Major depression is a serious psychiatric disorder impacting the lives of millions of Americans. The gene DISC1 has been linked to this disorder by translocation in a single Scottish family as well as being supported by functional analyses of the gene prominent in neural development. We propose to carry out whole genome sequencing on 40 members of the original translocation family to identify possible variants that modify the effec of the translocation on phenotype as well as examine epigenetic differences in those that bear the translocation. We will also carry out genetic analyses by both genotyping and targeted sequencing to look for genetic differences in DISC1 and its core pathway genes in a total of nearly 10,000 people. Lastly, we will examine blood samples from some of those individuals with variants in the core pathway to determine if these variants change gene expression.

Public Health Relevance

Major depression is a significant public health problem in the U.S. and throughout the world. In an effort to better understand the mechanism of the illness we propose to analyze the genetic variation in a rare family heavily burdened by the disorder and then examine variants associated with those found in that family in a much larger set of unrelated people. Our ultimate goal is to identify variants that may be valuable to diagnose and guide treatment options for those with the disorder.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH102068-02
Application #
8722041
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Senthil, Geetha
Project Start
2013-08-16
Project End
2016-06-30
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Walker, Rosie May; Sussmann, Jessika Elizabeth; Whalley, Heather Clare et al. (2016) Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disorders. Bipolar Disord 18:410-22
Walker, Rosie May; Christoforou, Andrea Nikie; McCartney, Daniel L et al. (2016) DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder. Clin Epigenetics 8:5
Walker, Rosie May; Rybka, Joanna; Anderson, Susan Maguire et al. (2015) Preliminary investigation of miRNA expression in individuals at high familial risk of bipolar disorder. J Psychiatr Res 62:48-55
Ryan, Niamh M; Morris, Stewart W; Porteous, David J et al. (2014) SuRFing the genomics wave: an R package for prioritising SNPs by functionality. Genome Med 6:79