The lincRNA Pantr1 is a FOXG1 target gene conferring site-specific chromatin binding of FOXG1
Fabian GatheriD, Tudor RauleaciD, Ipek AkoliD, Ganeshkumar Arumugam, Camila L. FullioiD, Teresa MülleriD, Dimitrios KleidonasiD, André FischeriD, Andreas VlachosiD, Rolf BackofeniD, Tanja VogeliD
Abstract
Derailed gene expression programs within the developing nervous system, encompassing both transcriptional and posttranscriptional processes, can cause diverse neurodevelopmental diseases (NDD). The NDD FOXG1-syndrome lacks full understanding of the mechanistic role of its eponymous gene product. While it is known that FOXG1 acts in part at the chromatin by binding to regulative regions, it is unclear what factors control its presence at specific sites. Long non-coding RNAs (lncRNAs) can mediate site-directed transcription factor binding, but their potential role in FOXG1-syndrome has not been described. Here, we show that FOXG1 localisation is regulated at selected loci through the lncRNA Pantr1. We identified FOXG1 as an upstream transcriptional activator of Pantr1 in human and mice. Further, we discovered that FOXG1 has the ability to associate with RNAs. Both, transcriptional regulation of Pantr1 by FOXG1 and association of both partners, build up a regulative network that impacts the localisation of FOXG1 at selected genomic loci. Specifically, Pantr1 facilitates cooperative presence of FOXG1/NEUROD1 at specific sites, and Pantr1 reduction leads to redistribution of FOXG1 to comparably more generic binding sites. The rescue of impaired dendritic outgrowth upon FOXG1 reduction by simultaneous overexpression of Pantr1 underlines the importance of the FOXG1/Pantr1 regulative network. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=79 SRC="FIGDIR/small/610239v1_ufig1.gif" ALT="Figure 1"> View larger version (23K): org.highwire.dtl.DTLVardef@19ecb05org.highwire.dtl.DTLVardef@22cfbcorg.highwire.dtl.DTLVardef@1748056org.highwire.dtl.DTLVardef@1959e3c_HPS_FORMAT_FIGEXP M_FIG C_FIG
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Foxg1 bimodally tunes L1-mRNA and -DNA dynamics in the developing murine neocortex
Gabriele Liuzzi, Osvaldo Artimagnella, … Antonello Mallamaci·DevelopmentPeer-reviewed·Apr 24, 2024
- Non-coding structural variants identify a commonly affected regulatory region steering FOXG1 transcription in early neurodevelopment
Lisa Hamerlinck, Eva D’haene, … Sarah Vergult·medRxiv·Mar 10, 2025
- Integrative multi-omics analyses reveal multi-modal FOXG1 functions acting on epigenetic processes and in concert with NEUROD1 to regulate synaptogenesis in the mouse hippocampus
Ipek Akol, Annalisa Izzo, … Tanja Vogel·Proceedings of the National Academy of SciencesPeer-reviewed·Jan 4, 2023
- Analysis of 14q12 microdeletions reveals novel regulatory loci for the neurodevelopmental disorder-related gene, FOXG1
Aishwarya Ramamurthy, Masha D Bandouil, … Gemma L. Carvill·Nature CommunicationsPeer-reviewed·Jul 21, 2026
- The lncRNA FENDRR fine-tunes FOXF1 protein levels through a negative feedback loop governing human embryonic lung fibroblast-to-myofibroblast transition
Jean-Francois Laurendeau, Sophie Mockly, … Martin Sauvageau·bioRxiv·Apr 12, 2026
- The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders
Cheen Euong Ang, Qing Ma, … Howard Y. Chang·eLifePeer-reviewed·Jan 10, 2019