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Identification of microRNA that represses IRS-1 expression in liver

MicroRNAs (miRNAs) are short, non-coding RNAs that post-transcriptionally regulate gene expression and have been shown to participate in almost every cellular process. Several miRNAs have recently been implicated in glucose metabolism, but the roles of miRNAs in insulin-resistant conditions, such as...

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Autores principales: Ono, Kaoru, Igata, Motoyuki, Kondo, Tatsuya, Kitano, Sayaka, Takaki, Yuki, Hanatani, Satoko, Sakaguchi, Masaji, Goto, Rieko, Senokuchi, Takafumi, Kawashima, Junji, Furukawa, Noboru, Motoshima, Hiroyuki, Araki, Eiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783395/
https://www.ncbi.nlm.nih.gov/pubmed/29364977
http://dx.doi.org/10.1371/journal.pone.0191553
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author Ono, Kaoru
Igata, Motoyuki
Kondo, Tatsuya
Kitano, Sayaka
Takaki, Yuki
Hanatani, Satoko
Sakaguchi, Masaji
Goto, Rieko
Senokuchi, Takafumi
Kawashima, Junji
Furukawa, Noboru
Motoshima, Hiroyuki
Araki, Eiichi
author_facet Ono, Kaoru
Igata, Motoyuki
Kondo, Tatsuya
Kitano, Sayaka
Takaki, Yuki
Hanatani, Satoko
Sakaguchi, Masaji
Goto, Rieko
Senokuchi, Takafumi
Kawashima, Junji
Furukawa, Noboru
Motoshima, Hiroyuki
Araki, Eiichi
author_sort Ono, Kaoru
collection PubMed
description MicroRNAs (miRNAs) are short, non-coding RNAs that post-transcriptionally regulate gene expression and have been shown to participate in almost every cellular process. Several miRNAs have recently been implicated in glucose metabolism, but the roles of miRNAs in insulin-resistant conditions, such as obesity or type 2 diabetes, are largely unknown. Herein, we focused on miR-222, the expression of which was increased in the livers of high fat/high sucrose diet-fed mice injected with gold thioglucose (G+HFHSD). Overexpression of miR-222 in primary mouse hepatocytes attenuated Akt phosphorylation induced by insulin, indicating that miR-222 negatively regulates insulin signaling. As per in silico analysis, miR-222 potentially binds to the 3′ untranslated region (3′ UTR) of the IRS-1 gene, a key insulin signaling molecule. In fact, IRS-1 protein expression was decreased in the livers of G+HFHSD-fed mice. We further confirmed a direct interaction between miR-222 and the 3′ UTR of IRS-1 via luciferase assays. Our findings suggest that up-regulation of miR-222 followed by reduction in IRS-1 expression may be a viable mechanism of insulin resistance in the liver.
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spelling pubmed-57833952018-02-08 Identification of microRNA that represses IRS-1 expression in liver Ono, Kaoru Igata, Motoyuki Kondo, Tatsuya Kitano, Sayaka Takaki, Yuki Hanatani, Satoko Sakaguchi, Masaji Goto, Rieko Senokuchi, Takafumi Kawashima, Junji Furukawa, Noboru Motoshima, Hiroyuki Araki, Eiichi PLoS One Research Article MicroRNAs (miRNAs) are short, non-coding RNAs that post-transcriptionally regulate gene expression and have been shown to participate in almost every cellular process. Several miRNAs have recently been implicated in glucose metabolism, but the roles of miRNAs in insulin-resistant conditions, such as obesity or type 2 diabetes, are largely unknown. Herein, we focused on miR-222, the expression of which was increased in the livers of high fat/high sucrose diet-fed mice injected with gold thioglucose (G+HFHSD). Overexpression of miR-222 in primary mouse hepatocytes attenuated Akt phosphorylation induced by insulin, indicating that miR-222 negatively regulates insulin signaling. As per in silico analysis, miR-222 potentially binds to the 3′ untranslated region (3′ UTR) of the IRS-1 gene, a key insulin signaling molecule. In fact, IRS-1 protein expression was decreased in the livers of G+HFHSD-fed mice. We further confirmed a direct interaction between miR-222 and the 3′ UTR of IRS-1 via luciferase assays. Our findings suggest that up-regulation of miR-222 followed by reduction in IRS-1 expression may be a viable mechanism of insulin resistance in the liver. Public Library of Science 2018-01-24 /pmc/articles/PMC5783395/ /pubmed/29364977 http://dx.doi.org/10.1371/journal.pone.0191553 Text en © 2018 Ono et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ono, Kaoru
Igata, Motoyuki
Kondo, Tatsuya
Kitano, Sayaka
Takaki, Yuki
Hanatani, Satoko
Sakaguchi, Masaji
Goto, Rieko
Senokuchi, Takafumi
Kawashima, Junji
Furukawa, Noboru
Motoshima, Hiroyuki
Araki, Eiichi
Identification of microRNA that represses IRS-1 expression in liver
title Identification of microRNA that represses IRS-1 expression in liver
title_full Identification of microRNA that represses IRS-1 expression in liver
title_fullStr Identification of microRNA that represses IRS-1 expression in liver
title_full_unstemmed Identification of microRNA that represses IRS-1 expression in liver
title_short Identification of microRNA that represses IRS-1 expression in liver
title_sort identification of microrna that represses irs-1 expression in liver
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783395/
https://www.ncbi.nlm.nih.gov/pubmed/29364977
http://dx.doi.org/10.1371/journal.pone.0191553
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