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      BMPs direct sensory interneuron identity in the developing spinal cord using signal-specific not morphogenic activities

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          Abstract

          The Bone Morphogenetic Protein (BMP) family reiteratively signals to direct disparate cellular fates throughout embryogenesis. In the developing dorsal spinal cord, multiple BMPs are required to specify sensory interneurons (INs). Previous studies suggested that the BMPs act as concentration-dependent morphogens to direct IN identity, analogous to the manner in which sonic hedgehog patterns the ventral spinal cord. However, it remains unresolved how multiple BMPs would cooperate to establish a unified morphogen gradient. Our studies support an alternative model: BMPs have signal-specific activities directing particular IN fates. Using chicken and mouse models, we show that the identity, not concentration, of the BMP ligand directs distinct dorsal identities. Individual BMPs promote progenitor patterning or neuronal differentiation by their activation of different type I BMP receptors and distinct modulations of the cell cycle. Together, this study shows that a ‘mix and match’ code of BMP signaling results in distinct classes of sensory INs.

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            A series of normal stages in the development of the chick embryo. 1951.

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              Directed differentiation of embryonic stem cells into motor neurons.

              Inductive signals and transcription factors involved in motor neuron generation have been identified, raising the question of whether these developmental insights can be used to direct stem cells to a motor neuron fate. We show that developmentally relevant signaling factors can induce mouse embryonic stem (ES) cells to differentiate into spinal progenitor cells, and subsequently into motor neurons, through a pathway recapitulating that used in vivo. ES cell-derived motor neurons can populate the embryonic spinal cord, extend axons, and form synapses with target muscles. Thus, inductive signals involved in normal pathways of neurogenesis can direct ES cells to form specific classes of CNS neurons.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                19 September 2017
                2017
                : 6
                : e30647
                Affiliations
                [1 ]deptDepartment of Neurobiology University of California Los AngelesUnited States
                [2 ]deptNeuroscience Graduate Program University of California Los AngelesUnited States
                [3 ]deptEli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research University of California Los AngelesUnited States
                [4 ]deptCIRM Bridges to Research Program California State University NorthridgeUnited States
                [5 ]deptDepartment of Dermatology University of Southern California CaliforniaUnited States
                California Institute of Technology United States
                California Institute of Technology United States
                Author information
                http://orcid.org/0000-0002-5154-5081
                http://orcid.org/0000-0002-9491-7551
                Article
                30647
                10.7554/eLife.30647
                5605194
                28925352
                fef3476a-660b-456f-9b04-22df92c822d9
                © 2017, Andrews et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 22 July 2017
                : 24 August 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01: NS085097
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000900, California Institute for Regenerative Medicine;
                Award ID: RB5-07320
                Award Recipient :
                Funded by: UCLA Broad Stem Cell Research Center;
                Award ID: Research Grant
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: T32 training fellowship: HD060549
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000900, California Institute for Regenerative Medicine;
                Award ID: Bridges to Research fellowship: TB1-01183
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Developmental Biology and Stem Cells
                Neuroscience
                Custom metadata
                Members of the BMP family of growth factors act as a reiterative code of distinct activities to direct the identities of different classes of sensory neurons in the spinal cord.

                Life sciences
                bone morphogenetic proteins,spinal cord,patterning,cell fate,neurons,morphogen,chicken,mouse
                Life sciences
                bone morphogenetic proteins, spinal cord, patterning, cell fate, neurons, morphogen, chicken, mouse

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