Some motifs were important for myostatin transcriptional regulation in sheep (Ovis aries).

Rong Du, Xiao-Rong An, Yong-Fu Chen, Jian Qin
{"title":"Some motifs were important for myostatin transcriptional regulation in sheep (Ovis aries).","authors":"Rong Du,&nbsp;Xiao-Rong An,&nbsp;Yong-Fu Chen,&nbsp;Jian Qin","doi":"10.5483/bmbrep.2007.40.4.547","DOIUrl":null,"url":null,"abstract":"<p><p>Many motifs along the 1.2 kb myostatin promoter (MSTNpro) in sheep have been found by the MatInspecter program in our recent study. To further verify the role of the motifs and better understand the transcriptional regulation mechanism of the myostatin gene in sheep, the reporter gene EGFP (enhanced green fluorescent protein) was selected and the wild-type (W) vector MSTNPro(W)-EGFP or motif-mutational (M) vector MSTNPro(M)-EGFP were constructed. The transcriptional regulation activities were analyzed by detecting the fluorescence strength of EGFP in C2C12 myoblasts transfected with the vectors. The results showed that E-box (E) 3, E4, E5 and E7, particularly E3, E5 and E7, had important effects on the activity of the 1.2 kb sheep myostatin promoter. In addition, we also detected several other important motifs such as MTBF (muscle-specific Mt binding factor), MEF2 (myocyte enhancer factor 2), GRE (glucocorticoid response elements) and PRE (progesterone response elements) along the sheep myostatin promoter by the mutational analysis.</p>","PeriodicalId":15113,"journal":{"name":"Journal of biochemistry and molecular biology","volume":"40 4","pages":"547-53"},"PeriodicalIF":0.0000,"publicationDate":"2007-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"40","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biochemistry and molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5483/bmbrep.2007.40.4.547","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 40

Abstract

Many motifs along the 1.2 kb myostatin promoter (MSTNpro) in sheep have been found by the MatInspecter program in our recent study. To further verify the role of the motifs and better understand the transcriptional regulation mechanism of the myostatin gene in sheep, the reporter gene EGFP (enhanced green fluorescent protein) was selected and the wild-type (W) vector MSTNPro(W)-EGFP or motif-mutational (M) vector MSTNPro(M)-EGFP were constructed. The transcriptional regulation activities were analyzed by detecting the fluorescence strength of EGFP in C2C12 myoblasts transfected with the vectors. The results showed that E-box (E) 3, E4, E5 and E7, particularly E3, E5 and E7, had important effects on the activity of the 1.2 kb sheep myostatin promoter. In addition, we also detected several other important motifs such as MTBF (muscle-specific Mt binding factor), MEF2 (myocyte enhancer factor 2), GRE (glucocorticoid response elements) and PRE (progesterone response elements) along the sheep myostatin promoter by the mutational analysis.

一些基序在绵羊(Ovis aries)的肌肉生长抑制素转录调控中很重要。
在我们最近的研究中,MatInspecter程序在绵羊的1.2 kb肌生长抑制素启动子(MSTNpro)上发现了许多基序。为了进一步验证这些基序的作用,更好地了解绵羊肌生长抑制素基因的转录调控机制,我们选择了报告基因EGFP(增强型绿色荧光蛋白),构建了野生型(W)载体MSTNPro(W)-EGFP或基序突变型(M)载体MSTNPro(M)-EGFP。通过检测转染载体的C2C12成肌细胞中EGFP的荧光强度,分析其转录调控活性。结果表明,E-box (E) 3、E4、E5和E7,特别是E3、E5和E7对1.2 kb绵羊肌肉生长抑制素启动子的活性有重要影响。此外,通过突变分析,我们还发现了其他几个重要的基元,如MTBF(肌肉特异性Mt结合因子),MEF2(肌细胞增强因子2),GRE(糖皮质激素反应元件)和PRE(孕酮反应元件)沿着绵羊肌生长抑制素启动子。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信