TY - JOUR
T1 - Variation in Activity State, Axonal Projection, and Position Define the Transcriptional Identity of Individual Neocortical Projection Neurons
AU - Chevée, Maxime
AU - Robertson, Johanna De Jong
AU - Cannon, Gabrielle Heather
AU - Brown, Solange Pezon
AU - Goff, Loyal Andrew
N1 - Funding Information:
We thank Hao Zhang and the Johns Hopkins Bloomberg School of Public Health Flow Cytometry and Cell Sorting Core Facility. Sequencing service was provided by the Johns Hopkins Genetic Resources Core Facility. We thank Dr. Joshua R. Sanes, Harvard University, for the anti-LacZ antibody and Dr. Jesse Gray, Harvard Medical School, for the curated list of neuronal activity-induced genes. This work was supported by a Klingenstein-Simons Fellowship (to S.P.B.), a Johns Hopkins Science of Learning grant (to S.P.B. and L.A.G.), a National Science Foundation grant ( IOS-1656592 to S.P.B. and L.A.G.), an NIH training grant ( T32 GM07814 to J.D.R.), a Boerhinger-Ingelheim Fonds Fellowship (to M.C.), and a National Institute of Neurological Disorders and Stroke (NINDS) grant ( NS050274 ).
Funding Information:
We thank Hao Zhang and the Johns Hopkins Bloomberg School of Public Health Flow Cytometry and Cell Sorting Core Facility. Sequencing service was provided by the Johns Hopkins Genetic Resources Core Facility. We thank Dr. Joshua R. Sanes, Harvard University, for the anti-LacZ antibody and Dr. Jesse Gray, Harvard Medical School, for the curated list of neuronal activity-induced genes. This work was supported by a Klingenstein-Simons Fellowship (to S.P.B.), a Johns Hopkins Science of Learning grant (to S.P.B. and L.A.G.), a National Science Foundation grant (IOS-1656592 to S.P.B. and L.A.G.), an NIH training grant (T32 GM07814 to J.D.R.), a Boerhinger-Ingelheim Fonds Fellowship (to M.C.), and a National Institute of Neurological Disorders and Stroke (NINDS) grant (NS050274).
Publisher Copyright:
© 2017 The Author(s)
PY - 2018
Y1 - 2018
N2 - Single-cell RNA sequencing has generated catalogs of transcriptionally defined neuronal subtypes of the brain. However, the cellular processes that contribute to neuronal subtype specification and transcriptional heterogeneity remain unclear. By comparing the gene expression profiles of single layer 6 corticothalamic neurons in somatosensory cortex, we show that transcriptional subtypes primarily reflect axonal projection pattern, laminar position within the cortex, and neuronal activity state. Pseudotemporal ordering of 1,023 cellular responses to sensory manipulation demonstrates that changes in expression of activity-induced genes both reinforced cell-type identity and contributed to increased transcriptional heterogeneity within each cell type. This is due to cell-type biased choices of transcriptional states following manipulation of neuronal activity. These results reveal that axonal projection pattern, laminar position, and activity state define significant axes of variation that contribute both to the transcriptional identity of individual neurons and to the transcriptional heterogeneity within each neuronal subtype. Chevée et al. find that sources of transcriptional heterogeneity defining cortical projection neurons include axonal projection pattern, laminar position, and activity state. Altering activity state through sensory manipulation increased cell-to-cell variation within cell types and enhanced distinctions between cell types.
AB - Single-cell RNA sequencing has generated catalogs of transcriptionally defined neuronal subtypes of the brain. However, the cellular processes that contribute to neuronal subtype specification and transcriptional heterogeneity remain unclear. By comparing the gene expression profiles of single layer 6 corticothalamic neurons in somatosensory cortex, we show that transcriptional subtypes primarily reflect axonal projection pattern, laminar position within the cortex, and neuronal activity state. Pseudotemporal ordering of 1,023 cellular responses to sensory manipulation demonstrates that changes in expression of activity-induced genes both reinforced cell-type identity and contributed to increased transcriptional heterogeneity within each cell type. This is due to cell-type biased choices of transcriptional states following manipulation of neuronal activity. These results reveal that axonal projection pattern, laminar position, and activity state define significant axes of variation that contribute both to the transcriptional identity of individual neurons and to the transcriptional heterogeneity within each neuronal subtype. Chevée et al. find that sources of transcriptional heterogeneity defining cortical projection neurons include axonal projection pattern, laminar position, and activity state. Altering activity state through sensory manipulation increased cell-to-cell variation within cell types and enhanced distinctions between cell types.
KW - activity-dependent plasticity
KW - barrel cortex
KW - corticothalamic neurons
KW - neocortex
KW - neuronal identity
KW - single-cell RNA sequencing
KW - somatosensory cortex
KW - transcriptional variation
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U2 - 10.1016/j.celrep.2017.12.046
DO - 10.1016/j.celrep.2017.12.046
M3 - Article
C2 - 29320739
AN - SCOPUS:85041194061
SN - 2211-1247
VL - 22
SP - 441
EP - 455
JO - Cell Reports
JF - Cell Reports
IS - 2
ER -