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      Caveolin1 Identifies a Specific Subpopulation of Cerebral Cortex Callosal Projection Neurons (CPN) Including Dual Projecting Cortical Callosal/Frontal Projection Neurons (CPN/FPN)

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          Abstract

          The neocortex is composed of many distinct subtypes of neurons that must form precise subtype-specific connections to enable the cortex to perform complex functions. Callosal projection neurons (CPN) are the broad population of commissural neurons that connect the cerebral hemispheres via the corpus callosum (CC). Currently, how the remarkable diversity of CPN subtypes and connectivity is specified, and how they differentiate to form highly precise and specific circuits, are largely unknown. We identify in mouse that the lipid-bound scaffolding domain protein Caveolin 1 (CAV1) is specifically expressed by a unique subpopulation of Layer V CPN that maintain dual ipsilateral frontal projections to premotor cortex. CAV1 is expressed by over 80% of these dual projecting callosal/frontal projection neurons (CPN/FPN), with expression peaking early postnatally as axonal and dendritic targets are being reached and refined. CAV1 is localized to the soma and dendrites of CPN/FPN, a unique population of neurons that shares information both between hemispheres and with premotor cortex, suggesting function during postmitotic development and refinement of these neurons, rather than in their specification. Consistent with this, we find that Cav1 function is not necessary for the early specification of CPN/FPN, or for projecting to their dual axonal targets. CPN subtype-specific expression of Cav1 identifies and characterizes a first molecular component that distinguishes this functionally unique projection neuron population, a population that expands in primates, and is prototypical of additional dual and higher-order projection neuron subtypes.

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          Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo.

          Within the vertebrate nervous system, the presence of many different lineages of neurons and glia complicates the molecular characterization of single neuronal populations. In order to elucidate molecular mechanisms underlying the specification and development of corticospinal motor neurons (CSMN), we purified CSMN at distinct stages of development in vivo and compared their gene expression to two other pure populations of cortical projection neurons: callosal projection neurons and corticotectal projection neurons. We found genes that are potentially instructive for CSMN development, as well as genes that are excluded from CSMN and are restricted to other populations of neurons, even within the same cortical layer. Loss-of-function experiments in null mutant mice for Ctip2 (also known as Bcl11b), one of the newly characterized genes, demonstrate that it plays a critical role in the development of CSMN axonal projections to the spinal cord in vivo, confirming that we identified central genetic determinants of the CSMN population.
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            Molecular logic of neocortical projection neuron specification, development and diversity.

            The sophisticated circuitry of the neocortex is assembled from a diverse repertoire of neuronal subtypes generated during development under precise molecular regulation. In recent years, several key controls over the specification and differentiation of neocortical projection neurons have been identified. This work provides substantial insight into the 'molecular logic' underlying cortical development and increasingly supports a model in which individual progenitor-stage and postmitotic regulators are embedded within highly interconnected networks that gate sequential developmental decisions. Here, we provide an integrative account of the molecular controls that direct the progressive development and delineation of subtype and area identity of neocortical projection neurons.
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              Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex.

              Pyramidal neurons of the neocortex can be subdivided into two major groups: deep- (DL) and upper-layer (UL) neurons. Here we report that the expression of the AT-rich DNA-binding protein Satb2 defines two subclasses of UL neurons: UL1 (Satb2 positive) and UL2 (Satb2 negative). In the absence of Satb2, UL1 neurons lose their identity and activate DL- and UL2-specific genetic programs. UL1 neurons in Satb2 mutants fail to migrate to superficial layers and do not contribute to the corpus callosum but to the corticospinal tract, which is normally populated by DL axons. Ctip2, a gene required for the formation of the corticospinal tract, is ectopically expressed in all UL1 neurons in the absence of Satb2. Satb2 protein interacts with the Ctip2 genomic region and controls chromatin remodeling at this locus. Satb2 therefore is required for the initiation of the UL1-specific genetic program and for the inactivation of DL- and UL2-specific genes.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                8 January 2018
                18 January 2018
                Jan-Feb 2018
                : 5
                : 1
                : ENEURO.0234-17.2017
                Affiliations
                [1 ]Department of Stem Cell and Regenerative Biology, Center for Brain Science, and Harvard Stem Cell Institute, Harvard University , Cambridge, MA 02138
                [2 ]Department of Biology, Syracuse University, Syracuse, NY 13244
                Author notes

                The authors declare no competing financial interests.

                Author contributions: J.L.M., R.M.F., and J.D.M. designed research; J.L.M., R.M.F., and E.M.G.-B. performed research; J.L.M. and R.M.F. analyzed data; J.L.M., R.M.F., and J.D.M. wrote the paper.

                This work was supported by grants from the National Institutes of Health (R37 NS41590, with additional infrastructure support by NS45523, NS49553, and NS075672), the Jane and Lee Seidman Fund, the Emily and Robert Pearlstein Fund, and the United Sydney Association (to J.D.M); and by the National Science Foundation Graduate Research Fellowship Program fellowship and the National Institutes of Health Predoctoral NRSA Fellowship F31 NS073163 (to R.M.F).

                [§]

                J.L.M. and R.M.F. contributed equally to this work.

                J. L. MacDonald’s present address: Department of Biology, Syracuse University, Syracuse, NY 13244.

                [* ]Correspondence should be addressed to either of the following: Jessica L. MacDonald at the above address, E-mail: jemacdon@ 123456syr.edu ; Jeffrey D. Macklis at the above address, E-mail: jeffrey_macklis@ 123456harvard.edu .
                Author information
                http://orcid.org/0000-0002-9111-5756
                http://orcid.org/0000-0002-8244-2624
                http://orcid.org/0000-0001-5071-9572
                http://orcid.org/0000-0003-3662-9698
                Article
                eN-NWR-0234-17
                10.1523/ENEURO.0234-17.2017
                5780842
                d47b7e98-d648-47cb-a9bf-96429e617fe8
                Copyright © 2018 MacDonald et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 5 July 2017
                : 11 December 2017
                : 19 December 2017
                Page count
                Figures: 6, Tables: 1, Equations: 0, References: 65, Pages: 17, Words: 10606
                Funding
                Funded by: http://doi.org/10.13039/100000065HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS)
                Award ID: R37 NS41590
                Award ID: NS45523
                Award ID: NS49553
                Award ID: NS075672
                Funded by: Jane and Lee Seidman Fund
                Funded by: Emily and Robert Pearlstein Fund
                Funded by: United Sydney Association
                Funded by: http://doi.org/10.13039/100000002HHS | National Institutes of Health (NIH)
                Award ID: F31 NS073163
                Categories
                2
                2.1
                New Research
                Development
                Custom metadata
                January/February

                axonal projections,connectivity,corpus callosum,neocortex,neuronal subtypes

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