Subcellular depletion of importin β1 impairs presynaptic local translation and spatial memory

Axonal localization and local translation of mRNA encoding importin β1 are important for retrograde injury signaling and axonal growth. Here, we found that loss of importin β1 in axons through deletion of the mRNA's 3' untranslated region (3'UTR) caused a specific spatial memory deficit in mice. Electrophysiological analyses of hippocampal circuits revealed that mice expressing importin β1 transcripts lacking the 3'UTR (∆3'UTR) had impaired long-term potentiation (LTP) in presynaptic mossy fibers. Furthermore, mass spectrometry revealed an altered synaptic proteome and phosphoproteome, and sequencing of ribosome-associated RNAs showed suppression of locally translated presynaptic mRNAs in dentate gyrus neurons from mice expressing ∆3'UTR importin β1. This dysregulation was reflected in a reduction in the readily releasable pool of synaptic vesicles in mossy fiber synapses. Thus, axonal localization of importin β1-encoding mRNA is required to shape the presynapse, and disruption of this mechanism causes memory deficits.

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Journal
Science Signaling
Published
2026-01-20
DOI
https://doi.org/10.1126/scisignal.ady2026
Primary Topic
Nuclear Structure and Function
Type
article
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article

Subcellular depletion of importin β1 impairs presynaptic local translation and spatial memory

Ida Rishal, Nicolas Panayotis, Michael Tsoory, Michaela Schweizer et al.
Science Signaling
Nuclear Structure and Function
article

Subcellular depletion of importin β1 impairs presynaptic local translation and spatial memory

Ida Rishal, Nicolas Panayotis, Michael Tsoory, Michaela Schweizer, Anna Karpova, Katarzyna M. Grochowska, Leilah Krounbi, Philip A. Freund, Sebastian Samer, RIKI KAWAGUCHI, Juan A. Osés-Prieto, PingAn Yuanxiang, Talieh Zomorrodinia, Mike Fainzilber, Michael R. Kreutz, Alma L. Burlingame
article en

Abstract

Axonal localization and local translation of mRNA encoding importin β1 are important for retrograde injury signaling and axonal growth. Here, we found that loss of importin β1 in axons through deletion of the mRNA's 3' untranslated region (3'UTR) caused a specific spatial memory deficit in mice. Electrophysiological analyses of hippocampal circuits revealed that mice expressing importin β1 transcripts lacking the 3'UTR (∆3'UTR) had impaired long-term potentiation (LTP) in presynaptic mossy fibers. Furthermore, mass spectrometry revealed an altered synaptic proteome and phosphoproteome, and sequencing of ribosome-associated RNAs showed suppression of locally translated presynaptic mRNAs in dentate gyrus neurons from mice expressing ∆3'UTR importin β1. This dysregulation was reflected in a reduction in the readily releasable pool of synaptic vesicles in mossy fiber synapses. Thus, axonal localization of importin β1-encoding mRNA is required to shape the presynapse, and disruption of this mechanism causes memory deficits.

Science SignalingVol. 19(921)
Centre National de la Recherche Scientifique (FR), Universität Hamburg (DE), University of California, Los Angeles (US), University of California, San Francisco (US), Université Paris Cité (FR), University Medical Center Hamburg-Eppendorf (DE), Institut de Psychiatrie et Neurosciences de Paris (FR), SPPIN - Saints-Pères Paris Institute for Neurosciences (FR), Weizmann Institute of Science (IL), Leibniz Institute for Neurobiology (DE)
Openalex Percentile: Top 84%
Nuclear Structure and Function
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