Your browser doesn't support javascript.
loading
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
Kim, Sonia Nan; Viswanadham, Vinayak V; Doan, Ryan N; Dou, Yanmei; Bizzotto, Sara; Khoshkhoo, Sattar; Huang, August Yue; Yeh, Rebecca; Chhouk, Brian; Truong, Alex; Chappell, Kathleen M; Beaudin, Marc; Barton, Alison; Akula, Shyam K; Rento, Lariza; Lodato, Michael; Ganz, Javier; Szeto, Ryan A; Li, Pengpeng; Tsai, Jessica W; Hill, Robert Sean; Park, Peter J; Walsh, Christopher A.
Afiliação
  • Kim SN; Division 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.
  • Viswanadham VV; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
  • Doan RN; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Dou Y; Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, 02115, MA, USA.
  • Bizzotto S; Department of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.
  • Khoshkhoo S; Bioinformatics and Integrative Genomics Program, Harvard Medical School, Boston, 02115, MA, USA.
  • Huang AY; Division 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.
  • Yeh R; Department of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.
  • Chhouk B; Division 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.
  • Truong A; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
  • Chappell KM; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Beaudin M; Division 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.
  • Barton A; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Akula SK; Department of Neurology, Brigham and Women's Hospital, Boston, 02115, MA, USA.
  • Rento L; Division 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.
  • Lodato M; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
  • Ganz J; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Szeto RA; Division 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.
  • Li P; Division 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.
  • Tsai JW; Research Computing, Harvard Medical School, Boston, 02115, MA, USA.
  • Hill RS; Research Computing, Harvard Medical School, Boston, 02115, MA, USA.
  • Park PJ; Division 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.
  • Walsh CA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
bioRxiv ; 2023 Nov 06.
Article em En | MEDLINE | ID: mdl-37986891
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.
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos