R01MH134809
Project Grant
Overview
Grant Description
Cellular resolution multi-omics of white matter tracts in developing human and non-human primate brain for cell atlases - project summary/abstract. The molecular evolution underlying cell type diversity and function has facilitated the increased cognitive capacity of humans. While significant progress has been made to uncover cell type specific gene expression programs in the brains of rodents, only a modest amount of progress has been made in human brains. Moreover, the majority of the existing cell type genomic datasets focus on gray matter.
Our recent work has identified important human-specific gene expression patterns relevant to non-neurons, especially oligodendrocytes. Human brain imaging studies in disorders such as autism spectrum disorders and schizophrenia have identified alterations in white matter tracts that are primarily comprised of oligodendrocytes. We therefore propose to profile white matter tracts that are anatomically comparable across primates: pyramidal tract, optic chiasm, cerebellar white matter, and corpus callosum.
Because oligodendrocyte maturation varies between gray and white matter, we will profile tissue across development. This comparative cell type profiling between human and non-human primate brain will provide spatially defined epigenomic and transcriptomic data through the following four aims: 1) profile single cell level transcriptional maps and chromatin states of white matter tracts and functionally associated gray matter in human brain across development; 2) profile single cell level transcriptional maps and chromatin states of white matter tracts and functionally associated gray matter across development in two non-human primates: rhesus macaque and the common marmoset; 3) profile single cell level transcriptional maps and chromatin states of white matter tracts and functionally associated gray matter in additional tissue from adult great ape and monkey brains; and 4) validate observed differences in white matter composition at the cell type level in human and non-human primates.
Together, these aims will molecularly define understudied cell types from human and non-human primate brains.
Our recent work has identified important human-specific gene expression patterns relevant to non-neurons, especially oligodendrocytes. Human brain imaging studies in disorders such as autism spectrum disorders and schizophrenia have identified alterations in white matter tracts that are primarily comprised of oligodendrocytes. We therefore propose to profile white matter tracts that are anatomically comparable across primates: pyramidal tract, optic chiasm, cerebellar white matter, and corpus callosum.
Because oligodendrocyte maturation varies between gray and white matter, we will profile tissue across development. This comparative cell type profiling between human and non-human primate brain will provide spatially defined epigenomic and transcriptomic data through the following four aims: 1) profile single cell level transcriptional maps and chromatin states of white matter tracts and functionally associated gray matter in human brain across development; 2) profile single cell level transcriptional maps and chromatin states of white matter tracts and functionally associated gray matter across development in two non-human primates: rhesus macaque and the common marmoset; 3) profile single cell level transcriptional maps and chromatin states of white matter tracts and functionally associated gray matter in additional tissue from adult great ape and monkey brains; and 4) validate observed differences in white matter composition at the cell type level in human and non-human primates.
Together, these aims will molecularly define understudied cell types from human and non-human primate brains.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Dallas,
Texas
753907208
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 168% from $1,570,076 to $4,203,209.
The University Of Texas Southwestern Medical Center was awarded
Cellular Multi-Omics of White Matter Tracts in Human & Primate Brain
Project Grant R01MH134809
worth $4,203,209
from the National Institute of Mental Health in May 2024 with work to be completed primarily in Dallas Texas United States.
The grant
has a duration of 2 years 9 months and
was awarded through assistance program 93.242 Mental Health Research Grants.
The Project Grant was awarded through grant opportunity BRAIN Initiative Cell Atlas Network (BICAN): Specialized Collaboratory on Human, Non-human Primate, and Mouse Brain Cell Atlases (R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 6/5/26
Period of Performance
5/1/24
Start Date
2/28/27
End Date
Funding Split
$4.2M
Federal Obligation
$0.0
Non-Federal Obligation
$4.2M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01MH134809
Transaction History
Modifications to R01MH134809
Additional Detail
Award ID FAIN
R01MH134809
SAI Number
R01MH134809-787702358
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75N700 NIH National Institute of Mental Health
Funding Office
75N700 NIH National Institute of Mental Health
Awardee UEI
YZJ6DKPM4W63
Awardee CAGE
1CNP4
Performance District
TX-30
Senators
John Cornyn
Ted Cruz
Ted Cruz
Modified: 6/5/26