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DESCRIPTION (provided by applicant): The objective is to create a global gene expression atlas of the developing kidney. The central thesis is that a combination of laser capture microdissection and microarrays can be used to efficiently achieve this goal. Microarrays with essentially complete gene representation can be used to rapidly determine the expression levels of every gene in laser capture microdissected elements of the developing kidney. A single experiment, therefore, provides a comprehensive analysis of the gene expression status of one component, and a limited number of experiments examining each structure and substructure can create an atlas. Specific aim 1 is to use this strategy to produce an atlas of the gene expression profiles of specific domains of the developing mouse kidney. The initial focus will be on the E15.5 kidney, which provides a single time point with multiple stages of nephrogenesis, but earlier time points will also be examined. A combination of structure, lectin staining, immunohistochemistry and transgenic GFP expression will be used to precisely identify specific components and lineages. Specific aim 2 is to make transgenic mouse tools to promote both gene expression profiling and functional studies of kidney development. We propose to make a series of transgenic mice with specific promoters driving restricted expression of a Cre-GFP cassette. These mice will serve a dual purpose, to allow identification of additional discreet kidney components for Specific Aim 1 and to aid future domain specific gene knockout studies in the developing kidney. Specific aim 3 is to perform bioinformatics analysis of the microarray data and to make results readily available to the research community. Microarrays produce large gene lists that need to be sifted. Analysis of the complex orchestrations of gene expression defined in Specific Aim 1 will provide deeper insight into the genetic basis of the development of the distinct parts of the nephron.
期刊论文(9)
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会议论文
Defining the genetic blueprint of kidney development.
定义肾脏发育的遗传蓝图。
DOI: 10.1007/s00467-011-1807-z
发表时间: 2011
期刊: Pediatric nephrology (Berlin, Germany)
影响因子: --
作者: [Potter,SSteven, Brunskill,EricW, Patterson,LarryT]
通讯作者: Patterson,LarryT
DOI: 10.1016/j.ydbio.2017.11.006
发表时间: 2018-02-01
期刊: Developmental biology
影响因子: 2.7
作者: [Magella B, Adam M, Potter AS, Venkatasubramanian M, Chetal K, Hay SB, Salomonis N, Potter SS]
通讯作者: Potter SS
DOI: 10.1371/journal.pone.0012034
发表时间: 2010-08-10
期刊: PloS one
影响因子: 3.7
作者: [Brunskill EW, Potter SS]
通讯作者: Potter SS
DOI: 10.1371/journal.pone.0024640
发表时间: 2011
期刊: PloS one
影响因子: 3.7
作者: [Brunskill EW, Georgas K, Rumballe B, Little MH, Potter SS]
通讯作者: Potter SS
6
    Hox Genes & Lineage Infidelity
    • 批准号:
      10160899
    • 项目类别:
    • 资助金额:
      $50.61万
    • 财政年份:
      2019
    • 负责人:
      S. Steven Potter
    • 依托单位:
    Hox Genes & Lineage Infidelity
    • 批准号:
      10004644
    • 项目类别:
    • 资助金额:
      $50.61万
    • 财政年份:
      2019
    • 负责人:
      S. Steven Potter
    • 依托单位:
    LungMap Phase II - Building a multidimensional map of developing human lung
    • 批准号:
      9815541
    • 项目类别:
    • 资助金额:
      $89.73万
    • 财政年份:
      2019
    • 负责人:
      S. Steven Potter
    • 依托单位:
    Recombineering based analysis of Hox function in kidney development
    • 批准号:
      8701721
    • 项目类别:
    • 资助金额:
      $33.93万
    • 财政年份:
      2014
    • 负责人:
      S. Steven Potter
    • 依托单位:
    海外基金