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RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice

Growing evidence demonstrates the epigenetic modulation as a key event in Alzheimer's disease (AD) pathology. Furthermore, recent data suggests that the epigenetic regulation by the methyltransferase G9a is a crucial mechanism involved in learning and memory formation. Taking this into account,...

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Detalles Bibliográficos
Autores principales: Pawar, Shrikant, Bellver-Sanchis, Aina, Griñán-Ferré, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257974/
https://www.ncbi.nlm.nih.gov/pubmed/34307805
http://dx.doi.org/10.1016/j.dib.2021.107114
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author Pawar, Shrikant
Bellver-Sanchis, Aina
Griñán-Ferré, Christian
author_facet Pawar, Shrikant
Bellver-Sanchis, Aina
Griñán-Ferré, Christian
author_sort Pawar, Shrikant
collection PubMed
description Growing evidence demonstrates the epigenetic modulation as a key event in Alzheimer's disease (AD) pathology. Furthermore, recent data suggests that the epigenetic regulation by the methyltransferase G9a is a crucial mechanism involved in learning and memory formation. Taking this into account, we hereby provide genomics data from pharmacological intervention with UNC0642, a potent and selective G9a/GLP in SAMP8 mice, a model of Alzheimer's disease (AD). We have generated novel RNA-seq and miRNA-seq data for three groups, healthy SAMR1, SAMP8 control and SAMP8 treated with UNC0642 (5 mg/Kg). Thus, the new data can be used to find miRNA regulation, and the mRNA's modified in AD under G9a/GLP inhibition.
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spelling pubmed-82579742021-07-23 RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice Pawar, Shrikant Bellver-Sanchis, Aina Griñán-Ferré, Christian Data Brief Data Article Growing evidence demonstrates the epigenetic modulation as a key event in Alzheimer's disease (AD) pathology. Furthermore, recent data suggests that the epigenetic regulation by the methyltransferase G9a is a crucial mechanism involved in learning and memory formation. Taking this into account, we hereby provide genomics data from pharmacological intervention with UNC0642, a potent and selective G9a/GLP in SAMP8 mice, a model of Alzheimer's disease (AD). We have generated novel RNA-seq and miRNA-seq data for three groups, healthy SAMR1, SAMP8 control and SAMP8 treated with UNC0642 (5 mg/Kg). Thus, the new data can be used to find miRNA regulation, and the mRNA's modified in AD under G9a/GLP inhibition. Elsevier 2021-05-02 /pmc/articles/PMC8257974/ /pubmed/34307805 http://dx.doi.org/10.1016/j.dib.2021.107114 Text en © 2021 Published by Elsevier Inc. https://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 Data Article
Pawar, Shrikant
Bellver-Sanchis, Aina
Griñán-Ferré, Christian
RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice
title RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice
title_full RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice
title_fullStr RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice
title_full_unstemmed RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice
title_short RNA-seq and miRNA-seq data from pharmacological inhibition of the G9a/GLP histone methyltransferase complex with UNC0642 in SAMP8 mice
title_sort rna-seq and mirna-seq data from pharmacological inhibition of the g9a/glp histone methyltransferase complex with unc0642 in samp8 mice
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257974/
https://www.ncbi.nlm.nih.gov/pubmed/34307805
http://dx.doi.org/10.1016/j.dib.2021.107114
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