RF1MH126723
Project Grant
Overview
Grant Description
Molecular Recording to Predict Cell Fate Decisions and Animal Behavior - Abstract
The brain is remarkably complex, and our understanding of this organ is still in its infancy. Many fundamental questions about brain development and function remain.
Single cell genomics promises new ways to answer these questions, but nearly all single-cell methods share a shortcoming – cells are destroyed when their molecular states are measured. This "destruction upon observation" makes it impossible to correlate molecular events that have occurred in the past with the final outcomes. For example, if you destroy an intermediate progenitor in the brain to profile its epigenome, you have no way to know what cell fate the progenitor would have adopted. Likewise, profiling an animal after an experience is going to conflate the molecular consequences of the experience with any molecular predispositions that were there before exposure. And if you profile before the experience, you have no way of knowing the animal's outcome – e.g. if the animal would have been a learner or not. This shortcoming is inherent to nearly all existing genomic methods and impedes a wide variety of interesting analyses.
We have recently developed a platform technology, single-cell 'calling cards' (CC), that uses transposons to capture molecular events at one instant in time and then read them out at a later time with single cell resolution. We now propose to build upon this foundation to develop a robust, easy-to-use technology platform to record molecular events at single cell resolution in the mouse brain and connect them with cell fate decision, behavioral outcomes, neuronal activity profiles, and anatomical location.
We will develop a set of widely applicable reagents and methods, apply them to a series of high-impact "test cases" to demonstrate their utility, and rapidly distribute them to the broader community.
The brain is remarkably complex, and our understanding of this organ is still in its infancy. Many fundamental questions about brain development and function remain.
Single cell genomics promises new ways to answer these questions, but nearly all single-cell methods share a shortcoming – cells are destroyed when their molecular states are measured. This "destruction upon observation" makes it impossible to correlate molecular events that have occurred in the past with the final outcomes. For example, if you destroy an intermediate progenitor in the brain to profile its epigenome, you have no way to know what cell fate the progenitor would have adopted. Likewise, profiling an animal after an experience is going to conflate the molecular consequences of the experience with any molecular predispositions that were there before exposure. And if you profile before the experience, you have no way of knowing the animal's outcome – e.g. if the animal would have been a learner or not. This shortcoming is inherent to nearly all existing genomic methods and impedes a wide variety of interesting analyses.
We have recently developed a platform technology, single-cell 'calling cards' (CC), that uses transposons to capture molecular events at one instant in time and then read them out at a later time with single cell resolution. We now propose to build upon this foundation to develop a robust, easy-to-use technology platform to record molecular events at single cell resolution in the mouse brain and connect them with cell fate decision, behavioral outcomes, neuronal activity profiles, and anatomical location.
We will develop a set of widely applicable reagents and methods, apply them to a series of high-impact "test cases" to demonstrate their utility, and rapidly distribute them to the broader community.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Saint Louis,
Missouri
631101010
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 07/31/24 to 07/31/25.
Washington University was awarded
Predicting Cell Fate Decisions Animal Behavior through Molecular Recording
Project Grant RF1MH126723
worth $3,693,282
from the National Institute of Mental Health in August 2021 with work to be completed primarily in Saint Louis Missouri United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.242 Mental Health Research Grants.
The Project Grant was awarded through grant opportunity BRAIN Initiative: Development and Validation of Novel Tools to Probe Cell-Specific and Circuit-Specific Processes in the Brain (R01 Clinical Trial Not Allowed).
Status
(Complete)
Last Modified 7/19/24
Period of Performance
8/1/21
Start Date
7/31/25
End Date
Funding Split
$3.7M
Federal Obligation
$0.0
Non-Federal Obligation
$3.7M
Total Obligated
Activity Timeline
Transaction History
Modifications to RF1MH126723
Additional Detail
Award ID FAIN
RF1MH126723
SAI Number
RF1MH126723-2837280537
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75N700 NIH NATIONAL INSTITUTE OF MENTAL HEALTH
Funding Office
75N700 NIH NATIONAL INSTITUTE OF MENTAL HEALTH
Awardee UEI
L6NFUM28LQM5
Awardee CAGE
2B003
Performance District
MO-01
Senators
Joshua Hawley
Eric Schmitt
Eric Schmitt
Modified: 7/19/24