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DESCRIPTION (provided by applicant): Abnormal proliferation and differentiation of neural progenitors in the developing cerebral cortex can cause brain malformation and result in dysregulation of brain function such as epilepsy and mental retardation. Emerging evidence has shown that similar to protein coding genes, noncoding microRNAs (miRNAs) play critical roles in cortical development and are associated with the etiology of human neurological disorders. Our previous studies have demonstrated miRNA functions in cortical development by generating Dicer conditional knockout mice, in which miRNA biogenesis is specifically blocked in the embryonic cortex. We have identified potential miRNA target genes using proteomic approaches and RNA sequencing technique. We have also examined the role of specific miRNAs in cortical development. miRNAs are often located in the intronic regions of coding genes and transcribed together with host genes. However, the knowledge gap is how intronic miRNAs interact with target genes and host genes, and how expressions of miRNAs, target genes and host genes are precisely and properly regulated during cortical development. In this project, we will test a hypothesis that a regulatory loop of miRNAs, their target genes and host genes works cohesively to ensure proper development of neural progenitors in the developing cortex. Our preliminary study has identified a family of intronic miRNAs that is expressed in the developing mouse cortex. We have developed new tools to alter miRNA expression levels and to examine the specificity of miRNA silencing effects on target genes in vitro and in vivo during cortical development. Based on these findings, our proposed research focuses on three specific aims: Aim 1 is to determine the role of this miRNA family in controlling neural progenitor proliferation and differentiation in vivo and in a culture system. Aim 2 is to elucidate molecular mechanisms of the miRNA regulation by identifying specific target genes. Aim 3 is to reveal the feedback regulation of the miRNA target gene on expression of this miRNA and its host gene in the process of controlling accurate numbers of cortical neural progenitors and proper neurogenesis. Our proposal will address a fundamental question of how a regulatory loop of miRNAs, their target genes and host genes controls proper cortical development. The success of our project should allow us to generate new tools to manipulate expressions of miRNAs and their target genes in vitro and in vivo. Because proper development of cortical neural progenitors is essential for normal brain function, our proposal should provide significant insights into developing a new diagnostic and therapeutic means using miRNAs for human brain malformations and neurological disorders.
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A Circuit Mechanism for the Development of Cortico-cortical Connectivity
  • 批准号:
    10469418
  • 项目类别:
  • 资助金额:
    $50.68万
  • 财政年份:
    2020
  • 负责人:
    Natalia Vanesa De Marco Garcia
  • 依托单位:
A Circuit Mechanism for the Development of Cortico-cortical Connectivity
  • 批准号:
    10680437
  • 项目类别:
  • 资助金额:
    $51.09万
  • 财政年份:
    2020
  • 负责人:
    Natalia Vanesa De Marco Garcia
  • 依托单位:
GABAergic Interneuron Dysfunction in Developing Cortical Circuits Underlying Autism Spectrum Disorders
  • 批准号:
    10306380
  • 项目类别:
  • 资助金额:
    $42.18万
  • 财政年份:
    2020
  • 负责人:
    Natalia Vanesa De Marco Garcia
  • 依托单位:
A Circuit Mechanism for the Development of Cortico-cortical Connectivity
  • 批准号:
    10267037
  • 项目类别:
  • 资助金额:
    $51.1万
  • 财政年份:
    2020
  • 负责人:
    Natalia Vanesa De Marco Garcia
  • 依托单位:
海外基金