# Reorganization of the heterochromatin-associated gene-dense subcompartment in early neuronal development

**Authors:** Nicolas J. Scrutton Alvarado, Ziyu Zhao, Tomoko Yamada, Yue Yang

PMC · DOI: 10.1242/bio.062005 · 2025-05-12

## TL;DR

This study shows that specific parts of the genome reorganize during early brain cell development, moving closer to the nucleus and forming stronger connections.

## Contribution

The paper identifies the specific developmental stage when gene-dense regions reorganize in neurons and their association with heterochromatin.

## Key findings

- hGD regions relocalize toward the nuclear interior during granule neuron differentiation.
- hGD regions strengthen chromosomal interactions while remaining distinct from other nuclear bodies.
- These changes occur independently of transcriptional changes during differentiation.

## Abstract

The 3D organization of the genome has emerged as an important regulator of cellular development. Post-mitotic neurons undergo conserved changes in genome organization, such as the inward radial repositioning of heterochromatin-rich chromosomes as they differentiate. Additionally, transcriptionally active but heterochromatin-associated gene-dense (hGD) regions significantly strengthen their long-distance interactions during cerebellar development. However, the specific developmental stages during which these nuclear changes take place have remained poorly defined. Here, we report that hGD regions relocalize toward the nuclear interior and strengthen their chromosomal interactions as immature granule neurons transition from active cell migration to subsequent stages of neuronal differentiation. During this period, hGD genomic regions are coordinately repositioned in the nucleus alongside their physically tethered heterochromatic chromocenters. Despite these major changes in nuclear organization, the hGD subcompartment remains distinct from other transcriptionally active or repressive nuclear bodies, including heterochromatic chromocenters, throughout development. Notably, these nuclear changes appear to be independent of transcriptional changes that occur during granule neuron differentiation. Together, our results provide insights into the developmental timing of structural changes in the chromosomes of post-mitotic neurons.

Summary: Chromosomal reorganization of a transcriptionally active gene-dense subcompartment tethered to heterochromatic chromocenters occurs during early granule neuron development in the cerebellum.

## Full-text entities

- **Genes:** Rbfox3 (RNA binding protein, fox-1 homolog (C. elegans) 3) [NCBI Gene 52897] {aka Fox-3, Hrnbp3, NeuN, Neuna60}, Top2b (topoisomerase (DNA) II beta) [NCBI Gene 21974] {aka D230016L12Rik, Top-2}, Chd4 (chromodomain helicase DNA binding protein 4) [NCBI Gene 107932] {aka 9530019N15Rik, D6Ertd380e, Mi-2beta, mKIAA4075}, H3c7 (H3 clustered histone 7) [NCBI Gene 260423] {aka H3.2-221, H3c13, H3c14, H3c15, H3c2, H3c3}, Nucleolin (nucleolin multifunctional protein) [NCBI Gene 17975] {aka B530004O11Rik, C23, D0Nds28, D1Nds28, Ncl, Nucl}, Grin2c (glutamate receptor, ionotropic, NMDA2C (epsilon 3)) [NCBI Gene 14813] {aka GluN2C, NMDAR2C, NR2C}, Pax6 (paired box 6) [NCBI Gene 18508] {aka 1500038E17Rik, AEY11, Dey, Gsfaey11, Pax-6, Sey}, Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345] {aka D630048A14Rik, Ki-67, Ki67}, Kptn (kaptin) [NCBI Gene 70394] {aka 2310042D10Rik, 2E4, C030013F01Rik}, Sf3a2 (splicing factor 3a, subunit 2) [NCBI Gene 20222] {aka 66kDa, PRP11, SFA66, Sap62}, Nebl (nebulette) [NCBI Gene 74103] {aka 1200007O21Rik, A630080F05Rik, D830029A09Rik, Lnebl}, Dcx (doublecortin) [NCBI Gene 13193] {aka Dbct}, Rmdn2 (regulator of microtubule dynamics 2) [NCBI Gene 381110] {aka Fam82a1, RMD-2, mRMD-2}, Igl (immunoglobulin lambda chain complex) [NCBI Gene 111519] {aka Igl-x}, Zmat4 (zinc finger, matrin type 4) [NCBI Gene 320158] {aka 9630048M01Rik}, Chd7 (chromodomain helicase DNA binding protein 7) [NCBI Gene 320790] {aka A730019I05Rik, Cycn, Cyn, Dz, Edy, Flo}, Ivns1abp (influenza virus NS1A binding protein) [NCBI Gene 117198] {aka 1190004M08Rik, 1700126I16Rik, HSPC068, ND1, NS-1, NS1-BP}, Hgd (homogentisate 1, 2-dioxygenase) [NCBI Gene 15233] {aka Hgo, aku}
- **Diseases:** FANS (MESH:C566014)
- **Chemicals:** Triton-X (MESH:D017830), PBS (MESH:D007854), Alexa 647 (MESH:C569686), dextran sulfate (MESH:D016264), sucrose (MESH:D013395), SDS (MESH:D012967), glycine (MESH:D005998), sodium citrate (MESH:D000077559), Hoechst 33342 (MESH:C017807), 1xPBS (-), HCl (MESH:D006851), NaCl (MESH:D012965), EDTA (MESH:D004492), PMC (MESH:C008859), formamide (MESH:C031066), EtOH (MESH:D000431)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12091228/full.md

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Source: https://tomesphere.com/paper/PMC12091228