In this project we will bridge the traditionally largely distinct fields of quantitative genetics and mechanistic biology to obtain a mechanistic understanding of regulatory effects of genetic variants in humans. Leveraging on large human data sets providing parallel whole genome and transcriptome sequencing data, we will extend proof-of-principle studies and computational approaches developed and validated in model organisms to achieve improved functional interpretation of GWAS loci associated to mental health disorders. We focus specifically on the role of transcription factors as both upstream regulators of genetic risk variants as well as mediators of downstream network-level effects.
As Aim 1, we will develop extend methods to allow accurate modeling of transcription factor activity from transcriptome data from large cohorts of human tissue samples in GTEx, PsychENCODE, and TOPMed cohorts. These data will be used in Aim 2 to dissect the mechanisms underlying proximal genetic regulatory variants in cis. We hypothesize that dynamics of transcription factor activity and binding modifies the effect size of genetic regulatory variants across individuals, tissues, and cell types, and that by modeling this relationship we can detect TFs regulating specific regulatory variants and noncoding disease-associated loci. In parallel Aim 3, we will map network-level trans-acting genetic variants for inter-individual variation in TF activity. Going beyond treating TF activity as a tissue-specific parameter of the cellular environment, we will now consider it as a variable quantitative trait itself, and by GWAS/TWAS for inferred TF activity, we map specific polymorphisms that affect TF activity within each tissue. We anticipate that the trans-acting loci discovered in this analysis will be of major interest not only to basic biology of regulatory networks, but also for explaining GWAS associations to complex diseases, and to mental health in particular.

Public Health Relevance

Population genomics allows us to map the genetic determinants of human disease, but keeps the underlying molecular mechanisms and pathways hidden. Functional genomics, on the other hand, allow researchers to dissect the molecular machinery of the cell that interprets the instructions hidden in our genome, but does not provide explicit connections to disease. In this project, we develop computational strategies that exploit existing knowledge about molecular networks to achieve mechanistic understanding of how genetic variants impact disease, which can help suggest specific therapeutic directions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH106842-05
Application #
10067570
Study Section
Genomics, Computational Biology and Technology Study Section (GCAT)
Program Officer
Arguello, Alexander
Project Start
2015-04-01
Project End
2024-10-31
Budget Start
2020-11-01
Budget End
2021-10-31
Support Year
5
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Biochemistry
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Castel, Stephane E; Cervera, Alejandra; Mohammadi, Pejman et al. (2018) Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk. Nat Genet 50:1327-1334
Kim-Hellmuth, Sarah; Bechheim, Matthias; Pütz, Benno et al. (2017) Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. Nat Commun 8:266
Mohammadi, Pejman; Castel, Stephane E; Brown, Andrew A et al. (2017) Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change. Genome Res 27:1872-1884
GTEx Consortium; Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group; Statistical Methods groups—Analysis Working Group et al. (2017) Genetic effects on gene expression across human tissues. Nature 550:204-213
Pickrell, Joseph K; Berisa, Tomaz; Liu, Jimmy Z et al. (2016) Detection and interpretation of shared genetic influences on 42 human traits. Nat Genet 48:709-17
Castel, Stephane E; Mohammadi, Pejman; Chung, Wendy K et al. (2016) Rare variant phasing and haplotypic expression from RNA sequencing with phASER. Nat Commun 7:12817
Kim-Hellmuth, Sarah; Lappalainen, Tuuli (2016) Concerted Genetic Function in Blood Traits. Cell 167:1167-1169
Berisa, Tomaz; Pickrell, Joseph K (2016) Approximately independent linkage disequilibrium blocks in human populations. Bioinformatics 32:283-5