In vivo tracking of bioluminescent markers of circadian rhythms in behaving animals

Information

  • Research Project
  • 9880719
  • ApplicationId
    9880719
  • Core Project Number
    R15GM126545
  • Full Project Number
    2R15GM126545-02A1
  • Serial Number
    126545
  • FOA Number
    PAR-18-714
  • Sub Project Id
  • Project Start Date
    9/15/2017 - 7 years ago
  • Project End Date
    9/17/2022 - 2 years ago
  • Program Officer Name
    SESMA, MICHAEL A
  • Budget Start Date
    9/18/2019 - 5 years ago
  • Budget End Date
    9/17/2022 - 2 years ago
  • Fiscal Year
    2019
  • Support Year
    02
  • Suffix
    A1
  • Award Notice Date
    9/18/2019 - 5 years ago
Organizations

In vivo tracking of bioluminescent markers of circadian rhythms in behaving animals

Project Summary Circadian rhythm disruption, as experienced in shift work, nocturnal light exposure, and aging, is a serious risk factor for disease, including cancer, diabetes, obesity, and cardiovascular and neurodegenerative diseases. As we learn more about the circadian system, it is becoming clear that these disruptions arise not only from shifts in the clocks of individual organs, but also from disruptions of the complex interactions among the clocks of different organs. To study these interactions at a system level, we have developed a method to measure circadian rhythms in specific organs of living animals. We will apply this method to address a fundamental unresolved question in the application of chronobiology to health: By what method can we optimize entrainment of the entire circadian system to shifted light signals? Using our method of in vivo, molecular, organ-specific detection of rhythm in behaving animals, we will search for new methods of resetting the clock that maintain phase alignment among clock components. In parallel, we will continue to develop new approaches for the study of circadian rhythm dynamics in vivo. Our first aim is to measure the entrainment dynamics of liver and brain suprachiasmatic nuclei (SCN) in response to an advanced light cycle. We will then determine if timed food availability can serve to shift the liver faster so that is does not lag behind the shift of the SCN. Undergraduate students at the largest US women's college, Smith College, will conduct this research. Through a multifaceted program with documented success, we will recruit 1st-year students from under-represented minority groups and engage them in hands-on scientific research, with engaged mentorship. Student research teams will include majors with strong quantitative training (e.g., statistics and data science, engineering) and results will be shared via our lab site on the Open Science Framework. Students will be involved in all aspects of the research and will present results at conferences and contribute to publications.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R15
  • Administering IC
    GM
  • Application Type
    2
  • Direct Cost Amount
    300000
  • Indirect Cost Amount
    92394
  • Total Cost
    392394
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:392394\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    SMITH COLLEGE
  • Organization Department
    NEUROSCIENCES
  • Organization DUNS
    066989427
  • Organization City
    NORTHAMPTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    010636304
  • Organization District
    UNITED STATES