Skip directly to content

Minimize RSR Award Detail

Research Spending & Results

Award Detail

Awardee:BOARD OF REGENTS NEVADA SYSTEM OF HIGHER EDUCATION
Doing Business As Name:University of Nevada Las Vegas
PD/PI:
  • Allyson Hindle
  • (702) 895-3104
  • allyson.hindle@unlv.edu
Award Date:07/06/2020
Estimated Total Award Amount: $ 884,080
Funds Obligated to Date: $ 884,080
  • FY 2020=$884,080
Start Date:09/01/2020
End Date:08/31/2025
Transaction Type:Grant
Agency:NSF
Awarding Agency Code:4900
Funding Agency Code:4900
CFDA Number:47.074
Primary Program Source:040100 NSF RESEARCH & RELATED ACTIVIT
Award Title or Description:Collaborative Research: URoL:Epigenetics 2: Epigenetic pathways to regulate homeostatic resilience: Model-based discovery of rules across diverse mammals
Federal Award ID Number:2022046
DUNS ID:098377336
Parent DUNS ID:067808063
Program:URoL-Understanding the Rules o
Program Officer:
  • Rebecca Ferrell
  • (703) 292-7850
  • rferrell@nsf.gov

Awardee Location

Street:4505 MARYLAND PARKWAY
City:Las Vegas
State:NV
ZIP:89154-9900
County:Las Vegas
Country:US
Awardee Cong. District:01

Primary Place of Performance

Organization Name:University of Nevada Las Vegas
Street:
City:
State:NV
ZIP:89154-1055
County:Las Vegas
Country:US
Cong. District:01

Abstract at Time of Award

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.

For specific questions or comments about this information including the NSF Project Outcomes Report, contact us.