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PLoS Genet ; 17(3): e1009355, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33760820

RESUMO

Neurogenesis in the developing neocortex begins with the generation of the preplate, which consists of early-born neurons including Cajal-Retzius (CR) cells and subplate neurons. Here, utilizing the Ebf2-EGFP transgenic mouse in which EGFP initially labels the preplate neurons then persists in CR cells, we reveal the dynamic transcriptome profiles of early neurogenesis and CR cell differentiation. Genome-wide RNA-seq and ChIP-seq analyses at multiple early neurogenic stages have revealed the temporal gene expression dynamics of early neurogenesis and distinct histone modification patterns in early differentiating neurons. We have identified a new set of coding genes and lncRNAs involved in early neuronal differentiation and validated with functional assays in vitro and in vivo. In addition, at E15.5 when Ebf2-EGFP+ cells are mostly CR neurons, single-cell sequencing analysis of purified Ebf2-EGFP+ cells uncovers molecular heterogeneities in CR neurons, but without apparent clustering of cells with distinct regional origins. Along a pseudotemporal trajectory these cells are classified into three different developing states, revealing genetic cascades from early generic neuronal differentiation to late fate specification during the establishment of CR neuron identity and function. Our findings shed light on the molecular mechanisms governing the early differentiation steps during cortical development, especially CR neuron differentiation.


Assuntos
Diferenciação Celular , Genômica , Neurogênese/genética , Neurônios/metabolismo , Lobo Temporal/metabolismo , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Biomarcadores , Diferenciação Celular/genética , Células Cultivadas , Córtex Cerebral/metabolismo , Expressão Gênica , Regulação da Expressão Gênica , Genes Reporter , Heterogeneidade Genética , Genômica/métodos , Histonas , Imuno-Histoquímica , Camundongos , Camundongos Transgênicos , Neurônios/citologia , RNA Longo não Codificante/genética , Análise de Célula Única , Fatores de Transcrição , Sítio de Iniciação de Transcrição
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