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Published on: November 29, 2013
Next-Generation Sequencing Identifies Polyunsaturated Fatty Acid Responsive Genes in the Juvenile Rat Cerebellum
Aaron A Mehus1, Aaron M Dickey2, Timothy P L Smith3
1USDA-ARS Grand Forks Human Nutrition Research Center, Grand Forks, ND 58203, USA. Aaron.Mehus@ARS.USDA.GOV.
Insights
Depleting dietary omega-3 polyunsaturated fatty acids (PUFA) in juvenile rats altered cerebellar fatty acid profiles and gene expression. Specifically, the gene Nr4a3, important for neuroprotection, was upregulated in rats fed an omega-3 deficient diet.
Area of Science:
- Neuroscience
- Nutritional Science
- Molecular Biology
Background:
- Dietary omega-3 polyunsaturated fatty acids (PUFA) are crucial for brain development.
- Limited data exist on the impact of omega-3 PUFA during the juvenile period post-weaning, a critical growth phase.
- Understanding these effects is vital for optimizing brain health during development.
Purpose of the Study:
- To investigate the effects of dietary omega-3 PUFA depletion on the juvenile rat cerebellum.
- To identify specific gene expression changes in the cerebellum in response to altered omega-3 PUFA intake.
- To test the hypothesis that omega-3 PUFA deficiency modifies the cerebellar transcriptome.
Main Methods:
- Juvenile male rats were fed either an omega-3 sufficient (soybean oil) or deficient (corn oil) diet for four weeks.
- Cerebellar fatty acid composition was analyzed.
- Differential gene expression analysis was performed using RNA sequencing and two normalization methods (UQ scaling, TPM).
Main Results:
- Omega-3 deficient diet increased cerebellar n-6 fatty acids (DPA, AA, DTA) but did not decrease DHA.
- Transcriptome analysis identified differentially expressed genes (DEGs) between the diets.
- The gene Nr4a3, involved in neuroprotection and learning, showed a >2-fold increase in expression in the omega-3 deficient group.
Conclusions:
- Dietary omega-3 PUFA levels significantly influence the juvenile rat cerebellar transcriptome.
- Cerebellar Nr4a3 gene expression is responsive to dietary omega-3 PUFA.
- Further research is needed to elucidate the neurodevelopmental implications of omega-3 PUFA and Nr4a3 interactions.
Abstract:
Dietary n-3 polyunsaturated fatty acids (PUFA) influence postnatal brain growth and development. However, little data exist regarding the impacts of dietary n-3 PUFA in juvenile animals post weaning, which is a time of rapid growth. We tested the hypothesis that depleting dietary n-3 PUFA would result in modifications to the cerebellar transcriptome of juvenile rats. To test this hypothesis, three week old male rats (an age that roughly corresponds to an 11 month old child in brain development) were fed diets containing either soybean oil (SO) providing 1.1% energy from α-linolenic acid (ALA; 18:3n-3; ALA-sufficient) or corn oil (CO) providing 0.13% energy from ALA (ALA-deficient) for four weeks. Fatty acids (FAs) in the cerebellum were analyzed and revealed a 4-fold increase in n-6 docosapentaenoic acid (DPA; 22:5n-6), increases in arachidonic acid (AA; 20:4n-6) and docosatetraenoic acid (DTA; 22:4n-6), but no decrease in docosahexaenoic acid (DHA; 22:6n-3), in animals fed CO versus SO. Transcript abundance was then characterized to identify differentially expressed genes (DEGs) between the two diets. Upper quartile (UQ) scaling and transcripts per million (TPM) data normalization identified 100 and 107 DEGs, respectively. Comparison of DEGs from the two normalization methods identified 70 genes that overlapped, with 90% having abundance differences less than 2-fold. Nr4a3, a transcriptional activator that plays roles in neuroprotection and learning, was elevated over 2-fold from the CO diet. These data indicate that expression of Nr4a3 in the juvenile rat cerebellum is responsive to dietary n-3 PUFA, but additional studies are needed clarify the neurodevelopmental relationships between n-3 PUFA and Nr4a3 and the resulting impacts.
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