课题基金 / 基金详情

Transcriptional regulation of Sox9 in chondrogenesis

Transcriptional regulation of Sox9 in chondrogenesis
Sox9 在软骨形成中的转录调控
批准号:
8396774
负责人:
Timothy Joseph Mead
金额:
$4.92万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-02-01 至 2016-01-31

项目摘要

项目成果

Timothy Joseph Mead的其他基金

相似基金

相关文献

中文摘要
翻译
描述(申请人提供):在软骨形成或成人维持过程中的遗传性和获得性缺陷会导致多种类型的骨骼发育不良和关节退行性疾病,即骨关节炎。SOX9编码一种软骨形成所必需的转录因子。然而,软骨细胞中Sox9转录的潜在机制在很大程度上仍不清楚。SOX9增强剂已被确定用于发育性腺、神经脊和脊髓,但尚未发现用于软骨细胞的增强剂。该研究项目的首要目标是确定Sox9在软骨细胞中表达的机制。我们已经确定了位于Sox9启动子上游的一个高度保守的增强子。转基因小鼠的初步结果表明,该增强剂对软骨原基和生长板中的增殖软骨细胞具有活性。我认为这种增强子结合的蛋白质对确保Sox9在这些细胞中的表达具有关键作用,因此需要维持软骨细胞的分化,确保骨骼生长和及时成骨。这个项目的主要目的是通过追求以下三个具体目标来验证这一假说:(1)确定体内增强子的活性区域,(2)测试体内表达Sox9是否需要该增强子,以及(3)确定与Sox9增强子结合并激活Sox9增强子的转录因子,并确定它们在软骨形成中的重要性。了解Sox9在软骨形成中表达的分子基础将确定潜在的药物治疗靶点,这可能对骨骼发育不良和退行性软骨疾病(如骨关节炎)的治疗具有临床意义。 公共卫生相关性:软骨成分和调节因素的缺陷会导致许多类型的骨骼畸形疾病(骨骼发育不良)和普遍存在的关节退行性疾病,如骨关节炎。这项新颖的研究旨在确定Sox9表达所需的机制,Sox9是软骨发育所需的基因。从这项研究中获得的知识将使在为治疗策略生成功能软骨方面取得重大进展。
英文摘要
DESCRIPTION (provided by applicant): Inherited and acquired defects in the formation or adult maintenance of cartilage cause many types of skeletal dysplasias and joint degeneration diseases, namely osteoarthritis. Sox9 encodes a transcription factor that is absolutely required for cartilage formation. The mechanisms underlying Sox9 transcription in chondrocytes, however, remain largely unknown. Sox9 enhancers have been identified for developing gonad, neural crest, and spinal cord, but none have been discovered for chondrocytes. The overarching goal of the research project is to identify the mechanisms underlying Sox9 expression in chondrocytes. We have identified a highly conserved enhancer located far upstream of the Sox9 promoter. Preliminary results in transgenic mice indicate that this enhancer is active in proliferative chondrocytes in cartilage primordia and growth plates. I propose that this enhancer binds proteins that have a key role in ensuring Sox9 expression in these cells and are thereby required to maintain chondrocyte differentiation and ensure skeletal growth and timely ossification. The main goal of this project is to test this hypothesis by pursuing the following three specific aims: (1) define the domain of activity of the enhancer in vivo, (2) test whether th enhancer is required for Sox9 expression in vivo, and (3) identify the transcription factors that bind to and activate the Sox9 enhancer, and to determine their importance in chondrogenesis. Understanding the molecular basis of Sox9 expression in chondrogenesis will identify potential pharmacological therapeutic targets, which may have clinical implications for the treatment of skeletal dysplasias and degenerative cartilage diseases such as osteoarthritis. PUBLIC HEALTH RELEVANCE: Defects in cartilage components and regulatory factors cause many types of skeletal malformation diseases (skeletal dysplasias) and prevalent joint degeneration diseases, such as osteoarthritis. This novel study aims to identify the mechanisms that are required for Sox9 expression, a gene that is required for cartilage development. Knowledge obtained from this study will allow major progress to be made to generate functional cartilage for therapeutic strategies.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Impact of microfibril turnover on vascular development and disease
  • 批准号:
    10362098
  • 项目类别:
  • 资助金额:
    $40.25万
  • 财政年份:
    2021
  • 负责人:
    Timothy Joseph Mead
  • 依托单位:
Impact of microfibril turnover on vascular development and disease
  • 批准号:
    10741427
  • 项目类别:
  • 资助金额:
    $40.25万
  • 财政年份:
    2021
  • 负责人:
    Timothy Joseph Mead
  • 依托单位:
Transcriptional regulation of Sox9 in chondrogenesis
  • 批准号:
    8546681
  • 项目类别:
  • 资助金额:
    $5.33万
  • 财政年份:
    2013
  • 负责人:
    Timothy Joseph Mead
  • 依托单位:
海外基金