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Series GSE13257 Query DataSets for GSE13257
Status Public on Oct 18, 2008
Title Analysis of Genes in the Hypothalamus Controlling Feed Intake and Energy Metabolism in Neonatal Chicks
Organism Gallus gallus
Experiment type Expression profiling by array
Summary Delayed access to feed following hatching has been associated with reduction in growth performance in chicks. However, the gene networks within the hypothalamus that regulate feed intake and metabolism, and the effects of fasting on those pathways are not well understood. The present experiment evaluated global hypothalamic gene expression in neonatal chicks using the Arizona Gallus gallus 20.7K Oligo Array v1.0 to elucidate genes and pathways regulated by feeding, fasting, and refeeding. Ten groups of chicks were sampled over four days post-hatch, including: control (at hatch), 24h fed, 24h fasted, 48h fed, 48h fasted, 48h fasted then 4h refed, 72h fed, 48h fasted then 24h refed, 96h fed, and 48h fasted then 48h refed. Non-esterified fatty acids were elevated, and triglycerides were decreased in fasted chicks at 24 and 48h, indicating that fasting induced physiological changes. Hypothalamic samples were collected from 16 chicks per group, and total RNA was extracted and pooled for hybridization (n=4). Expression patterns of selected genes were confirmed by quantitative real-time PCR. Two-fold differences in gene expression were detected in 1,272 genes between treatment groups, and of those, 119 genes were significantly (P<0.05) different. Assignment of gene ontology terms to the significant genes resulted in 34 different categories of biological processes, with 24% of genes participating in signal transduction, transport, or metabolic processes. Genes that were upregulated during fasting (and confirmed by qPCR) include FK506BP51, which is involved in the formation of steroid receptor complexes, and deiodinase type II, which is responsible for converting the thyroid hormone T4 into T3. Confirmed genes, downregulated due to fasting, included proopiomelanocortin and fatty acid binding protein 7. Other regulated genes were identified that play a role in feeding and obesity in other species, such as relaxin 3 and adrenergic receptor-β2. Further analysis of differentially regulated genes could provide new information regarding the role of the hypothalamus in feed intake and metabolism.

Keywords: Metabolic perturbation
 
Overall design Ten experimental groups with 4 replicates each were analyzed. A reference RNA design was used for this microarray. Equal amounts of amplified RNA (aRNA) from all samples were pooled and labeled with the Alexa 647 to create the reference pool. Each individual sample was labeled with Alexa 555. Each slide was hybridized with both the reference pool and one sample.
 
Contributor(s) Porter TE, Higgins SE
Citation(s) 20214824
Submission date Oct 17, 2008
Last update date Jan 18, 2013
Contact name Tom E. Porter
E-mail(s) teporter@umd.edu
Phone 301 405 2516
Organization name University of Maryland
Department Animal and Avian Sciences
Street address Building 142
City College Park
State/province MD
ZIP/Postal code 20742
Country USA
 
Platforms (1)
GPL6049 Arizona Gallus gallus 20.7K Oligo Array v1.0
Samples (40)
GSM334675 Hypothalamus, Day-of-hatch chick, Replicate 1
GSM334676 Hypothalamus, Day-of-hatch chick, Replicate 2
GSM334677 Hypothalamus, Day-of-hatch chick, Replicate 3
Relations
BioProject PRJNA109541

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
GSE13257.txt 3.2 Mb (ftp)(http) TXT
GSE13257_RAW.tar 62.9 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table
Processed data are available on Series record

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