ARC/ARG3.1 binds the nuclear polyadenylate-binding protein RRM and regulates neuronal activity-dependent formation of nuclear speckles

ARC is a neuronal activity-induced protein interaction hub with critical roles in synaptic plasticity and memory. ARC localizes to synapses and the nucleus, but its nuclear functions are little known. Following in vivo long-term potentiation (LTP) induction in the dentate gyrus, we show that ARC accumulates in the nucleosol fraction and interchromatin space of granule cells. Proteomic analysis of immunoprecipitated ARC complexes identifies proteins involved in pre-mRNA processing. We demonstrate endogenous ARC protein-protein interaction with polyadenylate-binding nuclear protein 1 (PABPN1) and the paraspeckles protein polypyrimidine tract-binding protein (PTB)-associated splicing factor (PSF). In vitro peptide binding arrays show direct binding of purified ARC to the PABPN1 poly(A)-RNA recognition motif. 3D morphometric imaging reveals structural changes in PABPN1 foci corresponding to classical nuclear speckles following in vivo and in vitro LTP. Depletion of ARC disrupts the maintenance and activity-dependent formation of PABPN1 speckles, thus implicating ARC in regulation of nuclear speckle dynamics and pre-mRNA processing.

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Publication Details

Journal
Cell Reports
Published
2025-04-01
DOI
https://doi.org/10.1016/j.celrep.2025.115525
Citations
1
Primary Topic
Nuclear Structure and Function
Type
article
Field-Weighted Citation Impact
0.81
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article

ARC/ARG3.1 binds the nuclear polyadenylate-binding protein RRM and regulates neuronal activity-dependent formation of nuclear speckles

Tambudzai Kanhema, Sudarshan Patil, Petri Kursula, Kamil Parobczak et al.
1 citations
Cell Reports
Nuclear Structure and Function
0.81
article

ARC/ARG3.1 binds the nuclear polyadenylate-binding protein RRM and regulates neuronal activity-dependent formation of nuclear speckles

Tambudzai Kanhema, Sudarshan Patil, Petri Kursula, Kamil Parobczak, Abdulla Mahboob, Erik I. Hallin, Clive R. Bramham, Adriana Magalska, François Philippe Pauzin, Adrian Szum, Grzegorz M. Wilczyński, Jan Ludwiczak, Stanisław Dunin-Horkawicz, Andrzej A. Szczepankiewicz, Dagmara Holm-Kaczmarek, Yuta Ishizuka
article en
1 citations

Abstract

ARC is a neuronal activity-induced protein interaction hub with critical roles in synaptic plasticity and memory. ARC localizes to synapses and the nucleus, but its nuclear functions are little known. Following in vivo long-term potentiation (LTP) induction in the dentate gyrus, we show that ARC accumulates in the nucleosol fraction and interchromatin space of granule cells. Proteomic analysis of immunoprecipitated ARC complexes identifies proteins involved in pre-mRNA processing. We demonstrate endogenous ARC protein-protein interaction with polyadenylate-binding nuclear protein 1 (PABPN1) and the paraspeckles protein polypyrimidine tract-binding protein (PTB)-associated splicing factor (PSF). In vitro peptide binding arrays show direct binding of purified ARC to the PABPN1 poly(A)-RNA recognition motif. 3D morphometric imaging reveals structural changes in PABPN1 foci corresponding to classical nuclear speckles following in vivo and in vitro LTP. Depletion of ARC disrupts the maintenance and activity-dependent formation of PABPN1 speckles, thus implicating ARC in regulation of nuclear speckle dynamics and pre-mRNA processing.

Cell ReportsVol. 44(4)
Roche (Switzerland) (CH), Max Planck Institute for Developmental Biology (DE), Max Planck Institute for Biology (DE), University of Bergen (NO), Polish Academy of Sciences (PL)
Openalex Percentile: Top 29%
Nuclear Structure and Function
0.81
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