NSF PRFB FY 2023: Development across evolutionary time at a single-cell resolution
NSF PRFB 2023 财年:以单细胞分辨率跨进化时间进行开发
基本信息
- 批准号:2305513
- 负责人:
- 金额:$ 24万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Fellowship Award
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-06-01 至 2026-05-31
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
This action funds an NSF Postdoctoral Research Fellowship in Biology for FY 2023, Integrative Research Investigating the Rules of Life Governing Interactions Between Genomes, Environment, and Phenotypes. The fellowship supports research and training of the fellow that will contribute to the area of Rules of Life in innovative ways. Development from a single-celled egg to an adult animal relies on the coordination and control of thousands of genes that allows them to be turned on and off in the right cell at the right time. How the regulation of these genes changes between organisms through evolution, and results in Earth’s diversity of life remains a fundamental and unanswered question of biology. Comparisons of the gene regulation that controls development between closely related animals reveals that despite superficial similarity, how development is controlled can vary significantly. This project aims to provide insight into the extent by which gene regulation differs across 13 species of closely related and similar roundworms in order to reveal what allows some genes to change and others to stay the same. Overall, the project will use these roundworms as a model system to expand our knowledge of how development evolves across animals more broadly.The fellow will use single-cell sequencing to measure the spatiotemporal divergence of gene expression across evolutionary time within the Caenorhabditis nematodes by comparing the transcriptomes of homologous cells and tissues between species across embryonic development. Taking a systems approach, the fellow will help elucidate the constraints on gene regulatory network evolution by building and comparing molecular atlases of development for 13 Caenorhabditis species. The multispecies single-cell atlases will allow for the determination of the rate of divergence of cell and gene expression patterns across the Caenorhabditis genus to test fundamental models in evolution and development. Additionally, using the data and knowledge gained through this project, the fellow will help train the next generation of scientists through a series of computational biology training workshops for summer undergraduate researchers from underrepresented backgrounds. The fellow will also directly train a diverse group of summer undergraduate researchers in the laboratory.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
这项行动资助了2023财年的NSF生物学博士后研究奖学金,综合研究调查了基因组,环境和表型之间的生命管理相互作用的规则。该研究金支持研究员的研究和培训,以创新的方式为生活规则领域做出贡献。从单细胞卵到成年动物的发育依赖于数千个基因的协调和控制,使它们能够在正确的时间在正确的细胞中打开和关闭。这些基因的调节如何通过进化在生物体之间发生变化,并导致地球上生命的多样性仍然是生物学的一个基本和未回答的问题。对控制密切相关动物之间发育的基因调控进行比较表明,尽管表面上相似,但发育的控制方式可能存在显着差异。该项目旨在深入了解13种密切相关和相似的蛔虫的基因调控差异程度,以揭示是什么允许一些基因发生变化,而另一些基因保持不变。总的来说,该项目将使用这些蛔虫作为模型系统,以扩大我们的知识,如何在动物之间的发展演变更广泛。该研究员将使用单细胞测序,以衡量基因表达的时空差异在进化时间内的小杆线虫通过比较转录组的同源细胞和组织物种之间的胚胎发育。以系统的方法,该研究员将有助于阐明基因调控网络进化的限制,通过建立和比较13个小杆线虫物种的发展的分子图谱。多物种的单细胞图谱将允许跨小杆线虫属的细胞和基因表达模式的分歧率的确定,以测试进化和发展的基本模型。此外,利用通过该项目获得的数据和知识,该研究员将通过为来自代表性不足背景的夏季本科研究人员举办一系列计算生物学培训讲习班,帮助培训下一代科学家。该奖项反映了NSF的法定使命,并通过使用基金会的智力价值和更广泛的影响审查标准进行评估,被认为值得支持。
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)
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Christopher Large其他文献
Functional analysis of branched-chain amino acids (BCAAs) biosynthesis in the yeast Saccharomyces cerevisiae
酿酒酵母支链氨基酸 (BCAA) 生物合成的功能分析
- DOI:
- 发表时间:
2019 - 期刊:
- 影响因子:0
- 作者:
Koonthongkaew Jirasin;Yoichi Toyokawa;Christopher Large;Maitreya Dunham;Hiroshi Takagi - 通讯作者:
Hiroshi Takagi
Christopher Large的其他文献
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