MMP2 regulates proliferation and differentiation in chicken primary myoblasts, and RNA-seq screens for key genes

IF 2.4 3区 生物学 Q2 GENETICS & HEREDITY Gene Pub Date : 2025-04-05 Epub Date: 2025-01-23 DOI:10.1016/j.gene.2025.149268
Yanxing Wang , Wentao Wang , Bochun Zhang , Bingjie Chen , Haigang Ji , Yufang Niu , Yang Liu , Yihan Liu , Jingqi Wang , Zhuanjian Li , Jiguo Xu
{"title":"MMP2 regulates proliferation and differentiation in chicken primary myoblasts, and RNA-seq screens for key genes","authors":"Yanxing Wang ,&nbsp;Wentao Wang ,&nbsp;Bochun Zhang ,&nbsp;Bingjie Chen ,&nbsp;Haigang Ji ,&nbsp;Yufang Niu ,&nbsp;Yang Liu ,&nbsp;Yihan Liu ,&nbsp;Jingqi Wang ,&nbsp;Zhuanjian Li ,&nbsp;Jiguo Xu","doi":"10.1016/j.gene.2025.149268","DOIUrl":null,"url":null,"abstract":"<div><div>The growth and development of chicken skeletal muscle directly affects chicken meat production, which is very important for broiler industry. <em>Matrix metallopeptidase 2 (</em><strong><em>MMP2)</em></strong> exists in skeletal muscle. However, the underlying regulating of <em>MMP2</em> remain unknown. In this study, <em>MMP2</em> promoted cell proliferation and inhibited cell differentiation after overexpression in chicken primary myoblasts cells (<strong>CPMs</strong>). When <em>MMP2</em> was knocked down, it inhibited CPMs proliferation and promoted cell differentiation. Subsequently, RNA sequencing (<strong>RNA-seq</strong>) and bioinformatics analysis were performed on overexpressing <em>MMP2</em>. We identified 265 up-regulated genes and 229 down-regulated genes. Based on the fragments per kilobase million (<strong>FPKM</strong>) ≥ 10, the retained data were analyzed by Pearson correlation analysis. <em>MMP2</em> was positively correlated with <em>carboxypeptidase M (</em><strong><em>CPM</em></strong><em>)</em>, <em>MSTRG.14120</em> and <em>aldehyde dehydrogenase 1 family member A3 (</em><strong><em>ALDH1A3</em></strong><em>)</em>, and the correlation coefficient was the highest (0.998). <em>MMP2</em> was negatively correlated with <em>hes family bHLH transcription factor 1 (</em><strong><em>HES1</em></strong><em>)</em>, and the correlation coefficient was the highest (0.998). Go term was enriched in cellular components or biogenesis, cellular processes, and cell aggregation. KEGG was significantly enriched to the cancer pathway. qRT-PCR analysis validated the transcriptomic results of RNA-seq. In conclusion, these results provided new insights into the molecular mechanisms by which <em>MMP2</em> affected the proliferation and differentiation of chicken myoblasts.</div></div>","PeriodicalId":12499,"journal":{"name":"Gene","volume":"943 ","pages":"Article 149268"},"PeriodicalIF":2.4000,"publicationDate":"2025-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378111925000563","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/23 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

The growth and development of chicken skeletal muscle directly affects chicken meat production, which is very important for broiler industry. Matrix metallopeptidase 2 (MMP2) exists in skeletal muscle. However, the underlying regulating of MMP2 remain unknown. In this study, MMP2 promoted cell proliferation and inhibited cell differentiation after overexpression in chicken primary myoblasts cells (CPMs). When MMP2 was knocked down, it inhibited CPMs proliferation and promoted cell differentiation. Subsequently, RNA sequencing (RNA-seq) and bioinformatics analysis were performed on overexpressing MMP2. We identified 265 up-regulated genes and 229 down-regulated genes. Based on the fragments per kilobase million (FPKM) ≥ 10, the retained data were analyzed by Pearson correlation analysis. MMP2 was positively correlated with carboxypeptidase M (CPM), MSTRG.14120 and aldehyde dehydrogenase 1 family member A3 (ALDH1A3), and the correlation coefficient was the highest (0.998). MMP2 was negatively correlated with hes family bHLH transcription factor 1 (HES1), and the correlation coefficient was the highest (0.998). Go term was enriched in cellular components or biogenesis, cellular processes, and cell aggregation. KEGG was significantly enriched to the cancer pathway. qRT-PCR analysis validated the transcriptomic results of RNA-seq. In conclusion, these results provided new insights into the molecular mechanisms by which MMP2 affected the proliferation and differentiation of chicken myoblasts.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
MMP2调控鸡原代成肌细胞的增殖和分化,RNA-seq筛选关键基因。
鸡骨骼肌的生长发育直接影响到鸡肉的生产,对肉鸡工业具有重要意义。基质金属肽酶2 (MMP2)存在于骨骼肌中。然而,MMP2的潜在调节机制尚不清楚。在本研究中,MMP2在鸡原代成肌细胞(CPMs)中过表达后促进细胞增殖,抑制细胞分化。当MMP2被敲低时,它抑制CPMs的增殖,促进细胞分化。随后,对过表达的MMP2进行RNA测序(RNA-seq)和生物信息学分析。共鉴定出265个上调基因和229个下调基因。根据每千碱基百万片段数(FPKM) ≥ 10对保留数据进行Pearson相关分析。MMP2与羧肽酶M (CPM)、MSTRG.14120和醛脱氢酶1家族成员A3 (ALDH1A3)呈正相关,相关系数最高(0.998)。MMP2与hes家族bHLH转录因子1 (HES1)呈负相关,相关系数最高(0.998)。Go term在细胞组分或生物发生、细胞过程和细胞聚集中富集。KEGG在癌症通路上显著富集。qRT-PCR分析验证了RNA-seq的转录组学结果。总之,这些结果为MMP2影响鸡成肌细胞增殖和分化的分子机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Gene
Gene 生物-遗传学
CiteScore
6.10
自引率
2.90%
发文量
718
审稿时长
42 days
期刊介绍: Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.
期刊最新文献
The NF-κB–driven inflammatory cascade in ischemic stroke: Linking DAMPs, inflammasomes, and neurovascular dysfunction Hypokalemic periodic paralysis: novel perspectives from genetic mutations to clinical management Integrative assessment of genetic diversity and population structure in palmarosa (Cymbopogon martinii var. motia) using morphological and molecular markers Establishment and characterization of an immortalized porcine gastric epithelial cell line and identification of NPC1 as a key mediator of aflatoxin B1 toxicity Time-resolved transcriptomics of FEN1 knockdown HEK293T cells identifies altered rhythmic gene expression
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1