Evidence map›Paper›PMID 37986891›Full record

ArticlebioRxiv : the preprint server for biology2023

Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.

Sonia Nan Kim, Vinayak V Viswanadham, Ryan N Doan, Yanmei Dou, Sara Bizzotto, Sattar Khoshkhoo, August Yue Huang, Rebecca Yeh, Brian Chhouk, Alex Truong and 13 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 29 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 3 institutions in 2 countries.

Sonia Nan KimDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0002-2998-2621
Vinayak V ViswanadhamDepartment of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.ORCID 0000-0002-0236-6490
Ryan N DoanDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0003-1992-5698
Yanmei DouDepartment of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.ORCID 0000-0002-9328-1731
Sara BizzottoDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0001-6644-0306
Sattar KhoshkhooDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0003-3348-557X
August Yue HuangDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0002-0416-2854
Rebecca YehDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Brian ChhoukDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Alex TruongResearch Computing, Harvard Medical School, Boston, 02115, MA, USA.
Kathleen M ChappellResearch Computing, Harvard Medical School, Boston, 02115, MA, USA.
Marc BeaudinDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Alison BartonDepartment of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.ORCID 0000-0003-0882-0196
Shyam K AkulaDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0003-2334-591X
Lariza RentoDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Michael LodatoDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0003-4175-1073
Javier GanzDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0002-2370-9819
Ryan A SzetoProgram in Biological and Biomedical Sciences, Harvard Medical School, Boston, 02115, MA, USA.
Pengpeng LiDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Jessica W TsaiDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Robert Sean HillDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
Peter J ParkDepartment of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.ORCID 0000-0001-9378-960X
Christopher A WalshDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.ORCID 0000-0002-0156-2238
Broad Institute · USHarvard University · USHoward Hughes Medical Institute · US

Funding

RESEARCH TRAINING-MEDICAL INFORMATICS 90T15LM007092 · NLM · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI Nils Gehlenborg · 1992 to 2026
$32.8M
Cell Identity Determination In Human Brain: Somatic Mutation and Cell LineageR01NS032457 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Alice Eunjung Lee, Christopher A. Walsh · 1995 to 2026
$12.7M
1/2-Somatic mosaicism and autism spectrum disorderU01MH106883 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI PARK, PETER J, WALSH, CHRISTOPHER A. · 2015 to 2019
$9.2M
Genetic and Cellular Mechanisms of Temporal Lobe EpilepsyK08NS128272 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI Sattar Khoshkhoo · 2022 to 2026
$1.2M
Characterizing mechanisms and consequences of intergenic transcription in human cancersF31CA264958 · NCI · HARVARD MEDICAL SCHOOL · PI VISWANADHAM, VINAYAK VENKATASESHA · 2021 to 2022
$60k
NCI NIH HHS F31 CA264958NIMH NIH HHS U01 MH106883NINDS NIH HHS K08 NS128272NINDS NIH HHS L30 NS118655NINDS NIH HHS R01 NS032457NLM NIH HHS T15 LM007092
6 · The paper itself

Abstract

The mammalian cerebral cortex shows functional specialization into regions with distinct neuronal compositions, most strikingly in the human brain, but little is known in about how cellular lineages shape cortical regional variation and neuronal cell types during development. Here, we use somatic single nucleotide variants (sSNVs) to map lineages of neuronal sub-types and cortical regions. Early-occurring sSNVs rarely respect Brodmann area (BA) borders, while late-occurring sSNVs mark neuron-generating clones with modest regional restriction, though descendants often dispersed into neighboring BAs. Nevertheless, in visual cortex, BA17 contains 30-70% more sSNVs compared to the neighboring BA18, with clones across the BA17/18 border distributed asymmetrically and thus displaying different cortex-wide dispersion patterns. Moreover, we find that excitatory neuron-generating clones with modest regional restriction consistently share low-mosaic sSNVs with some inhibitory neurons, suggesting significant co-generation of excitatory and some inhibitory neurons in the dorsal cortex. Our analysis reveals human-specific cortical cell lineage patterns, with both regional inhomogeneities in progenitor proliferation and late divergence of excitatory/inhibitory lineages.

Indexed as

cortical developmentexcitatory neuronsinhibitory neuronsinterneuronslineage tracingsingle-cell transcriptomicsSomatic mutationsspatial genomicsvisual cortex

Identifiers

PMID37986891
PMCPMC10659282
OpenAlexW4388457623

What OpenQuestion holds

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LicenceCC BY-ND
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.