Authors
Sandra Sinnassamy, Olivia Massiani Beaudoin, Berangère Lombard, Damarys Loew, Tom Bonnifet, Magali Fradet, Héloïse Monnet, Thomas Caille, Nicolas Servant, Rajiv L Joshi, Julia Fuchs
Published in
Life science alliance. Volume 9. Issue 11. Epub Aug 21, 2026.
Abstract
Retrotransposons are emerging as novel regulators of embryonic and brain development. We recently demonstrated that the LINE-1-encoded protein ORF1p is abundantly expressed in adult mouse and human neurons, although its function remains unclear. Here, we characterize the ORF1p interactome in differentiated mouse and human neurons using mass spectrometry and identify novel partners implicated in gene regulation and neuron-specific processes. ORF1p localizes not only to neuronal nuclei, where it associates with chromatin under steady-state conditions, but also to neurites, supporting a role in neuronal physiology. To further explore its nuclear functions, we sorted human post-mortem neurons with high or low nuclear ORF1p levels and performed ORF1p knockdown in cultured human neurons, followed by chromatin accessibility assays. Both approaches revealed consistent patterns of differential chromatin accessibility dependent on ORF1p. Loss of ORF1p also led to the down-regulation of long, neuron-specific genes and altered neurite morphology. Together, these findings point to a physiological role of ORF1p in post-mitotic neurons, mediated through converging interactions with proteins and chromatin.
PMID:
42629196
Bibliographic data and abstract were imported from PubMed on 22 Aug 2026.
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