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In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala

The Megalobrama amblycephala (M. amblycephala) is one of the most important economic freshwater fish in China. The molecular mechanism under the glucose intolerance responses which affects the growth performance and feed utilization is still confused. miR-34a was reported as a key regulator in the g...

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Autores principales: Miao, Ling-Hong, Lin, Yan, Huang, Xin, Pan, Wen-Jing, Zhou, Qun-Lan, Liu, Bo, Ren, Ming-Chun, Ge, Xian-Ping, Pan, Liang-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121310/
https://www.ncbi.nlm.nih.gov/pubmed/30115855
http://dx.doi.org/10.3390/ijms19082417
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author Miao, Ling-Hong
Lin, Yan
Huang, Xin
Pan, Wen-Jing
Zhou, Qun-Lan
Liu, Bo
Ren, Ming-Chun
Ge, Xian-Ping
Pan, Liang-Kun
author_facet Miao, Ling-Hong
Lin, Yan
Huang, Xin
Pan, Wen-Jing
Zhou, Qun-Lan
Liu, Bo
Ren, Ming-Chun
Ge, Xian-Ping
Pan, Liang-Kun
author_sort Miao, Ling-Hong
collection PubMed
description The Megalobrama amblycephala (M. amblycephala) is one of the most important economic freshwater fish in China. The molecular mechanism under the glucose intolerance responses which affects the growth performance and feed utilization is still confused. miR-34a was reported as a key regulator in the glucose metabolism, but how did the miR-34a exert its function in the metabolism of glucose/insulin in M. amblycephala was still unclear. In this study, we intraperitoneally injected the miR-34a inhibitor (80 nmol/100 g body weight) into M. amblycephala (fed with high starch diet, 45% starch) for 12 h, and then analyzed the gene expression profiling in livers by RNA-seq. The results showed that miR-34a expression in M. amblycephala livers was inhibited by injection of miR-34a inhibitor, and a total of 2212 differentially expressed genes (DEGs) were dysregulated (including 1183 up- and 1029 downregulated DEGs). Function enrichment analysis of DEGs showed that most of them were enriched in the peroxisome proliferator-activated receptor (PPAR), insulin, AMP-activated protein kinase (AMPK) and janus kinase/signal transducers and activators of transcription (JAK/STAT) signaling pathways, which were all associated with the glucose/lipid metabolic and biosynthetic processes. In addition, we examined and verified the differential expression levels of some genes involved in AMPK signaling pathway by qRT-PCR. These results demonstrated that the inhibition of miR-34a might regulate glucose metabolism in M. amblycephala through downstream target genes.
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spelling pubmed-61213102018-09-07 In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala Miao, Ling-Hong Lin, Yan Huang, Xin Pan, Wen-Jing Zhou, Qun-Lan Liu, Bo Ren, Ming-Chun Ge, Xian-Ping Pan, Liang-Kun Int J Mol Sci Article The Megalobrama amblycephala (M. amblycephala) is one of the most important economic freshwater fish in China. The molecular mechanism under the glucose intolerance responses which affects the growth performance and feed utilization is still confused. miR-34a was reported as a key regulator in the glucose metabolism, but how did the miR-34a exert its function in the metabolism of glucose/insulin in M. amblycephala was still unclear. In this study, we intraperitoneally injected the miR-34a inhibitor (80 nmol/100 g body weight) into M. amblycephala (fed with high starch diet, 45% starch) for 12 h, and then analyzed the gene expression profiling in livers by RNA-seq. The results showed that miR-34a expression in M. amblycephala livers was inhibited by injection of miR-34a inhibitor, and a total of 2212 differentially expressed genes (DEGs) were dysregulated (including 1183 up- and 1029 downregulated DEGs). Function enrichment analysis of DEGs showed that most of them were enriched in the peroxisome proliferator-activated receptor (PPAR), insulin, AMP-activated protein kinase (AMPK) and janus kinase/signal transducers and activators of transcription (JAK/STAT) signaling pathways, which were all associated with the glucose/lipid metabolic and biosynthetic processes. In addition, we examined and verified the differential expression levels of some genes involved in AMPK signaling pathway by qRT-PCR. These results demonstrated that the inhibition of miR-34a might regulate glucose metabolism in M. amblycephala through downstream target genes. MDPI 2018-08-16 /pmc/articles/PMC6121310/ /pubmed/30115855 http://dx.doi.org/10.3390/ijms19082417 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Miao, Ling-Hong
Lin, Yan
Huang, Xin
Pan, Wen-Jing
Zhou, Qun-Lan
Liu, Bo
Ren, Ming-Chun
Ge, Xian-Ping
Pan, Liang-Kun
In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala
title In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala
title_full In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala
title_fullStr In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala
title_full_unstemmed In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala
title_short In Vivo Analysis of miR-34a Regulated Glucose Metabolism Related Genes in Megalobrama amblycephala
title_sort in vivo analysis of mir-34a regulated glucose metabolism related genes in megalobrama amblycephala
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121310/
https://www.ncbi.nlm.nih.gov/pubmed/30115855
http://dx.doi.org/10.3390/ijms19082417
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