SINGLE SUTURE CRANIOSYNOSTOSIS: CANDIDATE GENE AND PATHWAY DISCOVERY

单缝颅缝早闭：候选基因和通路的发现

• 批准号: 8044794
• 负责人: MICHAEL L CUNNINGHAM
• 金额: $ 16.69万
• 依托单位: SEATTLE CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-03-25 至 2013-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8044794
• 关键词: Address; Affect; Calvaria; Candidate Disease Gene; Code; Complex; Congenital abnormal Synostosis; Counseling; Craniosynostosis; DNA Resequencing; Data; Development; Developmental Gene; Diagnosis; FGFR1 gene; FGFR2 gene; FGFR3 gene; Face; Family; Fibroblast Growth Factor Receptors; Frequencies; Functional RNA; Future; Gene Expression; Genes; Genetic; Genomics; Growth; Human; International; Intracranial Hypertension; Investigation; Joint structure of suture of skull; Knowledge; Laboratories; Large-Scale Sequencing; Live Birth; Measures; Microarray Analysis; Modeling; Molecular; Morbidity - disease rate; Mus; Mutate; Mutation; Neurocognitive; Osteoblasts; Pathogenesis; Pathologic; Pathway interactions; Patients; Pattern; Play; Positioning Attribute; Promoter Regions; Reconstructive Surgical Procedures; Regulation; Research; Role; Series; Shapes; Surgical Management; Surgical sutures; Syndrome; TWIST1 gene; Variant; base; case control; cranium; design; developmental genetics; fetal; gene discovery; genetic variant; genome wide association study; interdisciplinary approach; malformation; mortality; novel; rapid growth; research study; success; text searching

DESCRIPTION (provided by applicant): Craniosynostosis is the pathologic fusion of the calvaria. Over the past ten years significant advances have been made in our understanding of multiple malformation syndromes that involve craniosynostosis. It has been shown that mutations in the fibroblast growth factor receptors (FGFR1-3), TWIST1, MSX2, and the EFNB1 each cause craniosynostosis syndrome in humans. This extensive body of work, carried out in several international laboratories, has significantly impacted how we diagnose and counsel families with syndromic craniosynostosis. Despite the rapid growth of knowledge regarding syndromic forms, the causes of isolated synostosis remain elusive. Though vastly more common than syndromic forms, relatively little research has focused on the molecular pathogenesis of isolated craniosynostosis. The frequency of this group of calvarial malformations, the need for complex surgical management and its associated morbidity make isolated craniosynostosis a candidate for intense scientific investigation. We propose the use of three approaches to identify and characterize candidate genetic causes of isolated craniosynostosis: high throughput genomic sequencing, large-scale microarray expression analysis, and developmental gene expression. We have used knowledge gained from the investigation of normal calvarial development and syndromic forms of craniosynostosis to develop two interrelated hypotheses: (A) Rare sequence variants in two classes of genes result in isolated craniosynostosis: those that regulate suture development and those that, when mutated, cause syndromic craniosynostosis; and (B) Genetic pathways involved in cranial suture development and those impacted in the syndromic craniosynostoses are similarly affected in isolated, non-syndromic craniosynostosis. In this proposal, we describe a series of experiments designed to discover potential molecular causes of isolated craniosynostosis through the identification of rare genetic variants, altered calvarial osteoblast gene expression, and the temporal and spatial expression of candidate genes. The expertise of our research team and the availability of complementary high throughput approaches has allowed for the development of a comprehensive investigation of the genetic and developmental pathogenesis of isolated craniosynostosis.

描述(申请人提供)：颅缝融合是颅骨的病理性融合。在过去的十年里，在我们对涉及颅缝融合的多发性畸形综合征的理解方面取得了重大进展。已有研究表明，成纤维细胞生长因子受体(FGFR1-3)、Twist1、MSX2和EFNB1的突变都会导致人类的颅突融合综合征。这项广泛的工作在几个国际实验室进行，显著影响了我们诊断和咨询患有综合征性颅缝早闭的家庭的方式。尽管关于综合征形式的知识迅速增长，但孤立的联会的原因仍然难以捉摸。虽然远比综合征形式常见，但相对较少的研究集中在孤立性颅缝早闭的分子发病机制上。这组颅骨畸形的频率，需要复杂的手术治疗及其相关的发病率使孤立性颅缝融合症成为密集科学研究的候选对象。我们建议使用三种方法来识别和表征孤立性颅缝早闭的候选遗传原因：高通量基因组测序、大规模微阵列表达分析和发育基因表达。我们利用从颅骨正常发育和颅缝融合综合征的研究中获得的知识，提出了两个相互关联的假说：(A)两类基因中的罕见序列变异导致孤立的颅缝融合：那些调节缝合发育的基因和那些突变时，导致综合征的颅缝融合；以及(B)参与颅缝发育的遗传途径和那些受到综合征颅缝融合影响的基因在孤立的非综合征颅缝融合中也受到类似的影响。在这项建议中，我们描述了一系列实验，旨在通过鉴定罕见的遗传变异、颅骨成骨细胞基因表达的改变以及候选基因的时间和空间表达来发现孤立性颅缝融合症的潜在分子原因。我们研究团队的专业知识和补充的高通量方法的可用性使我们能够对孤立性颅缝融合的遗传和发育发病机制进行全面的调查。