Paraspeckle subnuclear bodies depend on dynamic heterodimerisation of DBHS RNA-binding proteins via their structured domains
Details
Publication Year 2022-11,Volume 298,Issue #11,Page 102563
Journal Title
Journal of Biological Chemistry
Publication Type
Research article
Abstract
RNA-binding proteins of the DBHS (Drosophila Behavior Human Splicing) family, NONO, SFPQ, and PSPC1 have numerous roles in genome stability and transcriptional and posttranscriptional regulation. Critical to DBHS activity is their recruitment to distinct subnuclear locations, for example, paraspeckle condensates, where DBHS proteins bind to the long noncoding RNA NEAT1 in the first essential step in paraspeckle formation. To carry out their diverse roles, DBHS proteins form homodimers and heterodimers, but how this dimerization influences DBHS localization and function is unknown. Here, we present an inducible GFP-NONO stable cell line and use it for live-cell 3D-structured illumination microscopy, revealing paraspeckles with dynamic, twisted elongated structures. Using siRNA knockdowns, we show these labeled paraspeckles consist of GFP-NONO/endogenous SFPQ dimers and that GFP-NONO localization to paraspeckles depends on endogenous SFPQ. Using purified proteins, we confirm that partner swapping between NONO and SFPQ occurs readily in vitro. Crystallographic analysis of the NONO-SFPQ heterodimer reveals conformational differences to the other DBHS dimer structures, which may contribute to partner preference, RNA specificity, and subnuclear localization. Thus overall, our study suggests heterodimer partner availability is crucial for NONO subnuclear distribution and helps explain the complexity of both DBHS protein and paraspeckle dynamics through imaging and structural approaches.
Keywords
Humans; Dimerization; *Paraspeckles; RNA-Binding Proteins/metabolism; Gene Expression Regulation; *RNA, Long Noncoding/genetics; Drosophila behavior human splicing (DBHS); Nono; RNA-binding protein; Sfpq; imaging; long noncoding RNA; nuclear organization; paraspeckles; super-resolution microscopy
Department(s)
Laboratory Research
PubMed ID
36209820
Open Access at Publisher's Site
https://doi.org/10.1016/j.jbc.2022.102563
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2025-01-17 02:00:45
Last Modified: 2025-01-17 02:02:19

© 2025 The Walter and Eliza Hall Institute of Medical Research. Access to this website is subject to our Privacy Policy and Terms of Use

An error has occurred. This application may no longer respond until reloaded. Reload 🗙