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A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development

Milk casein and triglyceride content are important production traits in goats. Studies on mechanisms in milk casein secretion and mammary gland development is essential for milk goat breeding. miRNAs play an important role in goat lactation. While novel-miR-3880 is highly expressed at goat peak lact...

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Autores principales: Zhang, Yue, Liu, Jidan, Li, Wenfei, Cao, Fangjun, Niu, Guanglin, Ji, Shengyue, Du, Xiaoyan, Cao, Binyun, An, Xiaopeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325939/
https://www.ncbi.nlm.nih.gov/pubmed/32656203
http://dx.doi.org/10.3389/fcell.2020.00383
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author Zhang, Yue
Liu, Jidan
Li, Wenfei
Cao, Fangjun
Niu, Guanglin
Ji, Shengyue
Du, Xiaoyan
Cao, Binyun
An, Xiaopeng
author_facet Zhang, Yue
Liu, Jidan
Li, Wenfei
Cao, Fangjun
Niu, Guanglin
Ji, Shengyue
Du, Xiaoyan
Cao, Binyun
An, Xiaopeng
author_sort Zhang, Yue
collection PubMed
description Milk casein and triglyceride content are important production traits in goats. Studies on mechanisms in milk casein secretion and mammary gland development is essential for milk goat breeding. miRNAs play an important role in goat lactation. While novel-miR-3880 is highly expressed at goat peak lactation stage, its molecular mechanism has not been studied. The purpose of the present study was to explore the relationship between novel-miR-3880 and lactation, as well as to construct a network among novel-miR-3880, ciRNA13761, and E74 like ETS transcription factor 2 (ELF2), thus further exploring their potential roles in milk components and mammary gland development. ELF2 was previously proven to be important in cell survival and proliferation, and 3′-UTR of ELF2 was predicted to have binding sites of novel-miR-3880. Our study found that the overexpression of novel-miR-3880 exerted anti-apoptotic and proliferative roles in GMEC, induced a boost in triglyceride synthesis, and caused a decrease in α s1-, α s2-, and β-casein, but an increase in κ-casein secretion. Furthermore, treatment in mice indicated that novel-miR-3880 could promote mammary gland development and extend the lactation period, while novel-miR-3880 expression was found to be suppressed by ciRNA13761 as a miRNA sponge. The present study explores a mechanism of triglyceride synthesis and casein secretion, and reveals a crosstalk between ciRNA13761/novel-miR-3880/ELF2 axis and PI3K/AKT/mTOR/S6K1 pathway, to gain a better understanding of lactation traits in dairy goats.
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spelling pubmed-73259392020-07-09 A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development Zhang, Yue Liu, Jidan Li, Wenfei Cao, Fangjun Niu, Guanglin Ji, Shengyue Du, Xiaoyan Cao, Binyun An, Xiaopeng Front Cell Dev Biol Cell and Developmental Biology Milk casein and triglyceride content are important production traits in goats. Studies on mechanisms in milk casein secretion and mammary gland development is essential for milk goat breeding. miRNAs play an important role in goat lactation. While novel-miR-3880 is highly expressed at goat peak lactation stage, its molecular mechanism has not been studied. The purpose of the present study was to explore the relationship between novel-miR-3880 and lactation, as well as to construct a network among novel-miR-3880, ciRNA13761, and E74 like ETS transcription factor 2 (ELF2), thus further exploring their potential roles in milk components and mammary gland development. ELF2 was previously proven to be important in cell survival and proliferation, and 3′-UTR of ELF2 was predicted to have binding sites of novel-miR-3880. Our study found that the overexpression of novel-miR-3880 exerted anti-apoptotic and proliferative roles in GMEC, induced a boost in triglyceride synthesis, and caused a decrease in α s1-, α s2-, and β-casein, but an increase in κ-casein secretion. Furthermore, treatment in mice indicated that novel-miR-3880 could promote mammary gland development and extend the lactation period, while novel-miR-3880 expression was found to be suppressed by ciRNA13761 as a miRNA sponge. The present study explores a mechanism of triglyceride synthesis and casein secretion, and reveals a crosstalk between ciRNA13761/novel-miR-3880/ELF2 axis and PI3K/AKT/mTOR/S6K1 pathway, to gain a better understanding of lactation traits in dairy goats. Frontiers Media S.A. 2020-06-16 /pmc/articles/PMC7325939/ /pubmed/32656203 http://dx.doi.org/10.3389/fcell.2020.00383 Text en Copyright © 2020 Zhang, Liu, Li, Cao, Niu, Ji, Du, Cao and An. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Zhang, Yue
Liu, Jidan
Li, Wenfei
Cao, Fangjun
Niu, Guanglin
Ji, Shengyue
Du, Xiaoyan
Cao, Binyun
An, Xiaopeng
A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development
title A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development
title_full A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development
title_fullStr A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development
title_full_unstemmed A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development
title_short A Regulatory Circuit Orchestrated by Novel-miR-3880 Modulates Mammary Gland Development
title_sort regulatory circuit orchestrated by novel-mir-3880 modulates mammary gland development
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325939/
https://www.ncbi.nlm.nih.gov/pubmed/32656203
http://dx.doi.org/10.3389/fcell.2020.00383
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