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Series GSE149828 Query DataSets for GSE149828
Status Public on May 05, 2020
Title Developmental Alterations in the Transcriptome of Three Distinct Rodent Models of Schizophrenia
Organism Rattus norvegicus
Experiment type Expression profiling by high throughput sequencing
Summary Schizophrenia is a debilitating disorder affecting just under 1% of the population. While the symptoms of this disorder do not appear until late adolescence, pathological alterations likely occur earlier, during development in utero. While there is an increasing literature examining transcriptome alterations in patients, it is not possible to examine the changes in gene expression that occur during development in humans that will develop schizophrenia. Here we utilize three distinct rodent developmental disruption models of schizophrenia to examine potential overlapping alterations in the transcriptome, with a specific focus on markers of interneuron development. Specifically, we administered either methylazoxymethanol acetate (MAM), Polyinosinic:polycytidylic acid (Poly I:C), or chronic protein malnutrition, on GD 17 and examined mRNA expression in the developing hippocampus of the offspring 18 hours later. Here, we report alterations in gene expression that may contribute to the pathophysiology of schizophrenia, including significant alterations in interneuron development and ribosome function.
 
Overall design Timed pregnant female Sprague-Dawley rats were obtained from Envigo on gestational day 11. Either polyinosine:cytosine (Poly I:C, 7.5 mg/kg, i.p), methylazoxymethanol acetate (MAM: 22mg/kg, i.p.) or saline were administered on gestational day 17. For maternal protein malnutrition, pregnant rats had access to a low protein diet ad libitum (Envigo: TD.90016) containing 6.1% protein, 75.6% carbohydrate and 5.5% fat (3.8Kcal/g) from GD11-GD18. Control rats were fed an isocaloric diet of 20.3% protein, 61.6% carbohydrate and 5.5% fat (3.8Kcal/g: Envigo: TD.91352) from GD11-GD18. Experiments included three pups from multiple (two) litters for a total of 6 pups per group.
 
Contributor(s) Donegan JJ, Boley AM, Glenn JP, Carless MA, Lodge DJ
Citation(s) 32497066
Submission date May 04, 2020
Last update date Aug 04, 2020
Contact name Daniel J Lodge
E-mail(s) Lodged@uthscsa.edu
Organization name UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANTONIO
Department Pharmacology
Street address 7703 Floyd Curl Drive
City San Antonio
State/province Bexar
ZIP/Postal code 78229-3900
Country USA
 
Platforms (1)
GPL18694 Illumina HiSeq 2500 (Rattus norvegicus)
Samples (24)
GSM4513749 Low Protein 1.1
GSM4513750 Low Protein 1.2
GSM4513751 Low Protein 1.3
Relations
BioProject PRJNA630235
SRA SRP260019

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
GSE149828_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE149828_differential_expression.xlsx 506.8 Kb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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