms phase-separated droplets that are incorporated into PS through its C-terminal intrinsically disordered region (cIDR). Upon exposure to hypoxia, rapid ALKBH5 condensation in PS induces m(6)A demethylation of NEAT1, which further facilitates PS formation before the upregulation of ALKBH5 expression. In cells expressing ALKBH5 lacking cIDR, PS fail to be formed in response to hypoxia, accompanied with insufficient m(6)A demethylation of NEAT1 and its destabilization. We also demonstrate that ALKBH5-cIDR is indispensable for hypoxia-induced effects such as cancer cell invasion. Therefore, our study has identified the role of ALKBH5 in phase separation as the molecular basis of the positive feedback loop for PS formation between ALKBH5 incorporation into PS and NEAT1 stabilization. American Society for Biochemistry and Molecular Biology 2023-07-18 /pmc/articles/PMC10457456/ /pubmed/37474102 http://dx.doi.org/10.1016/j.jbc.2023.105071 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Qin, Xiaoyang Long, Yan Bai, Xue Cao, Lei Yan, Han Zhang, Kai Wang, Bo Wu, Xudong The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly |
title | The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly |
title_full | The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly |
title_fullStr | The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly |
title_full_unstemmed | The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly |
title_short | The disordered C terminus of ALKBH5 promotes phase separation and paraspeckles assembly |
title_sort | disordered c terminus of alkbh5 promotes phase separation and paraspeckles assembly |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457456/ https://www.ncbi.nlm.nih.gov/pubmed/37474102 http://dx.doi.org/10.1016/j.jbc.2023.105071 |
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