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Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism
Estrogens are traditionally considered to be female sex steroid hormones and most of the studies examining estrogen regulation of metabolic function in the liver have been conducted in females. However, the liver expresses high levels of estrogen receptor alpha (ESR1) in both males and females, whic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330359/ https://www.ncbi.nlm.nih.gov/pubmed/30671521 http://dx.doi.org/10.1016/j.dib.2018.12.089 |
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author | Khristi, Vincentaben Ratri, Anamika Ghosh, Subhra Borosha, Shaon Dai, Eddie Chakravarthi, V. Praveen Rumi, M.A. Karim Wolfe, Michael W. |
author_facet | Khristi, Vincentaben Ratri, Anamika Ghosh, Subhra Borosha, Shaon Dai, Eddie Chakravarthi, V. Praveen Rumi, M.A. Karim Wolfe, Michael W. |
author_sort | Khristi, Vincentaben |
collection | PubMed |
description | Estrogens are traditionally considered to be female sex steroid hormones and most of the studies examining estrogen regulation of metabolic function in the liver have been conducted in females. However, the liver expresses high levels of estrogen receptor alpha (ESR1) in both males and females, which mediates the hepatic response to estrogens. In this data article, we investigated whether metabolic disorders in Esr1 knockout (Esr1-/-) male rats were linked with loss of transcriptional regulation by ESR1 in liver. To identify the ESR1 regulated genes in the mutant liver, RNA-sequencing was performed on liver RNAs purified from young male rats. The raw data were analyzed using the CLC Genomics Workbench and high-quality RNA-sequencing reads were aligned to the Rattus norvegicus genome. Transcriptome data obtained from Esr1-/- liver RNAs were compared to that of wild type rats. Based on an absolute fold change of 2 with a p-value ≤ 0.05, a total of 618 differentially expressed genes were identified in the Esr1-/- male liver. Pathway analyses demonstrated that the majority of differentially expressed genes are regulators of carbohydrate and lipid metabolism in the liver. These differentially expressed genes and their potential roles were further examined in a companion manuscript, “Disruption of ESR1 alters the expression of genes regulating hepatic lipid and carbohydrate metabolism in male rats” (Khristi et al., 2018). |
format | Online Article Text |
id | pubmed-6330359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-63303592019-01-22 Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism Khristi, Vincentaben Ratri, Anamika Ghosh, Subhra Borosha, Shaon Dai, Eddie Chakravarthi, V. Praveen Rumi, M.A. Karim Wolfe, Michael W. Data Brief Biochemistry, Genetics and Molecular Biology Estrogens are traditionally considered to be female sex steroid hormones and most of the studies examining estrogen regulation of metabolic function in the liver have been conducted in females. However, the liver expresses high levels of estrogen receptor alpha (ESR1) in both males and females, which mediates the hepatic response to estrogens. In this data article, we investigated whether metabolic disorders in Esr1 knockout (Esr1-/-) male rats were linked with loss of transcriptional regulation by ESR1 in liver. To identify the ESR1 regulated genes in the mutant liver, RNA-sequencing was performed on liver RNAs purified from young male rats. The raw data were analyzed using the CLC Genomics Workbench and high-quality RNA-sequencing reads were aligned to the Rattus norvegicus genome. Transcriptome data obtained from Esr1-/- liver RNAs were compared to that of wild type rats. Based on an absolute fold change of 2 with a p-value ≤ 0.05, a total of 618 differentially expressed genes were identified in the Esr1-/- male liver. Pathway analyses demonstrated that the majority of differentially expressed genes are regulators of carbohydrate and lipid metabolism in the liver. These differentially expressed genes and their potential roles were further examined in a companion manuscript, “Disruption of ESR1 alters the expression of genes regulating hepatic lipid and carbohydrate metabolism in male rats” (Khristi et al., 2018). Elsevier 2019-01-04 /pmc/articles/PMC6330359/ /pubmed/30671521 http://dx.doi.org/10.1016/j.dib.2018.12.089 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Biochemistry, Genetics and Molecular Biology Khristi, Vincentaben Ratri, Anamika Ghosh, Subhra Borosha, Shaon Dai, Eddie Chakravarthi, V. Praveen Rumi, M.A. Karim Wolfe, Michael W. Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
title | Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
title_full | Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
title_fullStr | Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
title_full_unstemmed | Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
title_short | Liver transcriptome data of Esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
title_sort | liver transcriptome data of esr1 knockout male rats reveals altered expression of genes involved in carbohydrate and lipid metabolism |
topic | Biochemistry, Genetics and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330359/ https://www.ncbi.nlm.nih.gov/pubmed/30671521 http://dx.doi.org/10.1016/j.dib.2018.12.089 |
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