FUNCTION OF GLI GENES IN SHH SIGNALING

GLI 基因在 SHH 信号传导中的功能

基本信息

项目摘要

The hedgehog (hh) signaling pathway is implicated in patterning both invertebrate and vertebrate embryos. Genetic analysis in Drosophila established that the cubitus interruptus (ci) is the most downstream component of the signaling pathway. There are three ci homologs in vertebrate, Gli1, Gli2 and Gli3. The overall goal of the proposal is to determine the distinct and yet overlapping function of these three Gli genes in hh signaling pathway by using the knock-in approach. Specifically, the endogenous coding sequence of Gli2 will be replaced by that of Gli1 and Gli3. This project will be done in three steps. First, the 5' region of Gli2 genomic region will be analyzed to select a knock-in site. In the meantime, Gli1 and Gli3 knock-in construct will be made and tested in Sonic hedgehog responsive cell line MNS70. In the second step, knock-in constructs will be introduced into embryonic stem cells. Chimeric embryos and germline mutant mice will be generated. Finally, the phenotypes associated with heterozygous and homozygous mutant mice will be analyzed by using various marker genes in the spinal cord, lung and skeleton. Studies on the function of Gli genes have direct relevance to human development and disease since homolog of these three genes exist in humans and mutations in these genes have been implicated in cancers and developmental defects.
hedgehog (hh)信号通路涉及无脊椎动物和脊椎动物胚胎的模式。果蝇的遗传分析表明,cubitus interruptus (ci)是信号通路中最下游的部分。在脊椎动物中有Gli1、Gli2和Gli3三个同源蛋白。该建议的总体目标是通过敲入方法确定这三个Gli基因在hh信号通路中的不同而又重叠的功能。具体来说,Gli2的内源性编码序列将被Gli1和Gli3的编码序列所取代。这个项目将分三步完成。首先,分析Gli2基因组区域的5′区,选择敲入位点。同时,Gli1和Gli3的敲入构建将在Sonic hedgehog反应细胞系MNS70中进行测试。第二步,敲入结构将被引入胚胎干细胞。将产生嵌合胚胎和种系突变小鼠。最后,利用脊髓、肺和骨骼中的各种标记基因分析杂合子和纯合子突变小鼠的相关表型。Gli基因的功能研究与人类发育和疾病有直接关系,因为这三个基因在人类中存在同源性,并且这些基因的突变与癌症和发育缺陷有关。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Chunyang Brian Bai其他文献

Chunyang Brian Bai的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Chunyang Brian Bai', 18)}}的其他基金

High content screening to identify therapeutics for multiple sclerosis
高内涵筛查以确定多发性硬化症的治疗方法
  • 批准号:
    8543776
  • 财政年份:
    2012
  • 资助金额:
    $ 4.02万
  • 项目类别:
High content screening to identify therapeutics for multiple sclerosis
高内涵筛查以确定多发性硬化症的治疗方法
  • 批准号:
    8312253
  • 财政年份:
    2012
  • 资助金额:
    $ 4.02万
  • 项目类别:
FUNCTION OF GLI GENES IN SHH SIGNALING
GLI 基因在 SHH 信号传导中的功能
  • 批准号:
    6476677
  • 财政年份:
    2001
  • 资助金额:
    $ 4.02万
  • 项目类别:
FUNCTION OF GLI GENES IN SHH SIGNALING
GLI 基因在 SHH 信号传导中的功能
  • 批准号:
    6013262
  • 财政年份:
    2000
  • 资助金额:
    $ 4.02万
  • 项目类别:

相似海外基金

CAREER: Elucidating spatial and epigenetic regulation of gene expression during human development using photopatterning and single-cell multiomics
职业:利用光模式和单细胞多组学阐明人类发育过程中基因表达的空间和表观遗传调控
  • 批准号:
    2339849
  • 财政年份:
    2024
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Continuing Grant
CAREER: Scalable algorithms for regularized and non-linear genetic models of gene expression
职业:基因表达的正则化和非线性遗传模型的可扩展算法
  • 批准号:
    2336469
  • 财政年份:
    2024
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Continuing Grant
CAREER: Epigenetic Regulation of Gene Expression in Engineered Prokaryotes
职业:工程原核生物基因表达的表观遗传调控
  • 批准号:
    2338573
  • 财政年份:
    2024
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Continuing Grant
MFB: RNA modifications of frameshifting stimulators: cellular platforms to engineer gene expression by computational mutation predictions and functional experiments
MFB:移码刺激器的RNA修饰:通过计算突变预测和功能实验来设计基因表达的细胞平台
  • 批准号:
    2330628
  • 财政年份:
    2024
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Standard Grant
22-BBSRC/NSF-BIO Building synthetic regulatory units to understand the complexity of mammalian gene expression
22-BBSRC/NSF-BIO 构建合成调控单元以了解哺乳动物基因表达的复杂性
  • 批准号:
    BB/Y008898/1
  • 财政年份:
    2024
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Research Grant
How does the chromatin remodeller CHD4 regulate gene expression?
染色质重塑因子 CHD4 如何调节基因表达?
  • 批准号:
    DP240102119
  • 财政年份:
    2024
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Discovery Projects
Application for 2024 CIHR NIF (ECR): Investigating the role of SARS-CoV-2 and MERS-CoV transcription regulatory sequence (TRS) in viral gene expression and virulence
2024 CIHR NIF (ECR) 申请:研究 SARS-CoV-2 和 MERS-CoV 转录调控序列 (TRS) 在病毒基因表达和毒力中的作用
  • 批准号:
    491942
  • 财政年份:
    2023
  • 资助金额:
    $ 4.02万
  • 项目类别:
Regulation of gene expression by the La and La-related proteins
La 和 La 相关蛋白对基因表达的调节
  • 批准号:
    489704
  • 财政年份:
    2023
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Operating Grants
Investigating the role of SARS-CoV-2 and MERS-CoV transcription regulatory sequence (TRS) in viral gene expression and virulence
研究 SARS-CoV-2 和 MERS-CoV 转录调控序列 (TRS) 在病毒基因表达和毒力中的作用
  • 批准号:
    494272
  • 财政年份:
    2023
  • 资助金额:
    $ 4.02万
  • 项目类别:
    Operating Grants
Data-driven model links BMIz to gene expression in pediatric asthma
数据驱动模型将 BMIz 与小儿哮喘基因表达联系起来
  • 批准号:
    493135
  • 财政年份:
    2023
  • 资助金额:
    $ 4.02万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了