Estrogen-induced circFAM171A1 regulates sheep myoblast proliferation through the oar-miR-485-5p/MAPK15/MAPK pathway.

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Runqing Chi, Yufang Liu, Peng Wang, Fan Yang, Xiangyu Wang, Xiaoyun He, Ran Di, Mingxing Chu
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引用次数: 0

Abstract

Estrogen is an important hormone that affects muscle development in female animals. Previous studies have shown that estrogen can protect muscle cells from apoptosis by inhibiting the MAPK signaling pathway. However, the molecular mechanisms by which estrogen-induced MAPK signaling regulates myoblast growth and development remain unclear. In this study, RNA-seq was performed on ovariectomized small-tailed Han (OR-STH) sheep and sham surgery small-tailed Han (STH) sheep to analyze the effects of estrogen on muscle growth and development in female animals. There were 8721 differentially expressed circRNAs (DECs), 143 differentially expressed miRNAs (DEMs) and 2238 differentially expressed mRNAs (DEGs) in the longissimus dorsi between the OR-STH and STH groups. Bioinformatics analysis revealed that the differentially expressed gene MAPK15 was significantly enriched in the MAPK signaling pathway, which is important for muscle development. Therefore, we constructed the ceRNA network circFAM171A1/oar-miR-485-5p/MAPK15 and explored its effect on muscle growth and development. The results of the molecular mechanism experiments indicated that circFAM171A1 can sponge oar-miR-485-5p to regulate MAPK15. The addition of the exogenous hormone estradiol (E2) to sheep myoblasts could induce circFAM171A1, regulate the expression of oar-miR-485-5p and MAPK15, and promote the proliferation of sheep myoblasts. The results showed that MAPK15 and circFAM171A1 significantly promoted the proliferation of myoblasts and inhibited the apoptosis of myoblasts in sheep, whereas oar-miR-485-5p inhibited the expression of MAPK15 and circFAM171A1, inhibited myoblast proliferation and promoted apoptosis. Furthermore, circFAM171A1 attenuated the inhibitory effect of oar-miR-485-5p on myoblasts. In summary, estrogen induced the expression of circFAM171A1 in sheep myoblasts, and circFAM171A1 can act as a sponge for oar-miR-485-5p to promote the expression of the target gene MAPK15 and ultimately regulate the proliferation of sheep myoblasts. This study provides new insights into the molecular mechanism of estrogen regulation of muscle growth and development in female animals.

雌激素诱导的cirfam171a1通过mir -485-5p/MAPK15/MAPK通路调控绵羊成肌细胞增殖。
雌激素是影响雌性动物肌肉发育的重要激素。先前的研究表明,雌激素可以通过抑制MAPK信号通路来保护肌肉细胞免于凋亡。然而,雌激素诱导的MAPK信号调控成肌细胞生长发育的分子机制尚不清楚。本研究通过对去卵巢小尾寒羊(OR-STH)和假手术小尾寒羊(STH)进行RNA-seq分析,分析雌激素对雌性动物肌肉生长发育的影响。OR-STH组和STH组背最长肌中有8721个差异表达的环状rna (DECs), 143个差异表达的mirna (dem)和2238个差异表达的mrna (DEGs)。生物信息学分析显示,MAPK信号通路中差异表达基因MAPK15显著富集,该基因对肌肉发育具有重要意义。因此,我们构建了ceRNA网络circFAM171A1/oar-miR-485-5p/MAPK15,并探讨其在肌肉生长发育中的作用。分子机制实验结果表明circFAM171A1可以海绵浆- mir -485-5p调控MAPK15。在绵羊成肌细胞中添加外源激素雌二醇(E2)可诱导circFAM171A1表达,调节ar- mir -485-5p和MAPK15的表达,促进绵羊成肌细胞的增殖。结果显示,MAPK15和circFAM171A1显著促进绵羊成肌细胞增殖,抑制成肌细胞凋亡,而oar-miR-485-5p抑制MAPK15和circFAM171A1的表达,抑制成肌细胞增殖,促进细胞凋亡。此外,circFAM171A1减弱了ar- mir -485-5p对成肌细胞的抑制作用。综上所述,雌激素诱导circFAM171A1在绵羊成肌细胞中表达,circFAM171A1可以作为mir - mir -485-5p的海绵,促进靶基因MAPK15的表达,最终调控绵羊成肌细胞的增殖。本研究为雌激素调控雌性动物肌肉生长发育的分子机制提供了新的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular and Molecular Life Sciences
Cellular and Molecular Life Sciences 生物-生化与分子生物学
CiteScore
13.20
自引率
1.20%
发文量
546
审稿时长
1.0 months
期刊介绍: Journal Name: Cellular and Molecular Life Sciences (CMLS) Location: Basel, Switzerland Focus: Multidisciplinary journal Publishes research articles, reviews, multi-author reviews, and visions & reflections articles Coverage: Latest aspects of biological and biomedical research Areas include: Biochemistry and molecular biology Cell biology Molecular and cellular aspects of biomedicine Neuroscience Pharmacology Immunology Additional Features: Welcomes comments on any article published in CMLS Accepts suggestions for topics to be covered
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