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ABSTRACT The goal of the work outline in this proposal is to understand the fundamental signaling that controls cell fate to maintain tissue homeostasis. Epithelial tissues demonstrate an intrinsic ability for their constituent cells to organize and maintain a steady-state of form and function. Many disease states lack these intrinsic controls. Epithelial tissues of the human body are in a constant state of renewal. Our understanding of the signaling systems that control how these complex epithelial tissues maintain robust organization is incomplete. Essential for progress, we need a quantitative understanding of signaling at the single-cell level in the context of physiological conditions to reveal systems-level behaviors that can be targeted therapeutically. We focus on protein kinases as critical mediators of signaling in the cell, which are well known to play prominent roles in tissue function and drivers of disease. Our kinome-wide studies have identified GSK3 and CLK3 as major tissue homeostasis regulators that govern the balance between proliferation and differentiation. In Project 1, we hypothesize GSK3 requires multiple suppressive inputs that uniquely produce different fate outcomes ranging from stem cells, transit-amplifying, and differentiated. We will provide the first systems-level mapping for multiple inputs onto GSK3 dynamics and how these dynamics are decoded into distinct cellular outcomes of renewing epithelium. In Project 2, we hypothesize CLK3 is a gatekeeper controlling stem cell fate through transcriptome regulation. We will define the activity of CLK3 in the stem cell niche as a regulator of expression and splicing of Wnt-target genes to promote stemness. Our approach uses high-throughput quantitative microscopy to measure single-cell behaviors in physiological organoid homeostatic culture models. Our research will define the regulatory mechanisms for two critical kinases, GSK3 and CLK3, and discover novel signaling circuitry needed for the accurate organization of renewing and regenerative epithelia, uncovering new strategies for treating diseases of regenerative tissues.
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SGRN: A Cas12a-driven Synthetic Gene Regulatory Network System.
SGRN:Cas12a 驱动的合成基因调控网络系统。
DOI: 10.1101/2023.05.08.539911
发表时间: 2023
期刊: bioRxiv : the preprint server for biology
影响因子: --
作者: [Kang,HyunJin, Fitch,JohnC, Varghese,ReebaP, Thorne,CurtisA, Cusanovich,DarrenA]
通讯作者: Cusanovich,DarrenA
Defining signaling networks in epithelial homeostasis
  • 批准号:
    10676190
  • 项目类别:
  • 资助金额:
    $37.68万
  • 财政年份:
    2022
  • 负责人:
    Curtis Andrew Thorne
  • 依托单位:
The role of kinase signaling in intestinal epithelial homeostasis
  • 批准号:
    8768122
  • 项目类别:
  • 资助金额:
    $9.0万
  • 财政年份:
    2014
  • 负责人:
    Curtis Andrew Thorne
  • 依托单位:
The role of kinase signaling in intestinal epithelial homeostasis
  • 批准号:
    8920569
  • 项目类别:
  • 资助金额:
    $8.72万
  • 财政年份:
    2014
  • 负责人:
    Curtis Andrew Thorne
  • 依托单位:
国内基金
海外基金
Journal of Integrative Plant Biology
  • 批准号:
    31024801
  • 项目类别:
    专项基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2010
  • 负责人:
    贺萍
  • 依托单位: