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Collaborative Research URoL: Epigenetics2: Epigenetic pathways to regulate homeostatic resilience: Model-based discovery of rules across diverse mammals

Collaborative Research URoL: Epigenetics2: Epigenetic pathways to regulate homeostatic resilience: Model-based discovery of rules across diverse mammals
合作研究 URoL:表观遗传学2:调节稳态恢复力的表观遗传途径:基于模型的不同哺乳动物规则发现
批准号:
2022007
负责人:
Elinor Karlsson
金额:
$90.32万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-09-01 至 2025-08-31

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中文摘要
翻译
这个项目将研究控制不同物种如何在细胞水平上对环境变化做出反应的生物学规则,以及为什么有些物种比其他物种更健壮。所有物种都会遇到环境变化,但有些物种能忍受对大多数其他物种来说都是危险的极端环境。果蝠在进食和飞行之间能承受血糖的剧烈变化,骆驼能在炎热的沙漠环境中忍受高体温,深潜哺乳动物能在缺氧的情况下长时间潜水。这个项目的目标是通过测量它们的细胞在实验室中对模拟现实世界变化的不断变化的培养条件的反应来了解不同物种是如何应对极端情况的。这将为开发数学模型提供基础,以理解这种耐受性的遗传成分,以及为什么物种之间的反应不同。该项目将为中学生、本科生和研究生提供积极的学习和研究机会,其中包括许多来自历史上服务不足的人群。它将开发六年级课程丰富生物学和计算机编码,为本科生提供参与实验室研究的机会,并支持研究生和博士后研究人员。通过跨院校合作,在不同层次的学生之间建立师徒关系。该项目还将为公众编写和散发外联材料。大多数哺乳动物处于严格和灵活的体内平衡的极端之间,这意味着它们能在不同程度上容忍细胞生化条件的波动。有些物种能忍受细胞条件的极端变化,通常是由于每种生物特有的环境因素。相反,包括人类在内的许多其他物种对细胞条件的变化难以耐受。这个项目将应用一个共同的花园框架来培养来自不同哺乳动物的细胞,以揭示使不同物种的细胞在内部环境变化中健壮的表观遗传反应。RNA-seq, ATAC-seq和细胞形态学和生理学数据将用于分析不同物种的细胞在暴露于可变氧,葡萄糖和温度条件下的反应。通过使用新的比较计算方法和进化框架分析这些数据集,该项目将确定严格内稳态与灵活细胞表型相关的基因。在基于主体的建模方法中,这些基因将被建模为“代理”,以区分“驱动”假设,其稳健性由几个大影响的表观基因型协调,或另一个“小影响”假设,其稳健性由许多单个小影响的表观基因型产生,以及在少数与许多进化路径之间的可能性之间达到给定的稳健性表型。这种跨学科的合作将开创一种新的策略,发现细胞缓冲能力的本质和极限,这种缓冲能力是极端表型的基础,并揭示哺乳动物细胞应对环境变化的“规则”。该项目由理解生命规则:表观遗传学项目资助,该项目由生物科学理事会新兴前沿部门管理,是NSF十大理念的一部分。该奖项反映了美国国家科学基金会的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
This project will examine biological rules that govern how different species respond, at the cellular level, to changes in their environment, and why some species are more robust than others. All species encounter environmental variation, but some tolerate extremes that would be dangerous to most other species. Fruit bats withstand dramatic changes in blood glucose between feeding and flying, camels tolerate high body temperatures in hot desert environments, and deep-diving mammals survive with little oxygen during long dives. The goal of this project is to understand how diverse species cope with extremes by measuring how their cells respond in the lab to changing culture conditions that mimic real-world variation. This will provide a foundation for developing mathematical models to understand the genetic components of this tolerance, and why the response differs between species. This project will provide active learning and research opportunities for middle school, undergraduate and graduate students, including many from historically underserved populations. It will develop sixth grade curricular enrichment in biology and computer coding, provide opportunities for undergraduate students to participate in laboratory research, and support graduate students and postdoctoral researchers. Through cross-institutional collaborations, it will establish mentoring relationships between students at different levels. This project will also develop and disseminate outreach materials for the general public.Most mammals lie somewhere between the extremes of strict and flexible homeostasis, meaning that they tolerate fluctuations in cellular biochemical conditions to varying degrees. Some species tolerate extreme variation in cellular conditions, often for environmental factors that are specific to each organism. Conversely, variation in cellular conditions is poorly tolerated by many other species, including humans. This project will apply a common-garden framework to cultured cells from diverse mammals to uncover epigenetic responses that render cells of diverse species robust to variation in the internal milieu. RNA-seq, ATAC-seq, and cellular morphology and physiology data will be used to assay the responses of cells from different species when exposed to a panel of variable oxygen, glucose, and temperature conditions. By analyzing these datasets using new comparative computational approaches and an evolutionary framework, the project will identify genes involved in strictly homeostatic versus flexible cellular phenotypes. These genes will be modeled as “agents” in an agent-based modeling approach to distinguish between a "driver" hypothesis, with robustness coordinated by a few epigenotypes of large effect, or an alternate "small-impact" hypothesis, with robustness arising from many epigenotypes of individually small effect, and between the possibility of few versus many evolutionary paths to a given robustness phenotype. This cross-disciplinary collaboration will pioneer a new strategy to discover the nature — and limits — of cellular buffering abilities that underlie extreme phenotypes and reveal the "rules" whereby mammalian cells cope with environmental variation.This project is funded by the Understanding the Rules of Life: Epigenetics Program, administered as part of NSF's Ten Big Ideas through the Division of Emerging Frontiers in the Directorate for Biological Sciences.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.
期刊论文(3)
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会议论文
RAPID: Comparative genomics of SARS-CoV-2 susceptibility and immune defense in mammals
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
Cell Research
Cell Research (细胞研究)