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Series GSE186346 Query DataSets for GSE186346
Status Public on Feb 10, 2023
Title Extensive sex differences in depression-linked variants functionally assayed in mouse brain [Hippocampus]
Organisms Mus musculus; Adeno-associated virus 9
Experiment type Expression profiling by high throughput sequencing
Other
Summary Here, we selected >1000 variants from over 30 depression-associated loci using brain epigenomic data, and functionally assayed them using in vivo functional assays in the mouse brain to examine sex-by-genotype interactions. We identify extensive sex-by-allele effects in mature hippocampus, suggesting genetic risk and thus disease mechanisms may be distinct between the sexes. Unbiased informatics approaches indicated a role for nuclear hormone receptors, which was supported by . Further, comparative analysis of allelic function in the neonatal mouse brain, during a key between developmental neonates during the masculinizing testosterone surge, and in the adult hippocampus—a region of interest in depression pathology—but not at 10 days old, a older hormonally quiescent developmental stage juveniles. Our study provides novel insights into depression genetics as influenced by age, biological sex, and cell type, and provides a framework for in vivo parallel assays at a scale not previously shown possible to functionally define interactions between sex and disease variation.
 
Overall design n=5 replicates each of AAV9-transduced adult mouse brain tissues: male total hippocampus, female total hippocampus, male Vglut1+ translating-ribosome affinity purification immunoprecipitated RNA fraction, female Vglut1+ translating-ribosome affinity purification immunoprecipitated RNA fraction.

Additional grant information: 571009 - Joseph Dougherty - Simons Foundation
 
Contributor(s) Mulvey B, Dougherty JD, Selmanovic D
Citation(s) 36803612
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 MH116999 Highly parallel analysis of 5' and 3' UTR variants in Autism Spectrum Disorders WASHINGTON UNIVERSITY JOSEPH D DOUGHERTY
F30 MH116654 Identification and characterization of common, noncoding regulatory variants associated with Major Depressive Disorder. WASHINGTON UNIVERSITY Bernard John Mulvey
Submission date Oct 21, 2021
Last update date May 12, 2023
Contact name Joseph Dougherty
E-mail(s) mulveyb@wustl.edu, jdougherty@wustl.edu, berniejmulvey@gmail.com
Organization name Washington University in St. Louis
Department Genetics
Lab Dougherty
Street address 660 S Euclid Ave, Campus Box 8232
City St. Louis
State/province MO
ZIP/Postal code 63110
Country USA
 
Platforms (2)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
GPL30885 Illumina NovaSeq 6000 (Adeno-associated virus 9)
Samples (25)
GSM5645922 AAV9_Lysate_TechRep1
GSM5645923 AAV9_Lysate_TechRep2
GSM5645924 AAV9_Lysate_TechRep3
This SubSeries is part of SuperSeries:
GSE186348 Extensive sex differences in depression-linked variants functionally assayed in mouse brain
Relations
BioProject PRJNA773474
SRA SRP342576

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE186346_Reference-Barcode_Sequences__their_paired_internal_identifiers__and_the_corresponding_sequence_placed_upstream_of_min_promoter.txt.gz 1.3 Mb (ftp)(http) TXT
GSE186346_Unfiltered_Barcode_Counts-Hippocampal_TRAP_MPRA.txt.gz 1.4 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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