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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...

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Autores principales: Qin, Xiaoyang, Long, Yan, Bai, Xue, Cao, Lei, Yan, Han, Zhang, Kai, Wang, Bo, Wu, Xudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
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.
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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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