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MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells

MicroRNAs (miRNAs) are mRNA suppressors that regulate a variety of cellular and physiological processes, including cell proliferation, apoptosis, triglyceride synthesis, fat formation, and lipolysis, by post-transcriptional processing. In previous studies, we isolated and sequenced miRNAs from mamma...

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Autores principales: Liu, Juan, Jiang, Ping, Iqbal, Ambreen, Ali, Shaokat, Gao, Zhen, Pan, Ziyi, Xia, Lixin, Yin, Fuquan, Zhao, Zhihui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027660/
https://www.ncbi.nlm.nih.gov/pubmed/33828164
http://dx.doi.org/10.1038/s41598-021-87139-5
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author Liu, Juan
Jiang, Ping
Iqbal, Ambreen
Ali, Shaokat
Gao, Zhen
Pan, Ziyi
Xia, Lixin
Yin, Fuquan
Zhao, Zhihui
author_facet Liu, Juan
Jiang, Ping
Iqbal, Ambreen
Ali, Shaokat
Gao, Zhen
Pan, Ziyi
Xia, Lixin
Yin, Fuquan
Zhao, Zhihui
author_sort Liu, Juan
collection PubMed
description MicroRNAs (miRNAs) are mRNA suppressors that regulate a variety of cellular and physiological processes, including cell proliferation, apoptosis, triglyceride synthesis, fat formation, and lipolysis, by post-transcriptional processing. In previous studies, we isolated and sequenced miRNAs from mammary epithelial cells from Chinese Holstein cows with high and low milk fat percentages. MiR-485 was one of the significantly differentially expressed miRNAs that were identified. In the present study, the relationship between the candidate target gene DTX4 and miR-485 was validated by bioinformatics and real-time fluorescent quantitative PCR (qRT-PCR) and Western blot (WB) analyses in bovine mammary epithelial cells (bMECs). The results indicated that miR-485 negatively regulated the mRNA expression of the target gene DTX4. Furthermore, an shRNA interference vector for the target gene DTX4 was constructed successfully, and it increased the triglyceride content and reduced the cholesterol content of transfected cells. These results suggest that miR-485 may affect the contents of triglycerides (TGs) and cholesterol (CHOL) by targeting the DTX4 gene. This study indicates that miR-485 has a role in regulating milk fat synthesis and that miR-485 targets the DTX4 gene to regulate lipid metabolism in bMECs. These findings contribute to the understanding of the functional significance of miR-485 in milk fat synthesis.
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spelling pubmed-80276602021-04-08 MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells Liu, Juan Jiang, Ping Iqbal, Ambreen Ali, Shaokat Gao, Zhen Pan, Ziyi Xia, Lixin Yin, Fuquan Zhao, Zhihui Sci Rep Article MicroRNAs (miRNAs) are mRNA suppressors that regulate a variety of cellular and physiological processes, including cell proliferation, apoptosis, triglyceride synthesis, fat formation, and lipolysis, by post-transcriptional processing. In previous studies, we isolated and sequenced miRNAs from mammary epithelial cells from Chinese Holstein cows with high and low milk fat percentages. MiR-485 was one of the significantly differentially expressed miRNAs that were identified. In the present study, the relationship between the candidate target gene DTX4 and miR-485 was validated by bioinformatics and real-time fluorescent quantitative PCR (qRT-PCR) and Western blot (WB) analyses in bovine mammary epithelial cells (bMECs). The results indicated that miR-485 negatively regulated the mRNA expression of the target gene DTX4. Furthermore, an shRNA interference vector for the target gene DTX4 was constructed successfully, and it increased the triglyceride content and reduced the cholesterol content of transfected cells. These results suggest that miR-485 may affect the contents of triglycerides (TGs) and cholesterol (CHOL) by targeting the DTX4 gene. This study indicates that miR-485 has a role in regulating milk fat synthesis and that miR-485 targets the DTX4 gene to regulate lipid metabolism in bMECs. These findings contribute to the understanding of the functional significance of miR-485 in milk fat synthesis. Nature Publishing Group UK 2021-04-07 /pmc/articles/PMC8027660/ /pubmed/33828164 http://dx.doi.org/10.1038/s41598-021-87139-5 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Juan
Jiang, Ping
Iqbal, Ambreen
Ali, Shaokat
Gao, Zhen
Pan, Ziyi
Xia, Lixin
Yin, Fuquan
Zhao, Zhihui
MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
title MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
title_full MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
title_fullStr MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
title_full_unstemmed MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
title_short MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
title_sort mir-485 targets the dtx4 gene to regulate milk fat synthesis in bovine mammary epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027660/
https://www.ncbi.nlm.nih.gov/pubmed/33828164
http://dx.doi.org/10.1038/s41598-021-87139-5
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