Evidence map›Paper›PMID 37676945›Full record

ArticleScience (New York, N.Y.)2023

Lifelong restructuring of 3D genome architecture in cerebellar granule cells.

Longzhi Tan, Jenny Shi, Siavash Moghadami, Bibudha Parasar, Cydney P Wright, Yunji Seo, Kristen Vallejo, Inma Cobos, Laramie Duncan, Ritchie Chen and 1 more

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
10.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  8. Reversing aging-like 3D genome disorganization in abioRxiv : the preprint server for biology · 2026
    Article
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  17. Review
  18. Life-long behavioral screen reveals an architecture of vertebrate aging.bioRxiv : the preprint server for biology · 2025
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Longzhi Tan *Department of Neurobiology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-5618-1299
Jenny Shi *Department of Neurobiology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-1643-4789
Siavash MoghadamiDepartment of Neurobiology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-1251-7384
Bibudha ParasarDepartment of Neurobiology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0001-9042-543X
Cydney P WrightDepartment of Neurobiology, Stanford University, Stanford, CA 94305, USA.ORCID 0009-0007-4849-0503
Yunji SeoDepartment of Neurobiology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-0314-1805
Kristen VallejoDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0009-0005-1418-7931
Inma CobosDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-2043-1890
Laramie DuncanDepartment of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305, USA.
Ritchie ChenDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Karl DeisserothDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0001-9440-3967
Stanford University · USHoward Hughes Medical Institute · US

Funding

Stanford Alzheimer's Disease Research CenterAdmin Supp: Developing iPSC models for AD and PDP30AG066515 · NIA · STANFORD UNIVERSITY · PI LU TIAN · 2020 to 2026
$29.0M
Sex hormones and post-traumatic stress disorder (PTSD)R01MH123486 · NIMH · STANFORD UNIVERSITY · PI DUNCAN, LARAMIE · 2020 to 2024
$2.1M
Molecular Pharmacology Training ProgramT32GM136631 · NIGMS · STANFORD UNIVERSITY · PI BOGYO, MATTHEW, CHEN, JAMES K · 2021 to 2025
$2.0M
Sex Chromosome GWAS of Post-Traumatic Stress Disorder (PTSD)R21MH125358 · NIMH · STANFORD UNIVERSITY · PI DUNCAN, LARAMIE · 2021 to 2022
$443k
Noninvasive Optogenetic Interventions for EpilepsyK99NS119784 · NINDS · STANFORD UNIVERSITY · PI CHEN, RITCHIE · 2021 to 2022
$245k
Howard Hughes Medical InstituteNIA NIH HHS P30 AG066515NIGMS NIH HHS T32 GM136631NIMH NIH HHS R01 MH123486NIMH NIH HHS R21 MH125358NINDS NIH HHS K99 NS119784
6 · The paper itself

Abstract

The cerebellum contains most of the neurons in the human brain and exhibits distinctive modes of development and aging. In this work, by developing our single-cell three-dimensional (3D) genome assay-diploid chromosome conformation capture, or Dip-C-into population-scale (Pop-C) and virus-enriched (vDip-C) modes, we resolved the first 3D genome structures of single cerebellar cells, created life-spanning 3D genome atlases for both humans and mice, and jointly measured transcriptome and chromatin accessibility during development. We found that although the transcriptome and chromatin accessibility of cerebellar granule neurons mature in early postnatal life, 3D genome architecture gradually remodels throughout life, establishing ultra-long-range intrachromosomal contacts and specific interchromosomal contacts that are rarely seen in neurons. These results reveal unexpected evolutionarily conserved molecular processes that underlie distinctive features of neural development and aging across the mammalian life span.

Indexed as

Cellular SenescenceCerebellumChromatin Assembly and DisassemblyGenomeNeuronsAnimalsAtlases as TopicHumansImaging, Three-DimensionalMiceSingle-Cell Analysis

Identifiers

PMID37676945
PMCPMC11059189
OpenAlexW4386523929

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.